Bioconductor Software Packages
Bioconductor version: 3.11
Package | Maintainer | Title |
---|---|---|
a4 | Tobias Verbeke, Laure Cougnaud | Automated Affymetrix Array Analysis Umbrella Package |
a4Base | Tobias Verbeke, Laure Cougnaud | Automated Affymetrix Array Analysis Base Package |
a4Classif | Tobias Verbeke, Laure Cougnaud | Automated Affymetrix Array Analysis Classification Package |
a4Core | Tobias Verbeke, Laure Cougnaud | Automated Affymetrix Array Analysis Core Package |
a4Preproc | Tobias Verbeke, Laure Cougnaud | Automated Affymetrix Array Analysis Preprocessing Package |
a4Reporting | Tobias Verbeke, Laure Cougnaud | Automated Affymetrix Array Analysis Reporting Package |
ABAEnrichment | Steffi Grote | Gene expression enrichment in human brain regions |
ABarray | Yongming Andrew Sun | Microarray QA and statistical data analysis for Applied Biosystems Genome Survey Microrarray (AB1700) gene expression data. |
abseqR | JiaHong Fong | Reporting and data analysis functionalities for Rep-Seq datasets of antibody libraries |
ABSSeq | Wentao Yang | ABSSeq: a new RNA-Seq analysis method based on modelling absolute expression differences |
acde | Juan Pablo Acosta | Artificial Components Detection of Differentially Expressed Genes |
ACE | Jos B Poell | Absolute Copy Number Estimation from Low-coverage Whole Genome Sequencing |
aCGH | Peter Dimitrov | Classes and functions for Array Comparative Genomic Hybridization data |
ACME | Sean Davis | Algorithms for Calculating Microarray Enrichment (ACME) |
ADaCGH2 | Ramon Diaz-Uriarte | Analysis of big data from aCGH experiments using parallel computing and ff objects |
ADAM | Jose Luiz Rybarczyk Filho | ADAM: Activity and Diversity Analysis Module |
ADAMgui | Jose Luiz Rybarczyk Filho | Activity and Diversity Analysis Module Graphical User Interface |
adaptest | Weixin Cai | Data-Adaptive Statistics for High-Dimensional Multiple Testing |
adductomicsR | Josie Hayes | Processing of adductomic mass spectral datasets |
adSplit | Claudio Lottaz | Annotation-Driven Clustering |
AffiXcan | Alessandro Lussana | A Functional Approach To Impute Genetically Regulated Expression |
affxparser | Kasper Daniel Hansen | Affymetrix File Parsing SDK |
affy | Rafael A. Irizarry | Methods for Affymetrix Oligonucleotide Arrays |
affycomp | Rafael A. Irizarry | Graphics Toolbox for Assessment of Affymetrix Expression Measures |
AffyCompatible | Martin Morgan | Affymetrix GeneChip software compatibility |
affyContam | V. Carey | structured corruption of affymetrix cel file data |
affycoretools | James W. MacDonald | Functions useful for those doing repetitive analyses with Affymetrix GeneChips |
AffyExpress | Xuejun Arthur Li | Affymetrix Quality Assessment and Analysis Tool |
affyILM | Myriam Kroll and Fabrice Berger | Linear Model of background subtraction and the Langmuir isotherm |
affyio | Ben Bolstad | Tools for parsing Affymetrix data files |
affylmGUI | Gordon Smyth | GUI for limma Package with Affymetrix Microarrays |
affyPara | Markus Schmidberger | Parallelized preprocessing methods for Affymetrix Oligonucleotide Arrays |
affypdnn | Laurent Gautier | Probe Dependent Nearest Neighbours (PDNN) for the affy package |
affyPLM | Ben Bolstad | Methods for fitting probe-level models |
affyQCReport | Craig Parman | QC Report Generation for affyBatch objects |
AffyRNADegradation | Mario Fasold | Analyze and correct probe positional bias in microarray data due to RNA degradation |
AGDEX | Cuilan lani Gao | Agreement of Differential Expression Analysis |
agilp | Benny Chain | Agilent expression array processing package |
AgiMicroRna | Pedro Lopez-Romero | Processing and Differential Expression Analysis of Agilent microRNA chips |
AIMS | Eric R Paquet | AIMS : Absolute Assignment of Breast Cancer Intrinsic Molecular Subtype |
ALDEx2 | Greg Gloor | Analysis Of Differential Abundance Taking Sample Variation Into Account |
alevinQC | Charlotte Soneson | Generate QC Reports For Alevin Output |
AllelicImbalance | Jesper R Gadin | Investigates Allele Specific Expression |
AlphaBeta | Yadollah Shahryary Dizaji | Computational inference of epimutation rates and spectra from high-throughput DNA methylation data in plants |
alpine | Michael Love | alpine |
ALPS | Venu Thatikonda | AnaLysis routines for ePigenomicS data |
alsace | Ron Wehrens | ALS for the Automatic Chemical Exploration of mixtures |
altcdfenvs | Laurent Gautier | alternative CDF environments (aka probeset mappings) |
AMARETTO | Olivier Gevaert | Regulatory Network Inference and Driver Gene Evaluation using Integrative Multi-Omics Analysis and Penalized Regression |
AMOUNTAIN | Dong Li | Active modules for multilayer weighted gene co-expression networks: a continuous optimization approach |
amplican | Eivind Valen | Automated analysis of CRISPR experiments |
AnalysisPageServer | Brad Friedman | A framework for sharing interactive data and plots from R through the web |
anamiR | Ti-Tai Wang | An integrated analysis package of miRNA and mRNA expression data |
Anaquin | Ted Wong | Statistical analysis of sequins |
AneuFinder | Aaron Taudt | Analysis of Copy Number Variation in Single-Cell-Sequencing Data |
ANF | Tianle Ma | Affinity Network Fusion for Complex Patient Clustering |
animalcules | Yue Zhao | Interactive microbiome analysis toolkit |
annaffy | Colin A. Smith | Annotation tools for Affymetrix biological metadata |
annmap | Chris Wirth | Genome annotation and visualisation package pertaining to Affymetrix arrays and NGS analysis. |
annotate | Bioconductor Package Maintainer | Annotation for microarrays |
AnnotationDbi | Bioconductor Package Maintainer | Manipulation of SQLite-based annotations in Bioconductor |
AnnotationFilter | Bioconductor Package Maintainer | Facilities for Filtering Bioconductor Annotation Resources |
AnnotationForge | Bioconductor Package Maintainer | Tools for building SQLite-based annotation data packages |
AnnotationFuncs | Stefan McKinnon Edwards | Annotation translation functions |
AnnotationHub | Bioconductor Package Maintainer | Client to access AnnotationHub resources |
AnnotationHubData | Bioconductor Package Maintainer | Transform public data resources into Bioconductor Data Structures |
annotationTools | Alexandre Kuhn | Annotate microarrays and perform cross-species gene expression analyses using flat file databases |
annotatr | Raymond G. Cavalcante | Annotation of Genomic Regions to Genomic Annotations |
anota | Ola Larsson | ANalysis Of Translational Activity (ANOTA). |
anota2seq | Christian Oertlin, Julie Lorent | Generally applicable transcriptome-wide analysis of translational efficiency using anota2seq |
antiProfiles | Hector Corrada Bravo | Implementation of gene expression anti-profiles |
AnVIL | Martin Morgan | Bioconductor on the AnVIL compute environment |
APAlyzer | Ruijia Wang | A toolkit for APA analysis using RNA-seq data |
apComplex | Denise Scholtens | Estimate protein complex membership using AP-MS protein data |
apeglm | Anqi Zhu | Approximate posterior estimation for GLM coefficients |
appreci8R | Sarah Sandmann | appreci8R: an R/Bioconductor package for filtering SNVs and short indels with high sensitivity and high PPV |
aroma.light | Henrik Bengtsson | Light-Weight Methods for Normalization and Visualization of Microarray Data using Only Basic R Data Types |
ArrayExpress | Suhaib Mohammed | Access the ArrayExpress Microarray Database at EBI and build Bioconductor data structures: ExpressionSet, AffyBatch, NChannelSet |
ArrayExpressHTS | Angela Goncalves, Andrew Tikhonov | ArrayExpress High Throughput Sequencing Processing Pipeline |
arrayMvout | V. Carey | multivariate outlier detection for expression array QA |
arrayQuality | Agnes Paquet | Assessing array quality on spotted arrays |
arrayQualityMetrics | Mike Smith | Quality metrics report for microarray data sets |
ArrayTools | Arthur Li | geneChip Analysis Package |
ArrayTV | Eitan Halper-Stromberg | Implementation of wave correction for arrays |
ARRmNormalization | Jean-Philippe Fortin | Adaptive Robust Regression normalization for Illumina methylation data |
artMS | David Jimenez-Morales | Analytical R tools for Mass Spectrometry |
ASAFE | Qian Zhang | Ancestry Specific Allele Frequency Estimation |
ASEB | Likun Wang | Predict Acetylated Lysine Sites |
ASGSCA | Hela Romdhani | Association Studies for multiple SNPs and multiple traits using Generalized Structured Equation Models |
ASICS | Gaëlle Lefort | Automatic Statistical Identification in Complex Spectra |
ASpediaFI | Doyeong Yu | ASpedia-FI: Functional Interaction Analysis of Alternative Splicing Events |
ASpli | Estefania Mancini | Analysis of alternative splicing using RNA-Seq |
AssessORF | Deepank Korandla | Assess Gene Predictions Using Proteomics and Evolutionary Conservation |
ASSET | Samsiddhi Bhattacharjee | An R package for subset-based association analysis of heterogeneous traits and subtypes |
ASSIGN | Ying Shen, W. Evan Johnson, David Jenkins, Mumtehena Rahman | Adaptive Signature Selection and InteGratioN (ASSIGN) |
ATACseqQC | Jianhong Ou | ATAC-seq Quality Control |
atSNP | Sunyoung Shin | Affinity test for identifying regulatory SNPs |
attract | Samuel Zimmerman | Methods to Find the Gene Expression Modules that Represent the Drivers of Kauffman's Attractor Landscape |
AUCell | Sara Aibar | AUCell: Analysis of 'gene set' activity in single-cell RNA-seq data (e.g. identify cells with specific gene signatures) |
Autotuner | Craig McLean | Automated parameter selection for untargeted metabolomics data processing |
AWFisher | Zhiguang Huo | An R package for fast computing for adaptively weighted fisher's method |
BaalChIP | Ines de Santiago | BaalChIP: Bayesian analysis of allele-specific transcription factor binding in cancer genomes |
BAC | Raphael Gottardo | Bayesian Analysis of Chip-chip experiment |
bacon | Maarten van Iterson | Controlling bias and inflation in association studies using the empirical null distribution |
BADER | Andreas Neudecker | Bayesian Analysis of Differential Expression in RNA Sequencing Data |
BadRegionFinder | Sarah Sandmann | BadRegionFinder: an R/Bioconductor package for identifying regions with bad coverage |
BAGS | Alejandro Quiroz-Zarate | A Bayesian Approach for Geneset Selection |
ballgown | Jack Fu | Flexible, isoform-level differential expression analysis |
bamsignals | Johannes Helmuth | Extract read count signals from bam files |
BANDITS | Simone Tiberi | BANDITS: Bayesian ANalysis of DIfferenTial Splicing |
banocc | George Weingart, Curtis Huttenhower | Bayesian ANalysis Of Compositional Covariance |
basecallQC | Thomas Carroll | Working with Illumina Basecalling and Demultiplexing input and output files |
BaseSpaceR | Jared O'Connell | R SDK for BaseSpace RESTful API |
Basic4Cseq | Carolin Walter | Basic4Cseq: an R/Bioconductor package for analyzing 4C-seq data |
BASiCS | Catalina Vallejos | Bayesian Analysis of Single-Cell Sequencing data |
BasicSTARRseq | Annika Buerger | Basic peak calling on STARR-seq data |
basilisk | Aaron Lun | Freezing Python Versions Inside Bioconductor Packages |
basilisk.utils | Aaron Lun | Basilisk Installation Utilities |
batchelor | Aaron Lun | Single-Cell Batch Correction Methods |
BatchQC | Solaiappan Manimaran | Batch Effects Quality Control Software |
BayesKnockdown | William Chad Young | BayesKnockdown: Posterior Probabilities for Edges from Knockdown Data |
BayesPeak | Jonathan Cairns | Bayesian Analysis of ChIP-seq Data |
bayNorm | Wenhao Tang | Single-cell RNA sequencing data normalization |
baySeq | Thomas J. Hardcastle | Empirical Bayesian analysis of patterns of differential expression in count data |
BBCAnalyzer | Sarah Sandmann | BBCAnalyzer: an R/Bioconductor package for visualizing base counts |
BCRANK | Adam Ameur | Predicting binding site consensus from ranked DNA sequences |
bcSeq | Jiaxing Lin | Fast Sequence Mapping in High-Throughput shRNA and CRISPR Screens |
BDMMAcorrect | ZHENWEI DAI | Meta-analysis for the metagenomic read counts data from different cohorts |
beachmat | Aaron Lun | Compiling Bioconductor to Handle Each Matrix Type |
beadarray | Mark Dunning | Quality assessment and low-level analysis for Illumina BeadArray data |
beadarraySNP | Jan Oosting | Normalization and reporting of Illumina SNP bead arrays |
BeadDataPackR | Mike Smith | Compression of Illumina BeadArray data |
BEARscc | Benjamin Schuster-Boeckler | BEARscc (Bayesian ERCC Assesstment of Robustness of Single Cell Clusters) |
BEAT | Kemal Akman | BEAT - BS-Seq Epimutation Analysis Toolkit |
BEclear | David Rasp | Correction of batch effects in DNA methylation data |
bgafun | Iain Wallace | BGAfun A method to identify specifity determining residues in protein families |
BgeeCall | Julien Wollbrett | Automatic RNA-Seq present/absent gene expression calls generation |
BgeeDB | Julien Wollbrett, Julien Roux, Andrea Komljenovic, Frederic Bastian | Annotation and gene expression data retrieval from Bgee database. TopAnat, an anatomical entities Enrichment Analysis tool for UBERON ontology |
BGmix | Alex Lewin | Bayesian models for differential gene expression |
bgx | Ernest Turro | Bayesian Gene eXpression |
BHC | Rich Savage | Bayesian Hierarchical Clustering |
BicARE | Pierre Gestraud | Biclustering Analysis and Results Exploration |
BiFET | Ahrim Youn | Bias-free Footprint Enrichment Test |
BiGGR | Anand K. Gavai, Hannes Hettling | Constraint based modeling in R using metabolic reconstruction databases |
bigmelon | Tyler J. Gorrie-Stone | Illumina methylation array analysis for large experiments |
bigmemoryExtras | Peter M. Haverty | An extension of the bigmemory package with added safety, convenience, and a factor class |
bigPint | Lindsay Rutter | Big multivariate data plotted interactively |
bioassayR | Tyler Backman | Cross-target analysis of small molecule bioactivity |
Biobase | Bioconductor Package Maintainer | Biobase: Base functions for Bioconductor |
biobroom | John D. Storey and Andrew J. Bass | Turn Bioconductor objects into tidy data frames |
biobtreeR | Tamer Gur | Using biobtree tool from R |
bioCancer | Karim Mezhoud | Interactive Multi-Omics Cancers Data Visualization and Analysis |
BiocCaseStudies | Bioconductor Package Maintainer | BiocCaseStudies: Support for the Case Studies Monograph |
BiocCheck | Bioconductor Package Maintainer | Bioconductor-specific package checks |
BiocDockerManager | Maintainer | Access Bioconductor docker images |
BiocFileCache | Lori Shepherd | Manage Files Across Sessions |
BiocGenerics | Bioconductor Package Maintainer | S4 generic functions used in Bioconductor |
biocGraph | Florian Hahne | Graph examples and use cases in Bioinformatics |
BiocNeighbors | Aaron Lun | Nearest Neighbor Detection for Bioconductor Packages |
BiocOncoTK | VJ Carey | Bioconductor components for general cancer genomics |
BioCor | Lluís Revilla Sancho | Functional similarities |
BiocParallel | Bioconductor Package Maintainer | Bioconductor facilities for parallel evaluation |
BiocPkgTools | Sean Davis | Collection of simple tools for learning about Bioc Packages |
BiocSet | Kayla Morrell | Representing Different Biological Sets |
BiocSingular | Aaron Lun | Singular Value Decomposition for Bioconductor Packages |
BiocSklearn | VJ Carey | interface to python sklearn via Rstudio reticulate |
BiocStyle | Bioconductor Package Maintainer | Standard styles for vignettes and other Bioconductor documents |
BiocVersion | Bioconductor Package Maintainer | Set the appropriate version of Bioconductor packages |
biocViews | Bioconductor Package Maintainer | Categorized views of R package repositories |
BiocWorkflowTools | Mike Smith | Tools to aid the development of Bioconductor Workflow packages |
bioDist | Bioconductor Package Maintainer | Different distance measures |
biomaRt | Mike Smith | Interface to BioMart databases (i.e. Ensembl) |
biomformat | Paul J. McMurdie | An interface package for the BIOM file format |
BioMM | Junfang Chen | BioMM: Biological-informed Multi-stage Machine learning framework for phenotype prediction using omics data |
BioMVCClass | Elizabeth Whalen | Model-View-Controller (MVC) Classes That Use Biobase |
biomvRCNS | Yang Du | Copy Number study and Segmentation for multivariate biological data |
BioNet | Marcus Dittrich | Routines for the functional analysis of biological networks |
BioNetStat | Vinicius Jardim | Biological Network Analysis |
BioQC | Jitao David Zhang | Detect tissue heterogeneity in expression profiles with gene sets |
BioSeqClass | Li Hong | Classification for Biological Sequences |
biosigner | Philippe Rinaudo, Etienne Thevenot | Signature discovery from omics data |
Biostrings | H. Pagès | Efficient manipulation of biological strings |
biosvd | Anneleen Daemen, Matthew Brauer | Package for high-throughput data processing, outlier detection, noise removal and dynamic modeling |
BioTIP | Zhezhen Wang, X Holly Yang and Yuxi (Jennifer) Sun | BioTIP: An R package for characterization of Biological Tipping-Point |
biotmle | Nima Hejazi | Targeted Learning with Moderated Statistics for Biomarker Discovery |
biovizBase | Michael Lawrence | Basic graphic utilities for visualization of genomic data. |
BiRewire | Andrea Gobbi | High-performing routines for the randomization of a bipartite graph (or a binary event matrix), undirected and directed signed graph preserving degree distribution (or marginal totals) |
birta | Benedikt Zacher, Holger Froehlich | Bayesian Inference of Regulation of Transcriptional Activity |
biscuiteer | "Jacob Morrison" | Convenience Functions for Biscuit |
BiSeq | Katja Hebestreit | Processing and analyzing bisulfite sequencing data |
BitSeq | Antti Honkela, Panagiotis Papastamoulis | Transcript expression inference and differential expression analysis for RNA-seq data |
blacksheepr | RugglesLab | Outlier Analysis for pairwise differential comparison |
blima | Vojtěch Kulvait | Tools for the preprocessing and analysis of the Illumina microarrays on the detector (bead) level |
BLMA | Tin Nguyen | BLMA: A package for bi-level meta-analysis |
bnbc | Kipper Fletez-Brant | Bandwise normalization and batch correction of Hi-C data |
BPRMeth | Chantriolnt-Andreas Kapourani | Model higher-order methylation profiles |
BRAIN | Piotr Dittwald | Baffling Recursive Algorithm for Isotope distributioN calculations |
brainflowprobes | Amanda Price | Plots and annotation for choosing BrainFlow target probe sequence |
BrainStars | Itoshi NIKAIDO | query gene expression data and plots from BrainStars (B*) |
branchpointer | Beth Signal | Prediction of intronic splicing branchpoints |
breakpointR | David Porubsky | Find breakpoints in Strand-seq data |
brendaDb | Yi Zhou | The BRENDA Enzyme Database |
BRGenomics | Mike DeBerardine | Tools for the Efficient Analysis of High-Resolution Genomics Data |
bridge | Raphael Gottardo | Bayesian Robust Inference for Differential Gene Expression |
BridgeDbR | Egon Willighagen | Code for using BridgeDb identifier mapping framework from within R |
BrowserViz | Paul Shannon | BrowserViz: interactive R/browser graphics using websockets and JSON |
BSgenome | H. Pagès | Software infrastructure for efficient representation of full genomes and their SNPs |
bsseq | Kasper Daniel Hansen | Analyze, manage and store bisulfite sequencing data |
BubbleTree | Todd Creasy, Wei Zhu | BubbleTree: an intuitive visualization to elucidate tumoral aneuploidy and clonality in somatic mosaicism using next generation sequencing data |
BufferedMatrix | Ben Bolstad | A matrix data storage object held in temporary files |
BufferedMatrixMethods | Ben Bolstad | Microarray Data related methods that utlize BufferedMatrix objects |
BUMHMM | Alina Selega | Computational pipeline for computing probability of modification from structure probing experiment data |
bumphunter | Rafael A. Irizarry | Bump Hunter |
BUS | Yuanhua Liu | Gene network reconstruction |
BUScorrect | Xiangyu Luo | Batch Effects Correction with Unknown Subtypes |
BUSpaRse | Lambda Moses | kallisto | bustools R utilities |
CAFE | Sander Bollen | Chromosmal Aberrations Finder in Expression data |
CAGEfightR | Malte Thodberg | Analysis of Cap Analysis of Gene Expression (CAGE) data using Bioconductor |
CAGEr | Vanja Haberle, Charles Plessy, Damir Baranasic, Sarvesh Nikumbh | Analysis of CAGE (Cap Analysis of Gene Expression) sequencing data for precise mapping of transcription start sites and promoterome mining |
CALIB | Hui Zhao | Calibration model for estimating absolute expression levels from microarray data |
calm | Kun Liang | Covariate Assisted Large-scale Multiple testing |
CAMERA | Steffen Neumann | Collection of annotation related methods for mass spectrometry data |
CAMTHC | Lulu Chen | Convex Analysis of Mixtures for Tissue Heterogeneity Characterization |
canceR | Karim Mezhoud | A Graphical User Interface for accessing and modeling the Cancer Genomics Data of MSKCC |
cancerclass | Daniel Kosztyla | Development and validation of diagnostic tests from high-dimensional molecular data |
CancerInSilico | Thomas D. Sherman, Elana J. Fertig | An R interface for computational modeling of tumor progression |
CancerMutationAnalysis | Simina M. Boca | Cancer mutation analysis |
CancerSubtypes | Taosheng Xu | Cancer subtypes identification, validation and visualization based on multiple genomic data sets |
CAnD | Caitlin McHugh | Perform Chromosomal Ancestry Differences (CAnD) Analyses |
caOmicsV | Henry Zhang | Visualization of multi-dimentional cancer genomics data |
Cardinal | Kylie A. Bemis | A mass spectrometry imaging toolbox for statistical analysis |
CARNIVAL | Enio Gjerga | A CAusal Reasoning tool for Network Identification (from gene expression data) using Integer VALue programming |
casper | David Rossell | Characterization of Alternative Splicing based on Paired-End Reads |
CATALYST | Helena L. Crowell | Cytometry dATa anALYSis Tools |
Category | Bioconductor Package Maintainer | Category Analysis |
categoryCompare | Robert M. Flight | Meta-analysis of high-throughput experiments using feature annotations |
CausalR | Glyn Bradley, Steven Barrett | Causal network analysis methods |
cbaf | Arman Shahrisa | Automated functions for comparing various omic data from cbioportal.org |
cBioPortalData | Marcel Ramos | Exposes and makes available data from the cBioPortal web resources |
ccfindR | Jun Woo | Cancer Clone Finder |
ccmap | Alex Pickering | Combination Connectivity Mapping |
CCPROMISE | Xueyuan Cao | PROMISE analysis with Canonical Correlation for Two Forms of High Dimensional Genetic Data |
ccrepe | Emma Schwager,Craig Bielski, George Weingart | ccrepe_and_nc.score |
celaref | Sarah Williams | Single-cell RNAseq cell cluster labelling by reference |
celda | Joshua Campbell | CEllular Latent Dirichlet Allocation |
cellbaseR | Mohammed OE Abdallah | Querying annotation data from the high performance Cellbase web |
CellBench | Shian Su | Construct Benchmarks for Single Cell Analysis Methods |
cellGrowth | Julien Gagneur | Fitting cell population growth models |
cellHTS2 | Joseph Barry | Analysis of cell-based screens - revised version of cellHTS |
cellity | Tomislav Ilicic | Quality Control for Single-Cell RNA-seq Data |
CellMapper | Brad Nelms | Predict genes expressed selectively in specific cell types |
CellMixS | Almut Lütge | Evaluate Cellspecific Mixing |
CellNOptR | A.Gabor | Training of boolean logic models of signalling networks using prior knowledge networks and perturbation data |
cellscape | Maia Smith | Explores single cell copy number profiles in the context of a single cell tree |
CellScore | Nancy Mah | Tool for Evaluation of Cell Identity from Transcription Profiles |
CellTrails | Daniel Ellwanger | Reconstruction, visualization and analysis of branching trajectories |
cellTree | David duVerle | Inference and visualisation of Single-Cell RNA-seq data as a hierarchical tree structure |
CEMiTool | Helder Nakaya | Co-expression Modules identification Tool |
ceRNAnetsim | Selcen Ari Yuka | Regulation Simulator of Interaction between miRNA and Competing RNAs (ceRNA) |
CeTF | Carlos Alberto Oliveira de Biagi Junior | Coexpression for Transcription Factors using Regulatory Impact Factors and Partial Correlation and Information Theory analysis |
CexoR | Pedro Madrigal | An R package to uncover high-resolution protein-DNA interactions in ChIP-exo replicates |
CFAssay | Herbert Braselmann | Statistical analysis for the Colony Formation Assay |
CGEN | William Wheeler | An R package for analysis of case-control studies in genetic epidemiology |
CGHbase | Mark van de Wiel | CGHbase: Base functions and classes for arrayCGH data analysis. |
CGHcall | Mark van de Wiel | Calling aberrations for array CGH tumor profiles. |
cghMCR | J. Zhang | Find chromosome regions showing common gains/losses |
CGHnormaliter | Bart P.P. van Houte | Normalization of array CGH data with imbalanced aberrations. |
CGHregions | Sjoerd Vosse | Dimension Reduction for Array CGH Data with Minimal Information Loss. |
ChAMP | Yuan Tian | Chip Analysis Methylation Pipeline for Illumina HumanMethylation450 and EPIC |
CHARGE | Benjamin Mayne | CHARGE: CHromosome Assessment in R from Gene Expression data |
ChemmineOB | Thomas Girke | R interface to a subset of OpenBabel functionalities |
ChemmineR | Thomas Girke | Cheminformatics Toolkit for R |
CHETAH | Jurrian de Kanter | Fast and accurate scRNA-seq cell type identification |
ChIC | Carmen Maria Livi | Quality Control Pipeline for ChIP-Seq Data |
Chicago | Mikhail Spivakov | CHiCAGO: Capture Hi-C Analysis of Genomic Organization |
chimera | Raffaele A Calogero | A package for secondary analysis of fusion products |
chimeraviz | Stian Lågstad | Visualization tools for gene fusions |
ChIPanalyser | Patrick C.N. Martin | ChIPanalyser: Predicting Transcription Factor Binding Sites |
ChIPComp | Li Chen | Quantitative comparison of multiple ChIP-seq datasets |
chipenrich | Raymond G. Cavalcante | Gene Set Enrichment For ChIP-seq Peak Data |
ChIPexoQual | Rene Welch | ChIPexoQual |
ChIPpeakAnno | Lihua Julie Zhu, Jianhong Ou | Batch annotation of the peaks identified from either ChIP-seq, ChIP-chip experiments or any experiments resulted in large number of chromosome ranges |
ChIPQC | Tom Carroll, Rory Stark | Quality metrics for ChIPseq data |
ChIPseeker | Guangchuang Yu | ChIPseeker for ChIP peak Annotation, Comparison, and Visualization |
chipseq | Bioconductor Package Maintainer | chipseq: A package for analyzing chipseq data |
ChIPseqR | Peter Humburg | Identifying Protein Binding Sites in High-Throughput Sequencing Data |
ChIPSeqSpike | Nicolas Descostes | ChIP-Seq data scaling according to spike-in control |
ChIPsim | Peter Humburg | Simulation of ChIP-seq experiments |
ChIPXpress | George Wu | ChIPXpress: enhanced transcription factor target gene identification from ChIP-seq and ChIP-chip data using publicly available gene expression profiles |
chopsticks | Hin-Tak Leung | The 'snp.matrix' and 'X.snp.matrix' Classes |
chroGPS | Oscar Reina | chroGPS2: Generation, visualization and differential analysis of epigenome maps |
chromDraw | Jan Janecka | chromDraw is a R package for drawing the schemes of karyotypes in the linear and circular fashion. |
ChromHeatMap | Tim F. Rayner | Heat map plotting by genome coordinate |
chromPlot | Karen Y. Orostica | Global visualization tool of genomic data |
chromstaR | Aaron Taudt | Combinatorial and Differential Chromatin State Analysis for ChIP-Seq Data |
chromswitch | Selin Jessa | An R package to detect chromatin state switches from epigenomic data |
chromVAR | Alicia Schep | Chromatin Variation Across Regions |
CHRONOS | Panos Balomenos | CHRONOS: A time-varying method for microRNA-mediated sub-pathway enrichment analysis |
cicero | Hannah Pliner | Precict cis-co-accessibility from single-cell chromatin accessibility data |
CINdex | Yuriy Gusev | Chromosome Instability Index |
circRNAprofiler | Simona Aufiero | circRNAprofiler: An R-Based Computational Framework for the Downstream Analysis of Circular RNAs |
cisPath | Likun Wang | Visualization and management of the protein-protein interaction networks. |
CiteFuse | Yingxin Lin | CiteFuse: multi-modal analysis of CITE-seq data |
ClassifyR | Dario Strbenac | A framework for cross-validated classification problems, with applications to differential variability and differential distribution testing |
cleanUpdTSeq | Jianhong Ou ; Lihua Julie Zhu | This package classifies putative polyadenylation sites as true or false/internally oligodT primed |
cleaver | Sebastian Gibb | Cleavage of Polypeptide Sequences |
clippda | Stephen Nyangoma | A package for the clinical proteomic profiling data analysis |
clipper | Paolo Martini | Gene Set Analysis Exploiting Pathway Topology |
cliqueMS | Oriol Senan Campos | Annotation of Isotopes, Adducts and Fragmentation Adducts for in-Source LC/MS Metabolomics Data |
Clomial | Habil Zare | Infers clonal composition of a tumor |
Clonality | Irina Ostrovnaya | Clonality testing |
clonotypeR | Charles Plessy | High throughput analysis of T cell antigen receptor sequences |
clst | Noah Hoffman | Classification by local similarity threshold |
clstutils | Noah Hoffman | Tools for performing taxonomic assignment. |
CluMSID | Tobias Depke | Clustering of MS2 Spectra for Metabolite Identification |
clustComp | Aurora Torrente | Clustering Comparison Package |
clusterExperiment | Elizabeth Purdom | Compare Clusterings for Single-Cell Sequencing |
ClusterJudge | Adrian Pasculescu | Judging Quality of Clustering Methods using Mutual Information |
clusterProfiler | Guangchuang Yu | statistical analysis and visualization of functional profiles for genes and gene clusters |
clusterSeq | Thomas J. Hardcastle | Clustering of high-throughput sequencing data by identifying co-expression patterns |
ClusterSignificance | Jason T Serviss | The ClusterSignificance package provides tools to assess if class clusters in dimensionality reduced data representations have a separation different from permuted data |
clusterStab | James W. MacDonald | Compute cluster stability scores for microarray data |
clustifyr | Rui Fu | Classifier for Single-cell RNA-seq Using Cell Clusters |
CMA | Roman Hornung | Synthesis of microarray-based classification |
cmapR | Ted Natoli | CMap Tools in R |
cn.farms | Andreas Mitterecker | cn.FARMS - factor analysis for copy number estimation |
cn.mops | Gundula Povysil | cn.mops - Mixture of Poissons for CNV detection in NGS data |
CNAnorm | Stefano Berri | A normalization method for Copy Number Aberration in cancer samples |
CNEr | Ge Tan | CNE Detection and Visualization |
CNORdt | A. MacNamara | Add-on to CellNOptR: Discretized time treatments |
CNORfeeder | E.Gjerga | Integration of CellNOptR to add missing links |
CNORfuzzy | T. Cokelaer | Addon to CellNOptR: Fuzzy Logic |
CNORode | Enio Gjerga | ODE add-on to CellNOptR |
CNTools | J. Zhang | Convert segment data into a region by sample matrix to allow for other high level computational analyses. |
CNVfilteR | Jose Marcos Moreno-Cabrera | Identifies false positives of CNV calling tools by using SNV calls |
cnvGSA | Joseph Lugo | Gene Set Analysis of (Rare) Copy Number Variants |
CNVPanelizer | Thomas Wolf | Reliable CNV detection in targeted sequencing applications |
CNVRanger | Ludwig Geistlinger | Summarization and expression/phenotype association of CNV ranges |
CNVrd2 | Hoang Tan Nguyen | CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data. |
CNVtools | Chris Barnes | A package to test genetic association with CNV data |
cobindR | Manuela Benary | Finding Co-occuring motifs of transcription factor binding sites |
CoCiteStats | Bioconductor Package Maintainer | Different test statistics based on co-citation. |
COCOA | John Lawson | Coordinate Covariation Analysis |
codelink | Diego Diez | Manipulation of Codelink microarray data |
CODEX | Yuchao Jiang | A Normalization and Copy Number Variation Detection Method for Whole Exome Sequencing |
coexnet | Juan David Henao | coexnet: An R package to build CO-EXpression NETworks from Microarray Data |
CoGAPS | Elana J. Fertig, Thomas D. Sherman | Coordinated Gene Activity in Pattern Sets |
cogena | Zhilong Jia | co-expressed gene-set enrichment analysis |
coGPS | Yingying Wei | cancer outlier Gene Profile Sets |
COHCAP | Charles Warden | CpG Island Analysis Pipeline for Illumina Methylation Array and Targeted BS-Seq Data |
cola | Zuguang Gu | A Framework for Consensus Partitioning |
combi | Joris Meys | Compositional omics model based visual integration |
coMET | Tiphaine Martin | coMET: visualisation of regional epigenome-wide association scan (EWAS) results and DNA co-methylation patterns |
compartmap | Benjamin Johnson | A/B compartment inference from ATAC-seq and methylation array data |
COMPASS | Greg Finak | Combinatorial Polyfunctionality Analysis of Single Cells |
compcodeR | Charlotte Soneson | RNAseq data simulation, differential expression analysis and performance comparison of differential expression methods |
compEpiTools | Kamal Kishore | Tools for computational epigenomics |
CompGO | Ashley J. Waardenberg | An R pipeline for .bed file annotation, comparing GO term enrichment between gene sets and data visualisation |
ComplexHeatmap | Zuguang Gu | Make Complex Heatmaps |
CONFESS | Diana LOW | Cell OrderiNg by FluorEScence Signal |
consensus | Tim Peters | Cross-platform consensus analysis of genomic measurements via interlaboratory testing method |
ConsensusClusterPlus | Matt Wilkerson | ConsensusClusterPlus |
consensusDE | Ashley J. Waardenberg | RNA-seq analysis using multiple algorithms |
consensusOV | Benjamin Haibe-Kains | Gene expression-based subtype classification for high-grade serous ovarian cancer |
consensusSeekeR | Astrid Deschenes | Detection of consensus regions inside a group of experiences using genomic positions and genomic ranges |
contiBAIT | Kieran O'Neill | Improves Early Build Genome Assemblies using Strand-Seq Data |
conumee | Volker Hovestadt | Enhanced copy-number variation analysis using Illumina DNA methylation arrays |
convert | Yee Hwa (Jean) Yang | Convert Microarray Data Objects |
copa | James W. MacDonald | Functions to perform cancer outlier profile analysis. |
copynumber | Gro Nilsen | Segmentation of single- and multi-track copy number data by penalized least squares regression. |
CopyNumberPlots | Bernat Gel | Create Copy-Number Plots using karyoploteR functionality |
CopywriteR | Oscar Krijgsman | Copy number information from targeted sequencing using off-target reads |
coRdon | Anamaria Elek | Codon Usage Analysis and Prediction of Gene Expressivity |
CoRegFlux | Pauline Trébulle and Mohamed Elati | CoRegFlux |
CoRegNet | Remy Nicolle | CoRegNet : reconstruction and integrated analysis of co-regulatory networks |
CoreGx | Benjamin Haibe-Kains | Classes and Functions to Serve as the Basis for Other 'Gx' Packages |
Cormotif | Yingying Wei | Correlation Motif Fit |
CorMut | Zhenpeng Li | Detect the correlated mutations based on selection pressure |
CORREP | Dongxiao Zhu | Multivariate Correlation Estimator and Statistical Inference Procedures. |
coseq | Andrea Rau | Co-Expression Analysis of Sequencing Data |
cosmiq | David Fischer | cosmiq - COmbining Single Masses Into Quantities |
COSNet | Marco Frasca | Cost Sensitive Network for node label prediction on graphs with highly unbalanced labelings |
CountClust | Kushal Dey | Clustering and Visualizing RNA-Seq Expression Data using Grade of Membership Models |
countsimQC | Charlotte Soneson | Compare Characteristic Features of Count Data Sets |
covEB | C. Pacini | Empirical Bayes estimate of block diagonal covariance matrices |
CoverageView | Ernesto Lowy | Coverage visualization package for R |
covRNA | Lara Urban | Multivariate Analysis of Transcriptomic Data |
cpvSNP | Caitlin McHugh | Gene set analysis methods for SNP association p-values that lie in genes in given gene sets |
cqn | Kasper Daniel Hansen | Conditional quantile normalization |
CRImage | Henrik Failmezger, Yinyin Yuan | CRImage a package to classify cells and calculate tumour cellularity |
CRISPRseek | Lihua Julie Zhu | Design of target-specific guide RNAs in CRISPR-Cas9, genome-editing systems |
crisprseekplus | Alper Kucukural | crisprseekplus |
CrispRVariants | Helen Lindsay | Tools for counting and visualising mutations in a target location |
crlmm | Benilton S Carvalho, Robert Scharpf, Matt Ritchie | Genotype Calling (CRLMM) and Copy Number Analysis tool for Affymetrix SNP 5.0 and 6.0 and Illumina arrays |
CrossICC | Yu Sun | An Interactive Consensus Clustering Framework for Multi-platform Data Analysis |
crossmeta | Alex Pickering | Cross Platform Meta-Analysis of Microarray Data |
CSAR | Jose M Muino | Statistical tools for the analysis of ChIP-seq data |
csaw | Aaron Lun | ChIP-Seq Analysis with Windows |
CSSP | Chandler Zuo | ChIP-Seq Statistical Power |
CSSQ | Fan Lab at Georgia Institute of Technology | Chip-seq Signal Quantifier Pipeline |
ctc | Antoine Lucas | Cluster and Tree Conversion. |
CTDquerier | Carles Hernandez-Ferrer | Package for CTDbase data query, visualization and downstream analysis |
ctgGEM | USD Biomedical Engineering | Generating Tree Hierarchy Visualizations from Gene Expression Data |
cTRAP | Nuno Saraiva-Agostinho | Identification of candidate causal perturbations from differential gene expression data |
ctsGE | Michal Sharabi-Schwager | Clustering of Time Series Gene Expression data |
cummeRbund | Loyal A. Goff | Analysis, exploration, manipulation, and visualization of Cufflinks high-throughput sequencing data. |
customProDB | Xiaojing Wang Bo Wen | Generate customized protein database from NGS data, with a focus on RNA-Seq data, for proteomics search |
CVE | Andreas Mock | Cancer Variant Explorer |
cycle | Matthias Futschik | Significance of periodic expression pattern in time-series data |
cydar | Aaron Lun | Using Mass Cytometry for Differential Abundance Analyses |
CytoDx | Zicheng Hu | Robust prediction of clinical outcomes using cytometry data without cell gating |
cytofast | K.A. Stam | cytofast - A quick visualization and analysis tool for CyTOF data |
cytolib | Mike Jiang, Jake Wagner | C++ infrastructure for representing and interacting with the gated cytometry |
cytomapper | Nils Eling | Visualization of highly multiplexed imaging cytometry data in R |
CytoML | Mike Jiang, Jake Wagner | A GatingML Interface for Cross Platform Cytometry Data Sharing |
dada2 | Benjamin Callahan | Accurate, high-resolution sample inference from amplicon sequencing data |
dagLogo | Jianhong Ou | dagLogo: a Bioconductor package for visualizing conserved amino acid sequence pattern in groups based on probability theory |
daMA | Jobst Landgrebe | Efficient design and analysis of factorial two-colour microarray data |
DAMEfinder | Stephany Orjuela | Finds DAMEs - Differential Allelicly MEthylated regions |
DaMiRseq | Mattia Chiesa | Data Mining for RNA-seq data: normalization, feature selection and classification |
DAPAR | Samuel Wieczorek | Tools for the Differential Analysis of Proteins Abundance with R |
DART | Charles Shijie Zheng | Denoising Algorithm based on Relevance network Topology |
DBChIP | Kun Liang | Differential Binding of Transcription Factor with ChIP-seq |
dcanr | Dharmesh D. Bhuva | Differential co-expression/association network analysis |
dcGSA | Jiehuan sun | Distance-correlation based Gene Set Analysis for longitudinal gene expression profiles |
DChIPRep | Bernd Klaus | DChIPRep - Analysis of chromatin modification ChIP-Seq data with replication |
ddCt | Jitao David Zhang | The ddCt Algorithm for the Analysis of Quantitative Real-Time PCR (qRT-PCR) |
ddPCRclust | Benedikt G. Brink | Clustering algorithm for ddPCR data |
dearseq | Boris P. Hejblum | Differential Expression Analysis for RNA-seq data through a robust variance component test |
debCAM | Lulu Chen | Deconvolution by Convex Analysis of Mixtures |
debrowser | Alper Kucukural | Interactive Differential Expresion Analysis Browser |
DECIPHER | Erik Wright | Tools for curating, analyzing, and manipulating biological sequences |
deco | Francisco Jose Campos Laborie | Decomposing Heterogeneous Cohorts using Omic Data Profiling |
DEComplexDisease | Guofeng Meng | A tool for differential expression analysis and DEGs based investigation to complex diseases by bi-clustering analysis |
decompTumor2Sig | Rosario M. Piro | Decomposition of individual tumors into mutational signatures by signature refitting |
DeconRNASeq | Ting Gong | Deconvolution of Heterogeneous Tissue Samples for mRNA-Seq data |
decontam | Benjamin Callahan | Identify Contaminants in Marker-gene and Metagenomics Sequencing Data |
DEDS | Yuanyuan Xiao | Differential Expression via Distance Summary for Microarray Data |
DeepBlueR | Felipe Albrecht, Markus List | DeepBlueR |
deepSNV | Moritz Gerstung | Detection of subclonal SNVs in deep sequencing data. |
DEFormats | Andrzej Oleś | Differential gene expression data formats converter |
DEGraph | Laurent Jacob | Two-sample tests on a graph |
DEGreport | Lorena Pantano | Report of DEG analysis |
DEGseq | Likun Wang | Identify Differentially Expressed Genes from RNA-seq data |
DelayedArray | Hervé Pagès | A unified framework for working transparently with on-disk and in-memory array-like datasets |
DelayedDataFrame | Qian Liu | Delayed operation on DataFrame using standard DataFrame metaphor |
DelayedMatrixStats | Peter Hickey | Functions that Apply to Rows and Columns of 'DelayedMatrix' Objects |
deltaCaptureC | Michael Shapiro | This Package Discovers Meso-scale Chromatin Remodeling from 3C Data |
deltaGseg | Diana Low | deltaGseg |
DeMAND | Jung Hoon Woo, Mariano Alvarez | DeMAND |
DeMixT | Shaolong Cao, Peng Yang | Cell type-specific deconvolution of heterogeneous tumor samples with two or three components using expression data from RNAseq or microarray platforms |
DEP | Arne Smits | Differential Enrichment analysis of Proteomics data |
DepecheR | Jakob Theorell | Determination of essential phenotypic elements of clusters in high-dimensional entities |
DEqMS | Yafeng Zhu | a tool to perform statistical analysis of differential protein expression for quantitative proteomics data. |
derfinder | Leonardo Collado-Torres | Annotation-agnostic differential expression analysis of RNA-seq data at base-pair resolution via the DER Finder approach |
derfinderHelper | Leonardo Collado-Torres | derfinder helper package |
derfinderPlot | Leonardo Collado-Torres | Plotting functions for derfinder |
DEScan2 | Dario Righelli | Differential Enrichment Scan 2 |
DESeq | Simon Anders | Differential gene expression analysis based on the negative binomial distribution |
DESeq2 | Michael Love | Differential gene expression analysis based on the negative binomial distribution |
DEsingle | Zhun Miao | DEsingle for detecting three types of differential expression in single-cell RNA-seq data |
destiny | Philipp Angerer | Creates diffusion maps |
DEsubs | Aristidis G. Vrahatis, Panos Balomenos | DEsubs: an R package for flexible identification of differentially expressed subpathways using RNA-seq expression experiments |
DEWSeq | Hentze bioinformatics team | Differential Expressed Windows Based on Negative Binomial Distribution |
DEXSeq | Alejandro Reyes | Inference of differential exon usage in RNA-Seq |
dexus | Guenter Klambauer | DEXUS - Identifying Differential Expression in RNA-Seq Studies with Unknown Conditions or without Replicates |
DFP | Rodrigo Alvarez-Glez | Gene Selection |
DIAlignR | Shubham Gupta | Dynamic Programming Based Alignment of MS2 Chromatograms |
DiffBind | Rory Stark | Differential Binding Analysis of ChIP-Seq Peak Data |
diffcoexp | Wenbin Wei | Differential Co-expression Analysis |
diffcyt | Lukas M. Weber | Differential discovery in high-dimensional cytometry via high-resolution clustering |
diffGeneAnalysis | Choudary Jagarlamudi | Performs differential gene expression Analysis |
diffHic | Aaron Lun | Differential Analyis of Hi-C Data |
DiffLogo | Hendrik Treutler | DiffLogo: A comparative visualisation of biooligomer motifs |
diffloop | Caleb Lareau | Identifying differential DNA loops from chromatin topology data |
diffuStats | Sergio Picart-Armada | Diffusion scores on biological networks |
diggit | Mariano J Alvarez | Inference of Genetic Variants Driving Cellular Phenotypes |
Director | Katherine Icay | A dynamic visualization tool of multi-level data |
DirichletMultinomial | Martin Morgan | Dirichlet-Multinomial Mixture Model Machine Learning for Microbiome Data |
discordant | Charlotte Siska | The Discordant Method: A Novel Approach for Differential Correlation |
DiscoRhythm | Matthew Carlucci | Interactive Workflow for Discovering Rhythmicity in Biological Data |
distinct | Simone Tiberi | distinct: a method for differential analyses via hierarchical permutation tests |
dittoSeq | Daniel Bunis | User Friendly Single-Cell and Bulk RNA Sequencing Visualization |
divergence | Wikum Dinalankara, Luigi Marchionni | Divergence: Functionality for assessing omics data by divergence with respect to a baseline |
dks | Jeffrey T. Leek | The double Kolmogorov-Smirnov package for evaluating multiple testing procedures. |
DMCFB | Farhad Shokoohi | Differentially Methylated Cytosines via a Bayesian Functional Approach |
DMCHMM | Farhad Shokoohi | Differentially Methylated CpG using Hidden Markov Model |
DMRcaller | Nicolae Radu Zabet | Differentially Methylated Regions caller |
DMRcate | Tim Peters | Methylation array and sequencing spatial analysis methods |
DMRforPairs | Martin Rijlaarsdam | DMRforPairs: identifying Differentially Methylated Regions between unique samples using array based methylation profiles |
DMRScan | Christian M Page | Detection of Differentially Methylated Regions |
dmrseq | Keegan Korthauer | Detection and inference of differentially methylated regions from Whole Genome Bisulfite Sequencing |
DNABarcodeCompatibility | Céline Trébeau | A Tool for Optimizing Combinations of DNA Barcodes Used in Multiplexed Experiments on Next Generation Sequencing Platforms |
DNABarcodes | Tilo Buschmann | A tool for creating and analysing DNA barcodes used in Next Generation Sequencing multiplexing experiments |
DNAcopy | Venkatraman E. Seshan | DNA copy number data analysis |
DNAshapeR | Tsu-Pei Chiu | High-throughput prediction of DNA shape features |
DominoEffect | Marija Buljan, Peter Blattmann | Identification and Annotation of Protein Hotspot Residues |
doppelgangR | Levi Waldron | Identify likely duplicate samples from genomic or meta-data |
Doscheda | Bruno Contrino | A DownStream Chemo-Proteomics Analysis Pipeline |
DOSE | Guangchuang Yu | Disease Ontology Semantic and Enrichment analysis |
doseR | ake.vastermark | doseR |
dpeak | Dongjun Chung | dPeak (Deconvolution of Peaks in ChIP-seq Analysis) |
drawProteins | Paul Brennan | Package to Draw Protein Schematics from Uniprot API output |
DRIMSeq | Malgorzata Nowicka | Differential transcript usage and tuQTL analyses with Dirichlet-multinomial model in RNA-seq |
DriverNet | Jiarui Ding | Drivernet: uncovering somatic driver mutations modulating transcriptional networks in cancer |
DropletUtils | Aaron Lun | Utilities for Handling Single-Cell Droplet Data |
DrugVsDisease | j. Saez-Rodriguez | Comparison of disease and drug profiles using Gene set Enrichment Analysis |
DSS | Hao Wu, Hao Feng | Dispersion shrinkage for sequencing data |
DTA | Bjoern Schwalb | Dynamic Transcriptome Analysis |
dualKS | Eric J. Kort, Yarong Yang | Dual KS Discriminant Analysis and Classification |
Dune | Hector Roux de Bezieux | Improving replicability in single-cell RNA-Seq cell type discovery |
DupChecker | "Quanhu SHENG" | a package for checking high-throughput genomic data redundancy in meta-analysis |
dupRadar | Sergi Sayols, Holger Klein | Assessment of duplication rates in RNA-Seq datasets |
dyebias | Philip Lijnzaad | The GASSCO method for correcting for slide-dependent gene-specific dye bias |
DynDoc | Bioconductor Package Maintainer | Dynamic document tools |
EasyqpcR | Le Pape Sylvain | EasyqpcR for low-throughput real-time quantitative PCR data analysis |
easyreporting | Dario Righelli | Helps creating report for improving Reproducible computational Research |
easyRNASeq | Nicolas Delhomme | Count summarization and normalization for RNA-Seq data |
EBarrays | Ming Yuan | Unified Approach for Simultaneous Gene Clustering and Differential Expression Identification |
EBcoexpress | John A. Dawson | EBcoexpress for Differential Co-Expression Analysis |
EBImage | Andrzej Oleś | Image processing and analysis toolbox for R |
EBSEA | Arfa Mehmood | Exon Based Strategy for Expression Analysis of genes |
EBSeq | Ning Leng | An R package for gene and isoform differential expression analysis of RNA-seq data |
EBSeqHMM | Ning Leng | Bayesian analysis for identifying gene or isoform expression changes in ordered RNA-seq experiments |
ecolitk | Laurent Gautier | Meta-data and tools for E. coli |
EDASeq | Davide Risso | Exploratory Data Analysis and Normalization for RNA-Seq |
EDDA | Chia Kuan Hui Burton, Niranjan Nagarajan | Experimental Design in Differential Abundance analysis |
edge | John D. Storey, Andrew J. Bass | Extraction of Differential Gene Expression |
edgeR | Yunshun Chen, Gordon Smyth, Aaron Lun, Mark Robinson | Empirical Analysis of Digital Gene Expression Data in R |
eegc | Xiaoyuan Zhou | Engineering Evaluation by Gene Categorization (eegc) |
EGAD | Sara Ballouz | Extending guilt by association by degree |
EGSEA | Monther Alhamdoosh | Ensemble of Gene Set Enrichment Analyses |
eiR | Thomas Girke | Accelerated similarity searching of small molecules |
eisa | Gabor Csardi | Expression data analysis via the Iterative Signature Algorithm |
eisaR | Michael Stadler | Exon-Intron Split Analysis (EISA) in R |
ELBOW | Graham Alvare, Xiangli Zhang | ELBOW - Evaluating foLd change By the lOgit Way |
ELMER | Tiago Chedraoui Silva | Inferring Regulatory Element Landscapes and Transcription Factor Networks Using Cancer Methylomes |
EMDomics | Sadhika Malladi and Daniel Schmolze | Earth Mover's Distance for Differential Analysis of Genomics Data |
EmpiricalBrownsMethod | David Gibbs | Uses Brown's method to combine p-values from dependent tests |
ENCODExplorer | Charles Joly Beauparlant | A compilation of ENCODE metadata |
EnhancedVolcano | Kevin Blighe | Publication-ready volcano plots with enhanced colouring and labeling |
EnMCB | Xin Yu | Predicting Disease Progression Based on Methylation Correlated Blocks using Ensemble Models |
ENmix | Zongli Xu | Data preprocessing and quality control for Illumina HumanMethylation450 and MethylationEPIC BeadChip |
EnrichedHeatmap | Zuguang Gu | Making Enriched Heatmaps |
EnrichmentBrowser | Ludwig Geistlinger | Seamless navigation through combined results of set-based and network-based enrichment analysis |
enrichplot | Guangchuang Yu | Visualization of Functional Enrichment Result |
enrichTF | Zheng Wei | Transcription Factors Enrichment Analysis |
ensembldb | Johannes Rainer | Utilities to create and use Ensembl-based annotation databases |
ensemblVEP | Bioconductor Package Maintainer | R Interface to Ensembl Variant Effect Predictor |
ENVISIONQuery | Alex Lisovich, Roger Day | Retrieval from the ENVISION bioinformatics data portal into R |
EpiDISH | Shijie Charles Zheng | Epigenetic Dissection of Intra-Sample-Heterogeneity |
epigenomix | Hans-Ulrich Klein | Epigenetic and gene transcription data normalization and integration with mixture models |
epihet | Xiaowen Chen | Determining Epigenetic Heterogeneity from Bisulfite Sequencing Data |
epiNEM | Martin Pirkl | epiNEM |
EpiTxDb | Felix G.M. Ernst | Storing and accessing epitranscriptomic information using the AnnotationDbi interface |
epivizr | Hector Corrada Bravo | R Interface to epiviz web app |
epivizrChart | Hector Corrada Bravo | R interface to epiviz web components |
epivizrData | Hector Corrada Bravo | Data Management API for epiviz interactive visualization app |
epivizrServer | Hector Corrada Bravo | WebSocket server infrastructure for epivizr apps and packages |
epivizrStandalone | Hector Corrada Bravo | Run Epiviz Interactive Genomic Data Visualization App within R |
erccdashboard | Sarah Munro | Assess Differential Gene Expression Experiments with ERCC Controls |
erma | VJ Carey | epigenomic road map adventures |
ERSSA | Zixuan Shao | Empirical RNA-seq Sample Size Analysis |
esATAC | Zheng Wei | An Easy-to-use Systematic pipeline for ATACseq data analysis |
esetVis | Laure Cougnaud | Visualizations of expressionSet Bioconductor object |
eudysbiome | Xiaoyuan Zhou | Cartesian plot and contingency test on 16S Microbial data |
evaluomeR | José Antonio Bernabé-Díaz | Evaluation of Bioinformatics Metrics |
EventPointer | Juan Pablo Romero | An effective identification of alternative splicing events using junction arrays and RNA-Seq data |
ExCluster | R. Matthew Tanner | ExCluster robustly detects differentially expressed exons between two conditions of RNA-seq data, requiring at least two independent biological replicates per condition |
ExiMiR | Sylvain Gubian | R functions for the normalization of Exiqon miRNA array data |
exomeCopy | Michael Love | Copy number variant detection from exome sequencing read depth |
exomePeak2 | Zhen Wei | Bias Awared Peak Calling and Quantification for MeRIP-Seq |
ExperimentHub | Bioconductor Package Maintainer | Client to access ExperimentHub resources |
ExperimentHubData | Bioconductor Package Maintainer | Add resources to ExperimentHub |
explorase | Michael Lawrence | GUI for exploratory data analysis of systems biology data |
ExploreModelMatrix | Charlotte Soneson | Graphical Exploration of Design Matrices |
ExpressionAtlas | Suhaib Mohammed | Download datasets from EMBL-EBI Expression Atlas |
ExpressionView | Gabor Csardi | Visualize biclusters identified in gene expression data |
fabia | Andreas Mitterecker | FABIA: Factor Analysis for Bicluster Acquisition |
factDesign | Denise Scholtens | Factorial designed microarray experiment analysis |
FamAgg | Johannes Rainer | Pedigree Analysis and Familial Aggregation |
farms | Djork-Arne Clevert | FARMS - Factor Analysis for Robust Microarray Summarization |
fastLiquidAssociation | Tina Gunderson | functions for genome-wide application of Liquid Association |
FastqCleaner | Leandro Roser | A Shiny Application for Quality Control, Filtering and Trimming of FASTQ Files |
fastseg | Guenter Klambauer | fastseg - a fast segmentation algorithm |
FCBF | Tiago Lubiana | Fast Correlation Based Filter for Feature Selection |
fCCAC | Pedro Madrigal | functional Canonical Correlation Analysis to evaluate Covariance between nucleic acid sequencing datasets |
fCI | Shaojun Tang | f-divergence Cutoff Index for Differential Expression Analysis in Transcriptomics and Proteomics |
fcoex | Tiago Lubiana | FCBF-based Co-Expression Networks for Single Cells |
fcScan | Pierre Khoueiry Abdallah El-Kurdi | fcScan for detecting clusters of coordinates with user defined options |
fdrame | Effi Kenigsberg | FDR adjustments of Microarray Experiments (FDR-AME) |
FELLA | Sergio Picart-Armada | Interpretation and enrichment for metabolomics data |
FEM | Zhen Yang | Identification of Functional Epigenetic Modules |
ffpe | Levi Waldron | Quality assessment and control for FFPE microarray expression data |
FGNet | Sara Aibar | Functional Gene Networks derived from biological enrichment analyses |
fgsea | Alexey Sergushichev | Fast Gene Set Enrichment Analysis |
FindMyFriends | Thomas Lin Pedersen | Microbial Comparative Genomics in R |
FISHalyseR | Karesh Arunakirinathan, Andreas Heindl | FISHalyseR a package for automated FISH quantification |
fishpond | Michael Love | Fishpond: differential transcript and gene expression with inferential replicates |
FitHiC | Ruyu Tan | Confidence estimation for intra-chromosomal contact maps |
flagme | Mark Robinson, Riccardo Romoli | Analysis of Metabolomics GC/MS Data |
flowAI | Gianni Monaco | Automatic and interactive quality control for flow cytometry data |
flowBeads | Nikolas Pontikos | flowBeads: Analysis of flow bead data |
flowBin | Kieran O'Neill | Combining multitube flow cytometry data by binning |
flowcatchR | Federico Marini | Tools to analyze in vivo microscopy imaging data focused on tracking flowing blood cells |
flowCHIC | Author: Joachim Schumann | Analyze flow cytometric data using histogram information |
flowCL | Justin Meskas | Semantic labelling of flow cytometric cell populations |
flowClean | Kipper Fletez-Brant | flowClean |
flowClust | Greg Finak, Mike Jiang, Jake Wagner | Clustering for Flow Cytometry |
flowCore | Mike Jiang, Jake Wagner | flowCore: Basic structures for flow cytometry data |
flowCyBar | Joachim Schumann | Analyze flow cytometric data using gate information |
flowDensity | Mehrnoush Malek | Sequential Flow Cytometry Data Gating |
flowFit | Davide Rambaldi | Estimate proliferation in cell-tracking dye studies |
flowFP | Herb Holyst | Fingerprinting for Flow Cytometry |
flowMap | Chiaowen Joyce Hsiao | Mapping cell populations in flow cytometry data for cross-sample comparisons using the Friedman-Rafsky Test |
flowMatch | Ariful Azad | Matching and meta-clustering in flow cytometry |
flowMeans | Nima Aghaeepour | Non-parametric Flow Cytometry Data Gating |
flowMerge | Greg Finak | Cluster Merging for Flow Cytometry Data |
flowPeaks | Yongchao Ge | An R package for flow data clustering |
flowPloidy | Tyler Smith | Analyze flow cytometer data to determine sample ploidy |
flowPlots | N. Hawkins | flowPlots: analysis plots and data class for gated flow cytometry data |
FlowRepositoryR | Josef Spidlen | FlowRepository R Interface |
FlowSOM | Sofie Van Gassen | Using self-organizing maps for visualization and interpretation of cytometry data |
flowSpecs | Jakob Theorell | Tools for processing of high-dimensional cytometry data |
flowSpy | Yuting Dai | A Toolkit for Flow And Mass Cytometry Data |
flowStats | Greg Finak, Mike Jiang, Jake Wagner | Statistical methods for the analysis of flow cytometry data |
flowTime | R. Clay Wright | Annotation and analysis of biological dynamical systems using flow cytometry |
flowTrans | Greg Finak | Parameter Optimization for Flow Cytometry Data Transformation |
flowType | Nima Aghaeepour | Phenotyping Flow Cytometry Assays |
flowUtils | Josef Spidlen | Utilities for flow cytometry |
flowViz | Mike Jiang, Jake Wagner | Visualization for flow cytometry |
flowVS | Ariful Azad | Variance stabilization in flow cytometry (and microarrays) |
flowWorkspace | Greg Finak,Mike Jiang,Jake Wagner | Infrastructure for representing and interacting with gated and ungated cytometry data sets. |
fmcsR | Thomas Girke | Mismatch Tolerant Maximum Common Substructure Searching |
focalCall | Oscar Krijgsman | Detection of focal aberrations in DNA copy number data |
FoldGO | Daniil Wiebe | Package for Fold-specific GO Terms Recognition |
FourCSeq | Mike Smith | Package analyse 4C sequencing data |
FRASER | Christian Mertes | Find RAre Splicing Events in RNA-Seq Data |
frenchFISH | Adam Berman | Poisson Models for Quantifying DNA Copy-number from FISH Images of Tissue Sections |
FRGEpistasis | Futao Zhang | Epistasis Analysis for Quantitative Traits by Functional Regression Model |
frma | Matthew N. McCall | Frozen RMA and Barcode |
frmaTools | Matthew N. McCall | Frozen RMA Tools |
FunChIP | Alice Parodi | Clustering and Alignment of ChIP-Seq peaks based on their shapes |
FunciSNP | Simon G. Coetzee | Integrating Functional Non-coding Datasets with Genetic Association Studies to Identify Candidate Regulatory SNPs |
funtooNorm | Kathleen Klein | Normalization Procedure for Infinium HumanMethylation450 BeadChip Kit |
GA4GHclient | Welliton Souza | A Bioconductor package for accessing GA4GH API data servers |
GA4GHshiny | Welliton Souza | Shiny application for interacting with GA4GH-based data servers |
gaga | David Rossell | GaGa hierarchical model for high-throughput data analysis |
gage | Weijun Luo | Generally Applicable Gene-set Enrichment for Pathway Analysis |
gaggle | Christopher Bare | Broadcast data between R and Gaggle |
gaia | S. Morganella | GAIA: An R package for genomic analysis of significant chromosomal aberrations. |
GAPGOM | Casper van Mourik | GAPGOM (novel Gene Annotation Prediction and other GO Metrics) |
GAprediction | Jon Bohlin | Prediction of gestational age with Illumina HumanMethylation450 data |
garfield | Valentina Iotchkova | GWAS Analysis of Regulatory or Functional Information Enrichment with LD correction |
GARS | Mattia Chiesa | GARS: Genetic Algorithm for the identification of Robust Subsets of variables in high-dimensional and challenging datasets |
GateFinder | Nima Aghaeepour | Projection-based Gating Strategy Optimization for Flow and Mass Cytometry |
gcapc | Mingxiang Teng | GC Aware Peak Caller |
gcatest | Wei Hao, John D. Storey | Genotype Conditional Association TEST |
gCMAP | Thomas Sandmann | Tools for Connectivity Map-like analyses |
gCMAPWeb | Thomas Sandmann | A web interface for gene-set enrichment analyses |
gCrisprTools | Russell Bainer | Suite of Functions for Pooled Crispr Screen QC and Analysis |
gcrma | Z. Wu | Background Adjustment Using Sequence Information |
GCSConnection | Jiefei Wang | Creating R Connection with Google Cloud Storage |
GCSscore | Guy M. Harris | GCSscore: an R package for microarray analysis for Affymetrix/Thermo Fisher arrays |
GDCRNATools | Ruidong Li, Han Qu | GDCRNATools: an R/Bioconductor package for integrative analysis of lncRNA, mRNA, and miRNA data in GDC |
GDSArray | Qian Liu | Representing GDS files as array-like objects |
gdsfmt | Xiuwen Zheng | R Interface to CoreArray Genomic Data Structure (GDS) Files |
geecc | Markus Boenn | Gene Set Enrichment Analysis Extended to Contingency Cubes |
GEM | Hong Pan | GEM: fast association study for the interplay of Gene, Environment and Methylation |
gemini | Sidharth Jain | GEMINI: Variational inference approach to infer genetic interactions from pairwise CRISPR screens |
genArise | IFC Development Team | Microarray Analysis tool |
genbankr | Gabriel Becker | Parsing GenBank files into semantically useful objects |
GeneAccord | Ariane L. Moore | Detection of clonally exclusive gene or pathway pairs in a cohort of cancer patients |
GeneAnswers | Lei Huang and Gang Feng | Integrated Interpretation of Genes |
geneAttribution | Arthur Wuster | Identification of candidate genes associated with genetic variation |
GeneBreak | Evert van den Broek | Gene Break Detection |
geneClassifiers | R Kuiper | Application of gene classifiers |
GeneExpressionSignature | Yang Cao, Fei Li,Lu Han | Gene Expression Signature based Similarity Metric |
genefilter | Bioconductor Package Maintainer | genefilter: methods for filtering genes from high-throughput experiments |
genefu | Benjamin Haibe-Kains | Computation of Gene Expression-Based Signatures in Breast Cancer |
GeneGA | Zhenpeng Li | Design gene based on both mRNA secondary structure and codon usage bias using Genetic algorithm |
GeneGeneInteR | Mathieu Emily, Magalie Houee-Bigot | Tools for Testing Gene-Gene Interaction at the Gene Level |
GeneMeta | Bioconductor Package Maintainer | MetaAnalysis for High Throughput Experiments |
GeneNetworkBuilder | Jianhong Ou | GeneNetworkBuilder: a bioconductor package for building regulatory network using ChIP-chip/ChIP-seq data and Gene Expression Data |
GeneOverlap | Li Shen, Mount Sinai | Test and visualize gene overlaps |
geneplast | Mauro Castro | Evolutionary and plasticity analysis of orthologous groups |
geneplotter | Bioconductor Package Maintainer | Graphics related functions for Bioconductor |
geneRecommender | Greg Hather | A gene recommender algorithm to identify genes coexpressed with a query set of genes |
GeneRegionScan | Lasse Folkersen | GeneRegionScan |
geneRxCluster | Charles Berry | gRx Differential Clustering |
GeneSelectMMD | Weiliang Qiu | Gene selection based on the marginal distributions of gene profiles that characterized by a mixture of three-component multivariate distributions |
GENESIS | Stephanie M. Gogarten | GENetic EStimation and Inference in Structured samples (GENESIS): Statistical methods for analyzing genetic data from samples with population structure and/or relatedness |
GeneStructureTools | Beth Signal | Tools for spliced gene structure manipulation and analysis |
geNetClassifier | Sara Aibar | Classify diseases and build associated gene networks using gene expression profiles |
GeneticsDesign | The R Genetics Project | Functions for designing genetics studies |
GeneticsPed | David Henderson | Pedigree and genetic relationship functions |
GeneTonic | Federico Marini | Enjoy Analyzing And Integrating The Results From Differential Expression Analysis And Functional Enrichment Analysis |
geneXtendeR | Bohdan Khomtchouk | Optimized Functional Annotation Of ChIP-seq Data |
GENIE3 | Van Anh Huynh-Thu | GEne Network Inference with Ensemble of trees |
genoCN | Wei Sun | genotyping and copy number study tools |
GenoGAM | Georg Stricker | A GAM based framework for analysis of ChIP-Seq data |
genomation | Altuna Akalin, Vedran Franke, Katarzyna Wreczycka | Summary, annotation and visualization of genomic data |
GenomeInfoDb | Bioconductor Package Maintainer | Utilities for manipulating chromosome names, including modifying them to follow a particular naming style |
genomeIntervals | Julien Gagneur | Operations on genomic intervals |
genomes | Chris Stubben | Genome sequencing project metadata |
GenomicAlignments | Bioconductor Package Maintainer | Representation and manipulation of short genomic alignments |
GenomicDataCommons | Sean Davis | NIH / NCI Genomic Data Commons Access |
GenomicFeatures | Bioconductor Package Maintainer | Conveniently import and query gene models |
GenomicFiles | Bioconductor Package Maintainer | Distributed computing by file or by range |
GenomicInteractions | Liz Ing-Simmons | Utilities for handling genomic interaction data |
GenomicOZone | Hua Zhong, Mingzhou Song | Delineate outstanding genomic zones of differential gene activity |
GenomicRanges | Bioconductor Package Maintainer | Representation and manipulation of genomic intervals |
GenomicScores | Robert Castelo | Infrastructure to work with genomewide position-specific scores |
GenomicTuples | Peter Hickey | Representation and Manipulation of Genomic Tuples |
Genominator | James Bullard | Analyze, manage and store genomic data |
genoset | Peter M. Haverty | A RangedSummarizedExperiment with methods for copy number analysis |
genotypeeval | Jennifer Tom | QA/QC of a gVCF or VCF file |
genphen | Simo Kitanovski | A tool for quantification of associations between genotypes and phenotypes in genome wide association studies (GWAS) with Bayesian inference and statistical learning |
GenRank | Chakravarthi Kanduri | Candidate gene prioritization based on convergent evidence |
GenVisR | Zachary Skidmore | Genomic Visualizations in R |
GEOmetadb | Jack Zhu | A compilation of metadata from NCBI GEO |
GEOquery | Sean Davis | Get data from NCBI Gene Expression Omnibus (GEO) |
GEOsubmission | Alexandre Kuhn | Prepares microarray data for submission to GEO |
gep2pep | Francesco Napolitano | Creation and Analysis of Pathway Expression Profiles (PEPs) |
gespeR | Fabian Schmich | Gene-Specific Phenotype EstimatoR |
GEWIST | Wei Q. Deng | Gene Environment Wide Interaction Search Threshold |
GGBase | VJ Carey | GGBase infrastructure for genetics of gene expression package GGtools |
ggbio | Michael Lawrence | Visualization tools for genomic data |
ggcyto | Mike Jiang,Jake Wagner | Visualize Cytometry data with ggplot |
GGPA | Dongjun Chung | graph-GPA: A graphical model for prioritizing GWAS results and investigating pleiotropic architecture |
GGtools | VJ Carey | software and data for analyses in genetics of gene expression |
ggtree | Guangchuang Yu | an R package for visualization of tree and annotation data |
GIGSEA | Shijia Zhu | Genotype Imputed Gene Set Enrichment Analysis |
girafe | J. Toedling | Genome Intervals and Read Alignments for Functional Exploration |
GISPA | Bhakti Dwivedi | GISPA: Method for Gene Integrated Set Profile Analysis |
GLAD | Philippe Hupe | Gain and Loss Analysis of DNA |
GladiaTOX | PMP S.A. R Support | R Package for Processing High Content Screening data |
Glimma | Shian Su | Interactive HTML graphics |
glmGamPoi | Constantin Ahlmann-Eltze | Fit a Gamma-Poisson Generalized Linear Model |
glmSparseNet | André Veríssimo | Network Centrality Metrics for Elastic-Net Regularized Models |
GlobalAncova | Manuela Hummel | Global test for groups of variables via model comparisons |
globalSeq | Armin Rauschenberger | Global Test for Counts |
globaltest | Jelle Goeman | Testing Groups of Covariates/Features for Association with a Response Variable, with Applications to Gene Set Testing |
gmapR | Michael Lawrence | An R interface to the GMAP/GSNAP/GSTRUCT suite |
GmicR | Richard Virgen-Slane | Combines WGCNA and xCell readouts with bayesian network learrning to generate a Gene-Module Immune-Cell network (GMIC) |
gmoviz | Kathleen Zeglinski | Seamless visualization of complex genomic variations in GMOs and edited cell lines |
GMRP | Yuan-De Tan | GWAS-based Mendelian Randomization and Path Analyses |
GNET2 | Chen Chen | Constructing gene regulatory networks from expression data through functional module inference |
GOexpress | Kevin Rue-Albrecht | Visualise microarray and RNAseq data using gene ontology annotations |
GOfuncR | Steffi Grote | Gene ontology enrichment using FUNC |
GOFunction | Jing Wang | GO-function: deriving biologcially relevant functions from statistically significant functions |
GOpro | Lidia Chrabaszcz | Find the most characteristic gene ontology terms for groups of human genes |
goProfiles | Alex Sanchez | goProfiles: an R package for the statistical analysis of functional profiles |
GOSemSim | Guangchuang Yu | GO-terms Semantic Similarity Measures |
goseq | Matthew Young, Nadia Davidson | Gene Ontology analyser for RNA-seq and other length biased data |
GOSim | Holger Froehlich | Computation of functional similarities between GO terms and gene products; GO enrichment analysis |
goSTAG | Brian D. Bennett | A tool to use GO Subtrees to Tag and Annotate Genes within a set |
GOstats | Bioconductor Package Maintainer | Tools for manipulating GO and microarrays |
GOsummaries | Raivo Kolde | Word cloud summaries of GO enrichment analysis |
GOTHiC | Borbala Mifsud | Binomial test for Hi-C data analysis |
goTools | Agnes Paquet | Functions for Gene Ontology database |
GPA | Dongjun Chung | GPA (Genetic analysis incorporating Pleiotropy and Annotation) |
gpart | Sun Ah Kim | Human genome partitioning of dense sequencing data by identifying haplotype blocks |
gpls | Bioconductor Package Maintainer | Classification using generalized partial least squares |
gprege | Alfredo Kalaitzis | Gaussian Process Ranking and Estimation of Gene Expression time-series |
gpuMagic | Jiefei Wang | An openCL compiler with the capacity to compile R functions and run the code on GPU |
gQTLBase | VJ Carey | gQTLBase: infrastructure for eQTL, mQTL and similar studies |
gQTLstats | VJ Carey | gQTLstats: computationally efficient analysis for eQTL and allied studies |
gramm4R | Tianlu Chen | Generalized correlation analysis and model construction strategy for metabolome and microbiome |
graper | Britta Velten | Adaptive penalization in high-dimensional regression and classification with external covariates using variational Bayes |
graph | Bioconductor Package Maintainer | graph: A package to handle graph data structures |
GraphAlignment | Joern P. Meier | GraphAlignment |
GraphAT | Thomas LaFramboise | Graph Theoretic Association Tests |
graphite | Gabriele Sales | GRAPH Interaction from pathway Topological Environment |
GraphPAC | Gregory Ryslik | Identification of Mutational Clusters in Proteins via a Graph Theoretical Approach. |
GRENITS | Edward Morrissey | Gene Regulatory Network Inference Using Time Series |
GreyListChIP | Gordon Brown | Grey Lists -- Mask Artefact Regions Based on ChIP Inputs |
GRmetrics | Nicholas Clark, Mario Medvedovic | Calculate growth-rate inhibition (GR) metrics |
groHMM | Anusha Nagari, Tulip Nandu, W. Lee Kraus | GRO-seq Analysis Pipeline |
GRridge | Mark A. van de Wiel | Better prediction by use of co-data: Adaptive group-regularized ridge regression |
GSALightning | Billy Heung Wing Chang | Fast Permutation-based Gene Set Analysis |
GSAR | Yasir Rahmatallah, Galina Glazko | Gene Set Analysis in R |
GSCA | Zhicheng Ji | GSCA: Gene Set Context Analysis |
gscreend | Katharina Imkeller | Analysis of pooled genetic screens |
GSEABase | Bioconductor Package Maintainer | Gene set enrichment data structures and methods |
GSEABenchmarkeR | Ludwig Geistlinger | Reproducible GSEA Benchmarking |
GSEAlm | Assaf Oron | Linear Model Toolset for Gene Set Enrichment Analysis |
gsean | Dongmin Jung | Gene Set Enrichment Analysis with Networks |
GSReg | Bahman Afsari, Elana J. Fertig | Gene Set Regulation (GS-Reg) |
GSRI | Julian Gehring | Gene Set Regulation Index |
GSVA | Justin Guinney | Gene Set Variation Analysis for microarray and RNA-seq data |
gtrellis | Zuguang Gu | Genome Level Trellis Layout |
GUIDEseq | Lihua Julie Zhu | GUIDE-seq analysis pipeline |
Guitar | Jia Meng | Guitar |
Gviz | Robert Ivanek | Plotting data and annotation information along genomic coordinates |
gwascat | VJ Carey | representing and modeling data in the EMBL-EBI GWAS catalog |
GWASTools | Stephanie M. Gogarten | Tools for Genome Wide Association Studies |
gwasurvivr | Abbas Rizvi | gwasurvivr: an R package for genome wide survival analysis |
h5vc | Paul Theodor Pyl | Managing alignment tallies using a hdf5 backend |
hapFabia | Andreas Mitterecker | hapFabia: Identification of very short segments of identity by descent (IBD) characterized by rare variants in large sequencing data |
Harman | Jason Ross | The removal of batch effects from datasets using a PCA and constrained optimisation based technique |
Harshlight | Maurizio Pellegrino | A "corrective make-up" program for microarray chips |
HCABrowser | Bioconductor Package Maintainer | Browse the Human Cell Atlas data portal |
HCAExplorer | Bioconductor Package Maintainer | Browse the Human Cell Atlas data portal |
HDF5Array | Hervé Pagès | HDF5 backend for DelayedArray objects |
HDTD | Anestis Touloumis | Statistical Inference about the Mean Matrix and the Covariance Matrices in High-Dimensional Transposable Data (HDTD) |
heatmaps | Malcolm Perry | Flexible Heatmaps for Functional Genomics and Sequence Features |
Heatplus | Alexander Ploner | Heatmaps with row and/or column covariates and colored clusters |
HelloRanges | Michael Lawrence | Introduce *Ranges to bedtools users |
HELP | Reid F. Thompson | Tools for HELP data analysis |
HEM | HyungJun Cho | Heterogeneous error model for identification of differentially expressed genes under multiple conditions |
hiAnnotator | Nirav V Malani | Functions for annotating GRanges objects |
HIBAG | Xiuwen Zheng | HLA Genotype Imputation with Attribute Bagging |
HiCBricks | Koustav Pal | Framework for Storing and Accessing Hi-C Data Through HDF Files |
HiCcompare | John Stansfield | HiCcompare: Joint normalization and comparative analysis of multiple Hi-C datasets |
hicrep | Tao Yang | Measuring the reproducibility of Hi-C data |
hierGWAS | Laura Buzdugan | Asessing statistical significance in predictive GWA studies |
hierinf | Claude Renaux | Hierarchical Inference |
HilbertCurve | Zuguang Gu | Making 2D Hilbert Curve |
HilbertVis | Simon Anders | Hilbert curve visualization |
HilbertVisGUI | Simon Anders | HilbertVisGUI |
HiLDA | Zhi Yang | Conducting statistical inference on comparing the mutational exposures of mutational signatures by using hierarchical latent Dirichlet allocation |
hipathia | Marta R. Hidalgo | HiPathia: High-throughput Pathway Analysis |
HIPPO | Tae Kim | Heterogeneity-Induced Pre-Processing tOol |
hiReadsProcessor | Nirav V Malani | Functions to process LM-PCR reads from 454/Illumina data |
HIREewas | Xiangyu Luo | Detection of cell-type-specific risk-CpG sites in epigenome-wide association studies |
HiTC | Nicolas Servant | High Throughput Chromosome Conformation Capture analysis |
hmdbQuery | VJ Carey | utilities for exploration of human metabolome database |
HMMcopy | Daniel Lai, Sohrab Shah | Copy number prediction with correction for GC and mappability bias for HTS data |
hopach | Katherine S. Pollard | Hierarchical Ordered Partitioning and Collapsing Hybrid (HOPACH) |
HPAanalyze | Anh Nhat Tran | Retrieve and analyze data from the Human Protein Atlas |
hpar | Laurent Gatto | Human Protein Atlas in R |
HTqPCR | Heidi Dvinge | Automated analysis of high-throughput qPCR data |
HTSeqGenie | Jens Reeder | A NGS analysis pipeline. |
HTSFilter | Andrea Rau | Filter replicated high-throughput transcriptome sequencing data |
HumanTranscriptomeCompendium | VJ Carey | Tools to work with a Compendium of 181000 human transcriptome sequencing studies |
HybridMTest | Demba Fofana | Hybrid Multiple Testing |
hypeR | Anthony Federico | Hyper Enrichment |
hyperdraw | Paul Murrell | Visualizing Hypergaphs |
hypergraph | Bioconductor Package Maintainer | A package providing hypergraph data structures |
iASeq | Yingying Wei | iASeq: integrating multiple sequencing datasets for detecting allele-specific events |
iasva | Donghyung Lee, Anthony Cheng | Iteratively Adjusted Surrogate Variable Analysis |
iBBiG | Aedin Culhane | Iterative Binary Biclustering of Genesets |
ibh | Kircicegi Korkmaz | Interaction Based Homogeneity for Evaluating Gene Lists |
iBMQ | Greg Imholte | integrated Bayesian Modeling of eQTL data |
iCARE | Bill Wheeler | A Tool for Individualized Coherent Absolute Risk Estimation (iCARE) |
Icens | Bioconductor Package Maintainer | NPMLE for Censored and Truncated Data |
icetea | Vivek Bhardwaj | Integrating Cap Enrichment with Transcript Expression Analysis |
iCheck | Weiliang Qiu | QC Pipeline and Data Analysis Tools for High-Dimensional Illumina mRNA Expression Data |
iChip | Qianxing Mo | Bayesian Modeling of ChIP-chip Data Through Hidden Ising Models |
iClusterPlus | Qianxing Mo, Ronglai Shen | Integrative clustering of multi-type genomic data |
iCNV | Zilu Zhou | Integrated Copy Number Variation detection |
iCOBRA | Charlotte Soneson | Comparison and Visualization of Ranking and Assignment Methods |
ideal | Federico Marini | Interactive Differential Expression AnaLysis |
IdeoViz | Shraddha Pai | Plots data (continuous/discrete) along chromosomal ideogram |
idiogram | Karl J. Dykema | idiogram |
IdMappingAnalysis | Alex Lisovich, Roger Day | ID Mapping Analysis |
IdMappingRetrieval | Alex Lisovich, Roger Day | ID Mapping Data Retrieval |
idr2d | Konstantin Krismer | Irreproducible Discovery Rate for Genomic Interactions Data |
iGC | Liang-Bo Wang | An integrated analysis package of Gene expression and Copy number alteration |
IgGeneUsage | Simo Kitanovski | Differential gene usage in immune repertoires |
igvR | Paul Shannon | igvR: integrative genomics viewer |
IHW | Nikos Ignatiadis | Independent Hypothesis Weighting |
illuminaio | Kasper Daniel Hansen | Parsing Illumina Microarray Output Files |
imageHTS | Joseph Barry | Analysis of high-throughput microscopy-based screens |
IMAS | Seonggyun Han | Integrative analysis of Multi-omics data for Alternative Splicing |
Imetagene | Audrey Lemacon | A graphical interface for the metagene package |
IMMAN | Minoo Ashtiani | Interlog protein network reconstruction by Mapping and Mining ANalysis |
ImmuneSpaceR | ImmuneSpace Package Maintainer | A Thin Wrapper around the ImmuneSpace Database |
immunoClust | Till Soerensen | immunoClust - Automated Pipeline for Population Detection in Flow Cytometry |
IMPCdata | Jeremy Mason | Retrieves data from IMPC database |
ImpulseDE | Jil Sander, Nir Yosef | Detection of DE genes in time series data using impulse models |
ImpulseDE2 | David S Fischer | Differential expression analysis of longitudinal count data sets |
impute | Balasubramanian Narasimhan | impute: Imputation for microarray data |
INDEED | Ressom group, Yiming Zuo | Interactive Visualization of Integrated Differential Expression and Differential Network Analysis for Biomarker Candidate Selection Package |
infercnv | Christophe Georgescu | Infer Copy Number Variation from Single-Cell RNA-Seq Data |
InPAS | Jianhong Ou, Lihua Julie Zhu | InPAS: a bioconductor package for the identification of novel alternative PolyAdenylation Sites (PAS) using RNA-seq data |
INPower | Bill Wheeler | An R package for computing the number of susceptibility SNPs |
INSPEcT | Stefano de Pretis, Mattia Furlan | Modeling RNA synthesis, processing and degradation with RNA-seq data |
InTAD | Konstantin Okonechnikov | Search for correlation between epigenetic signals and gene expression in TADs |
intansv | Wen Yao | Integrative analysis of structural variations |
InteractionSet | Aaron Lun | Base Classes for Storing Genomic Interaction Data |
interactiveDisplay | Shawn Balcome | Package for enabling powerful shiny web displays of Bioconductor objects |
interactiveDisplayBase | Shawn Balcome | Base package for enabling powerful shiny web displays of Bioconductor objects |
IntEREst | Ali Oghabian, Mikko Frilander | Intron-Exon Retention Estimator |
InterMineR | InterMine Team | R Interface with InterMine-Powered Databases |
IntramiRExploreR | Surajit Bhattacharya | Predicting Targets for Drosophila Intragenic miRNAs |
inveRsion | Alejandro Caceres | Inversions in genotype data |
IONiseR | Mike Smith | Quality Assessment Tools for Oxford Nanopore MinION data |
iPAC | Gregory Ryslik | Identification of Protein Amino acid Clustering |
ipdDb | Steffen Klasberg | IPD IMGT/HLA and IPD KIR database for Homo sapiens |
IPO | Thomas Riebenbauer | Automated Optimization of XCMS Data Processing parameters |
IPPD | Martin Slawski | Isotopic peak pattern deconvolution for Protein Mass Spectrometry by template matching |
IRanges | Bioconductor Package Maintainer | Foundation of integer range manipulation in Bioconductor |
iSEE | Charlotte Soneson | Interactive SummarizedExperiment Explorer |
iSEEu | Kevin Rue-Albrecht | iSEE Universe |
iSeq | Qianxing Mo | Bayesian Hierarchical Modeling of ChIP-seq Data Through Hidden Ising Models |
isobar | Florian P Breitwieser | Analysis and quantitation of isobarically tagged MSMS proteomics data |
IsoCorrectoR | Christian Kohler | Correction for natural isotope abundance and tracer purity in MS and MS/MS data from stable isotope labeling experiments |
IsoCorrectoRGUI | Christian Kohler | Graphical User Interface for IsoCorrectoR |
IsoformSwitchAnalyzeR | Kristoffer Vitting-Seerup | Identify, Annotate and Visualize Alternative Splicing and Isoform Switches with Functional Consequences from both short- and long-read RNA-seq data. |
IsoGeneGUI | Setia Pramana | A graphical user interface to conduct a dose-response analysis of microarray data |
ISoLDE | Christelle Reynès | Integrative Statistics of alleLe Dependent Expression |
isomiRs | Lorena Pantano | Analyze isomiRs and miRNAs from small RNA-seq |
ITALICS | Guillem Rigaill | ITALICS |
iterativeBMA | Ka Yee Yeung | The Iterative Bayesian Model Averaging (BMA) algorithm |
iterativeBMAsurv | Ka Yee Yeung | The Iterative Bayesian Model Averaging (BMA) Algorithm For Survival Analysis |
iterClust | Hongxu Ding | Iterative Clustering |
iteremoval | Jiacheng Chuan | Iteration removal method for feature selection |
IVAS | Seonggyun Han | Identification of genetic Variants affecting Alternative Splicing |
ivygapSE | VJ Carey | A SummarizedExperiment for Ivy-GAP data |
IWTomics | Marzia A Cremona | Interval-Wise Testing for Omics Data |
joda | Ewa Szczurek | JODA algorithm for quantifying gene deregulation using knowledge |
JunctionSeq | Stephen Hartley | JunctionSeq: A Utility for Detection of Differential Exon and Splice-Junction Usage in RNA-Seq data |
karyoploteR | Bernat Gel | Plot customizable linear genomes displaying arbitrary data |
KCsmart | Jorma de Ronde | Multi sample aCGH analysis package using kernel convolution |
kebabs | Ulrich Bodenhofer | Kernel-Based Analysis Of Biological Sequences |
KEGGgraph | Jitao David Zhang | KEGGgraph: A graph approach to KEGG PATHWAY in R and Bioconductor |
KEGGlincs | Shana White, Mario Medvedovic | Visualize all edges within a KEGG pathway and overlay LINCS data |
keggorthology | VJ Carey | graph support for KO, KEGG Orthology |
KEGGprofile | Shilin Zhao | An annotation and visualization package for multi-types and multi-groups expression data in KEGG pathway |
KEGGREST | Bioconductor Package Maintainer | Client-side REST access to KEGG |
kimod | M L Zingaretti | A k-tables approach to integrate multiple Omics-Data |
KinSwingR | Ashley J. Waardenberg | KinSwingR: network-based kinase activity prediction |
kissDE | Aurélie Siberchicot | Retrieves Condition-Specific Variants in RNA-Seq Data |
KnowSeq | Daniel Castillo-Secilla | KnowSeq R/Bioc package: Beyond the traditional Transcriptomic pipeline |
LACE | Davide Maspero | Longitudinal Analysis of Cancer Evolution (LACE) |
lapmix | Yann Ruffieux | Laplace Mixture Model in Microarray Experiments |
LBE | Cyril Dalmasso | Estimation of the false discovery rate. |
ldblock | VJ Carey | data structures for linkage disequilibrium measures in populations |
LEA | Olivier Francois, Eric Frichot | LEA: an R package for Landscape and Ecological Association Studies |
LedPred | Aitor Gonzalez | Learning from DNA to Predict Enhancers |
les | Julian Gehring | Identifying Differential Effects in Tiling Microarray Data |
levi | Jose Luiz Rybarczyk Filho | Landscape Expression Visualization Interface |
lfa | Wei Hao, John D. Storey | Logistic Factor Analysis for Categorical Data |
limma | Gordon Smyth | Linear Models for Microarray Data |
limmaGUI | Gordon Smyth | GUI for limma Package With Two Color Microarrays |
LINC | Manuel Goepferich | co-expression of lincRNAs and protein-coding genes |
LineagePulse | David S Fischer | Differential expression analysis and model fitting for single-cell RNA-seq data |
LinkHD | "Laura M Zingaretti" | LinkHD: a versatile framework to explore and integrate heterogeneous data |
Linnorm | Ken Shun Hang Yip | Linear model and normality based normalization and transformation method (Linnorm) |
lionessR | Ping-Han Hsieh | Modeling networks for individual samples using LIONESS |
lipidr | Ahmed Mohamed | Data Mining and Analysis of Lipidomics Datasets |
LiquidAssociation | Yen-Yi Ho | LiquidAssociation |
lmdme | Cristobal Fresno | Linear Model decomposition for Designed Multivariate Experiments |
LMGene | Blythe Durbin-Johnson | LMGene Software for Data Transformation and Identification of Differentially Expressed Genes in Gene Expression Arrays |
LOBSTAHS | James Collins | Lipid and Oxylipin Biomarker Screening through Adduct Hierarchy Sequences |
loci2path | Tianlei Xu | Loci2path: regulatory annotation of genomic intervals based on tissue-specific expression QTLs |
logicFS | Holger Schwender | Identification of SNP Interactions |
logitT | Tobias Guennel | logit-t Package |
Logolas | Kushal Dey | EDLogo Plots Featuring String Logos and Adaptive Scaling of Position-Weight Matrices |
lol | Yinyin Yuan | Lots Of Lasso |
LOLA | Nathan Sheffield | Locus overlap analysis for enrichment of genomic ranges |
LoomExperiment | Bioconductor Package Maintainer | LoomExperiment container |
LowMACA | Stefano de Pretis, Giorgio Melloni | LowMACA - Low frequency Mutation Analysis via Consensus Alignment |
LPE | Nitin Jain | Methods for analyzing microarray data using Local Pooled Error (LPE) method |
LPEadj | Carl Murie | A correction of the local pooled error (LPE) method to replace the asymptotic variance adjustment with an unbiased adjustment based on sample size. |
lpNet | Lars Kaderali | Linear Programming Model for Network Inference |
lpsymphony | Vladislav Kim | Symphony integer linear programming solver in R |
LRBaseDbi | Koki Tsuyuzaki | DBI to construct LRBase-related package |
lumi | Lei Huang | BeadArray Specific Methods for Illumina Methylation and Expression Microarrays |
LVSmiRNA | Stefano Calza | LVS normalization for Agilent miRNA data |
LymphoSeq | David Coffey | Analyze high-throughput sequencing of T and B cell receptors |
M3C | Christopher John | Monte Carlo Reference-based Consensus Clustering |
M3D | Tom Mayo | Identifies differentially methylated regions across testing groups |
M3Drop | Tallulah Andrews | Michaelis-Menten Modelling of Dropouts in single-cell RNASeq |
maanova | Keith Sheppard | Tools for analyzing Micro Array experiments |
Maaslin2 | Lauren McIver | Maaslin2 |
macat | Joern Toedling | MicroArray Chromosome Analysis Tool |
maCorrPlot | Alexander Ploner | Visualize artificial correlation in microarray data |
MACPET | Ioannis Vardaxis | Model based analysis for paired-end data |
MACSQuantifyR | Raphaël Bonnet | Fast treatment of MACSQuantify FACS data |
made4 | Aedin Culhane | Multivariate analysis of microarray data using ADE4 |
MADSEQ | Yu Kong | Mosaic Aneuploidy Detection and Quantification using Massive Parallel Sequencing Data |
maftools | Anand Mayakonda | Summarize, Analyze and Visualize MAF Files |
MAGeCKFlute | Wubing Zhang | Integrative Analysis Pipeline for Pooled CRISPR Functional Genetic Screens |
maigesPack | Gustavo H. Esteves | Functions to handle cDNA microarray data, including several methods of data analysis |
MAIT | Pol Sola-Santos | Statistical Analysis of Metabolomic Data |
makecdfenv | James W. MacDonald | CDF Environment Maker |
MANOR | Pierre Neuvial | CGH Micro-Array NORmalization |
manta | Chris Berthiaume, Adrian Marchetti | Microbial Assemblage Normalized Transcript Analysis |
MantelCorr | Brian Steinmeyer | Compute Mantel Cluster Correlations |
mAPKL | Argiris Sakellariou | A Hybrid Feature Selection method for gene expression data |
maPredictDSC | Adi Laurentiu Tarca | Phenotype prediction using microarray data: approach of the best overall team in the IMPROVER Diagnostic Signature Challenge |
mapscape | Maia Smith | mapscape |
marray | Yee Hwa (Jean) Yang | Exploratory analysis for two-color spotted microarray data |
martini | Hector Climente-Gonzalez | GWAS Incorporating Networks |
maser | Diogo F.T. Veiga | Mapping Alternative Splicing Events to pRoteins |
maSigPro | Maria Jose Nueda | Significant Gene Expression Profile Differences in Time Course Gene Expression Data |
maskBAD | Michael Dannemann | Masking probes with binding affinity differences |
MassArray | Reid F. Thompson | Analytical Tools for MassArray Data |
massiR | Sam Buckberry | massiR: MicroArray Sample Sex Identifier |
MassSpecWavelet | Pan Du | Mass spectrum processing by wavelet-based algorithms |
MAST | Andrew McDavid | Model-based Analysis of Single Cell Transcriptomics |
matchBox | Luigi Marchionni, Anuj Gupta | Utilities to compute, compare, and plot the agreement between ordered vectors of features (ie. distinct genomic experiments). The package includes Correspondence-At-the-TOP (CAT) analysis. |
MatrixGenerics | Peter Hickey | S4 Generic Summary Statistic Functions that Operate on Matrix-Like Objects |
MatrixRider | Elena Grassi | Obtain total affinity and occupancies for binding site matrices on a given sequence |
matter | Kylie A. Bemis | A framework for rapid prototyping with file-based data structures |
MaxContrastProjection | Jan Sauer | Perform a maximum contrast projection of 3D images along the z-dimension into 2D |
MBAmethyl | Tao Wang | Model-based analysis of DNA methylation data |
MBASED | Oleg Mayba | Package containing functions for ASE analysis using Meta-analysis Based Allele-Specific Expression Detection |
MBCB | Jeff Allen | MBCB (Model-based Background Correction for Beadarray) |
mbkmeans | Davide Risso | Mini-batch K-means Clustering for Single-Cell RNA-seq |
mBPCR | P.M.V. Rancoita | Bayesian Piecewise Constant Regression for DNA copy number estimation |
MBQN | Ariane Schad | Mean/Median-balanced quantile normalization |
MBttest | Yuan-De Tan | Multiple Beta t-Tests |
mcaGUI | Wade K. Copeland | Microbial Community Analysis GUI |
MCbiclust | Robert Bentham | Massive correlating biclusters for gene expression data and associated methods |
MCRestimate | Marc Johannes | Misclassification error estimation with cross-validation |
mCSEA | Jordi Martorell-Marugán | Methylated CpGs Set Enrichment Analysis |
mdgsa | David Montaner | Multi Dimensional Gene Set Analysis. |
mdp | Helder Nakaya | Molecular Degree of Perturbation calculates scores for transcriptome data samples based on their perturbation from controls |
mdqc | Gabriela Cohen-Freue | Mahalanobis Distance Quality Control for microarrays |
MDTS | Jack M.. Fu | Detection of de novo deletion in targeted sequencing trios |
MEAL | Carlos Ruiz-Arenas | Perform methylation analysis |
MeasurementError.cor | Beiying Ding | Measurement Error model estimate for correlation coefficient |
MEAT | Sarah Voisin | Muscle Epigenetic Age Test |
MEB | Jiadi Zhu, Yan Zhou | A normalization-invariant minimum enclosing ball method to detect differentially expressed genes for RNA-seq data |
MEDIPS | Lukas Chavez | DNA IP-seq data analysis |
MEDME | Mattia Pelizzola | Modelling Experimental Data from MeDIP Enrichment |
MEIGOR | Jose A. Egea | MEIGO - MEtaheuristics for bIoinformatics Global Optimization |
Melissa | C. A. Kapourani | Bayesian clustering and imputationa of single cell methylomes |
MergeMaid | Xiaogang Zhong | Merge Maid |
Mergeomics | Zeyneb Kurt | Integrative network analysis of omics data |
MeSHDbi | Koki Tsuyuzaki | DBI to construct MeSH-related package from sqlite file |
meshes | Guangchuang Yu | MeSH Enrichment and Semantic analyses |
meshr | Koki Tsuyuzaki | Tools for conducting enrichment analysis of MeSH |
messina | Mark Pinese | Single-gene classifiers and outlier-resistant detection of differential expression for two-group and survival problems |
metaArray | Hyungwon Choi | Integration of Microarray Data for Meta-analysis |
Metab | Raphael Aggio | Metab: An R Package for a High-Throughput Analysis of Metabolomics Data Generated by GC-MS. |
metabomxtr | Michael Nodzenski | A package to run mixture models for truncated metabolomics data with normal or lognormal distributions |
MetaboSignal | Andrea Rodriguez-Martinez, Rafael Ayala | MetaboSignal: a network-based approach to overlay and explore metabolic and signaling KEGG pathways |
metaCCA | Anna Cichonska | Summary Statistics-Based Multivariate Meta-Analysis of Genome-Wide Association Studies Using Canonical Correlation Analysis |
MetaCyto | Zicheng Hu | MetaCyto: A package for meta-analysis of cytometry data |
metagene | Charles Joly Beauparlant | A package to produce metagene plots |
metagene2 | Eric Fournier | A package to produce metagene plots |
metagenomeFeatures | Nathan D. Olson | Exploration of marker-gene sequence taxonomic annotations |
metagenomeSeq | Joseph N. Paulson | Statistical analysis for sparse high-throughput sequencing |
metahdep | John R. Stevens | Hierarchical Dependence in Meta-Analysis |
metaMS | Yann Guitton | MS-based metabolomics annotation pipeline |
MetaNeighbor | Manthan Shah | Single cell replicability analysis |
metaSeq | Koki Tsuyuzaki | Meta-analysis of RNA-Seq count data in multiple studies |
metaseqR | Panagiotis Moulos | An R package for the analysis and result reporting of RNA-Seq data by combining multiple statistical algorithms. |
metaseqR2 | Panagiotis Moulos | An R package for the analysis and result reporting of RNA-Seq data by combining multiple statistical algorithms |
metavizr | Hector Corrada Bravo | R Interface to the metaviz web app for interactive metagenomics data analysis and visualization |
MetaVolcanoR | Cesar Prada | Gene Expression Meta-analysis Visualization Tool |
MetCirc | Thomas Naake | Navigating mass spectral similarity in high-resolution MS/MS metabolomics data |
MethCP | Boying Gong | Differential methylation anlsysis for bisulfite sequencing data |
methimpute | Aaron Taudt | Imputation-guided re-construction of complete methylomes from WGBS data |
methInheritSim | Pascal Belleau | Simulating Whole-Genome Inherited Bisulphite Sequencing Data |
MethPed | Helena Carén | A DNA methylation classifier tool for the identification of pediatric brain tumor subtypes |
methrix | Anand Mayakonda | Fast and efficient summarization of generic bedGraph files from Bisufite sequencing |
MethTargetedNGS | Muhammad Ahmer Jamil | Perform Methylation Analysis on Next Generation Sequencing Data |
methVisual | Arie Zackay | Methods for visualization and statistics on DNA methylation data |
methyAnalysis | Lei Huang | DNA methylation data analysis and visualization |
MethylAid | L.J.Sinke | Visual and interactive quality control of large Illumina DNA Methylation array data sets |
methylCC | Stephanie C. Hicks | Estimate the cell composition of whole blood in DNA methylation samples |
methylGSA | Xu Ren | Gene Set Analysis Using the Outcome of Differential Methylation |
methylInheritance | Astrid Deschenes | Permutation-Based Analysis associating Conserved Differentially Methylated Elements Across Multiple Generations to a Treatment Effect |
methylKit | Altuna Akalin, Alexander Gosdschan | DNA methylation analysis from high-throughput bisulfite sequencing results |
MethylMix | Olivier Gevaert | MethylMix: Identifying methylation driven cancer genes |
methylMnM | Yan Zhou | detect different methylation level (DMR) |
methylPipe | Kamal Kishore | Base resolution DNA methylation data analysis |
MethylSeekR | Lukas Burger | Segmentation of Bis-seq data |
methylSig | Raymond G. Cavalcante | MethylSig: Differential Methylation Testing for WGBS and RRBS Data |
methylumi | Sean Davis | Handle Illumina methylation data |
methyvim | Nima Hejazi | Targeted, Robust, and Model-free Differential Methylation Analysis |
MetID | Zhenzhi Li | Network-based prioritization of putative metabolite IDs |
MetNet | Thomas Naake | Inferring metabolic networks from untargeted high-resolution mass spectrometry data |
mfa | Kieran Campbell | Bayesian hierarchical mixture of factor analyzers for modelling genomic bifurcations |
Mfuzz | Matthias Futschik | Soft clustering of time series gene expression data |
MGFM | Khadija El Amrani | Marker Gene Finder in Microarray gene expression data |
MGFR | Khadija El Amrani | Marker Gene Finder in RNA-seq data |
mgsa | Sebastian Bauer | Model-based gene set analysis |
MiChip | Jonathon Blake | MiChip Parsing and Summarizing Functions |
microbiome | Leo Lahti | Microbiome Analytics |
microbiomeDASim | Justin Williams | Microbiome Differential Abundance Simulation |
MicrobiotaProcess | Shuangbin Xu | an R package for analysis, visualization and biomarker discovery of microbiome |
microRNA | "James F. Reid" | Data and functions for dealing with microRNAs |
MIGSA | Juan C. Rodriguez | Massive and Integrative Gene Set Analysis |
mimager | Aaron Wolen | mimager: The Microarray Imager |
MIMOSA | Greg Finak | Mixture Models for Single-Cell Assays |
MineICA | Anne Biton | Analysis of an ICA decomposition obtained on genomics data |
minet | Patrick E. Meyer | Mutual Information NETworks |
minfi | Kasper Daniel Hansen | Analyze Illumina Infinium DNA methylation arrays |
MinimumDistance | Robert B Scharpf | A Package for De Novo CNV Detection in Case-Parent Trios |
MiPP | Sukwoo Kim | Misclassification Penalized Posterior Classification |
MIRA | John Lawson | Methylation-Based Inference of Regulatory Activity |
MiRaGE | Y-h. Taguchi | MiRNA Ranking by Gene Expression |
miRBaseConverter | Taosheng Xu | A comprehensive and high-efficiency tool for converting and retrieving the information of miRNAs in different miRBase versions |
miRcomp | Matthew N. McCall | Tools to assess and compare miRNA expression estimatation methods |
mirIntegrator | Diana Diaz | Integrating microRNA expression into signaling pathways for pathway analysis |
miRLAB | Thuc Duy Le | Dry lab for exploring miRNA-mRNA relationships |
miRmine | Dusan Randjelovic | Data package with miRNA-seq datasets from miRmine database as RangedSummarizedExperiment |
miRNAmeConverter | Stefan J. Haunsberger | Convert miRNA Names to Different miRBase Versions |
miRNApath | James M. Ward | miRNApath: Pathway Enrichment for miRNA Expression Data |
miRNAtap | T. Ian Simpson | miRNAtap: microRNA Targets - Aggregated Predictions |
miRSM | Junpeng Zhang | Inferring miRNA sponge modules by integrating expression data and miRNA-target binding information |
miRspongeR | Junpeng Zhang | Identification and analysis of miRNA sponge interaction networks and modules |
Mirsynergy | Yue Li | Mirsynergy |
missMethyl | Belinda Phipson, Jovana Maksimovic, Andrew Lonsdale | Analysing Illumina HumanMethylation BeadChip Data |
missRows | Gonzalez Ignacio | Handling Missing Individuals in Multi-Omics Data Integration |
mitch | Mark Ziemann | Multi-Contrast Gene Set Enrichment Analysis |
mitoODE | Gregoire Pau | Implementation of the differential equation model described in "Dynamical modelling of phenotypes in a genome-wide RNAi live-cell imaging assay" |
mixOmics | Kim-Anh Le Cao | Omics Data Integration Project |
MLInterfaces | V. Carey | Uniform interfaces to R machine learning procedures for data in Bioconductor containers |
MLP | Tobias Verbeke | MLP |
MLSeq | Gokmen Zararsiz | Machine Learning Interface for RNA-Seq Data |
MMAPPR2 | Jonathon Hill | Mutation Mapping Analysis Pipeline for Pooled RNA-Seq |
MMDiff2 | Gabriele Schweikert | Statistical Testing for ChIP-Seq data sets |
MmPalateMiRNA | Guy Brock | Murine Palate miRNA Expression Analysis |
MMUPHin | Siyuan MA | Meta-analysis Methods with Uniform Pipeline for Heterogeneity in Microbiome Studies |
mnem | Martin Pirkl | Mixture Nested Effects Models |
MODA | Dong Li | MODA: MOdule Differential Analysis for weighted gene co-expression network |
Modstrings | Felix G.M. Ernst | Working with modified nucleotide sequences |
MOFA | Britta Velten | Multi-Omics Factor Analysis (MOFA) |
mogsa | Chen Meng | Multiple omics data integrative clustering and gene set analysis |
MOMA | Sunny Jones | Multi Omic Master Regulator Analysis |
monocle | Cole Trapnell | Clustering, differential expression, and trajectory analysis for single- cell RNA-Seq |
MoonlightR | Antonio Colaprico, Catharina Olsen | Identify oncogenes and tumor suppressor genes from omics data |
MoPS | Philipp Eser | MoPS - Model-based Periodicity Screening |
mosaics | Dongjun Chung | MOSAiCS (MOdel-based one and two Sample Analysis and Inference for ChIP-Seq) |
MOSim | Carlos Martínez | Multi-Omics Simulation (MOSim) |
motifbreakR | Simon Gert Coetzee | A Package For Predicting The Disruptiveness Of Single Nucleotide Polymorphisms On Transcription Factor Binding Sites |
motifcounter | Wolfgang Kopp | R package for analysing TFBSs in DNA sequences |
MotifDb | Paul Shannon | An Annotated Collection of Protein-DNA Binding Sequence Motifs |
motifmatchr | Alicia Schep | Fast Motif Matching in R |
motifRG | Zizhen Yao | A package for discriminative motif discovery, designed for high throughput sequencing dataset |
motifStack | Jianhong Ou | Plot stacked logos for single or multiple DNA, RNA and amino acid sequence |
MotIV | Eloi Mercier, Raphael Gottardo | Motif Identification and Validation |
MPFE | Conrad Burden | Estimation of the amplicon methylation pattern distribution from bisulphite sequencing data |
mpra | Leslie Myint | Analyze massively parallel reporter assays |
MPRAnalyze | Tal Ashuach | Statistical Analysis of MPRA data |
msa | Ulrich Bodenhofer | Multiple Sequence Alignment |
MsCoreUtils | RforMassSpectrometry Package Maintainer | Core Utils for Mass Spectrometry Data |
msgbsR | Benjamin Mayne | msgbsR: methylation sensitive genotyping by sequencing (MS-GBS) R functions |
MSGFgui | Thomas Lin Pedersen | A shiny GUI for MSGFplus |
MSGFplus | Thomas Lin Pedersen | An interface between R and MS-GF+ |
msmsEDA | Josep Gregori | Exploratory Data Analysis of LC-MS/MS data by spectral counts |
msmsTests | Josep Gregori i Font | LC-MS/MS Differential Expression Tests |
MSnbase | Laurent Gatto | Base Functions and Classes for Mass Spectrometry and Proteomics |
MSnID | Vlad Petyuk | Utilities for Exploration and Assessment of Confidence of LC-MSn Proteomics Identifications |
msPurity | Thomas N. Lawson | Automated Evaluation of Precursor Ion Purity for Mass Spectrometry Based Fragmentation in Metabolomics |
MSstats | Meena Choi | Protein Significance Analysis in DDA, SRM and DIA for Label-free or Label-based Proteomics Experiments |
MSstatsQC | Eralp Dogu | Longitudinal system suitability monitoring and quality control for proteomic experiments |
MSstatsQCgui | Eralp Dogu | A graphical user interface for MSstatsQC package |
MSstatsSampleSize | Ting Huang | Simulation tool for optimal design of high-dimensional MS-based proteomics experiment |
MSstatsTMT | Ting Huang | Protein Significance Analysis in shotgun mass spectrometry-based proteomic experiments with tandem mass tag (TMT) labeling |
MTseeker | Tim Triche | Bioconductor Tools for Human Mitochondrial Variant Analysis |
Mulcom | Claudio Isella | Calculates Mulcom test |
MultiAssayExperiment | Marcel Ramos | Software for the integration of multi-omics experiments in Bioconductor |
multiClust | Nathan Lawlor | multiClust: An R-package for Identifying Biologically Relevant Clusters in Cancer Transcriptome Profiles |
MultiDataSet | Carlos Ruiz-Arenas | Implementation of MultiDataSet and ResultSet |
multiHiCcompare | John Stansfield | Normalize and detect differences between Hi-C datasets when replicates of each experimental condition are available |
MultiMed | Simina M. Boca | Testing multiple biological mediators simultaneously |
multiMiR | Matt Mulvahill | Integration of multiple microRNA-target databases with their disease and drug associations |
multiOmicsViz | Jing Wang | Plot the effect of one omics data on other omics data along the chromosome |
multiscan | Mizanur Khondoker | R package for combining multiple scans |
multtest | Katherine S. Pollard | Resampling-based multiple hypothesis testing |
muscat | Helena L. Crowell | Multi-sample multi-group scRNA-seq data analysis tools |
muscle | Alex T. Kalinka | Multiple Sequence Alignment with MUSCLE |
MutationalPatterns | Rurika Oka, Freek Manders | Comprehensive genome-wide analysis of mutational processes |
MVCClass | Elizabeth Whalen | Model-View-Controller (MVC) Classes |
MWASTools | Andrea Rodriguez-Martinez, Rafael Ayala | MWASTools: an integrated pipeline to perform metabolome-wide association studies |
mygene | Adam Mark, Cyrus Afrasiabi, Chunlei Wu | Access MyGene.Info_ services |
myvariant | Adam Mark, Chunlei Wu | Accesses MyVariant.info variant query and annotation services |
mzID | Laurent Gatto | An mzIdentML parser for R |
mzR | Steffen Neumann, Laurent Gatto, Qiang Kou | parser for netCDF, mzXML, mzData and mzML and mzIdentML files (mass spectrometry data) |
NADfinder | Jianhong Ou, Lihua Julie Zhu | Call wide peaks for sequencing data |
NanoStringDiff | tingting zhai,hong wang | Differential Expression Analysis of NanoString nCounter Data |
NanoStringQCPro | Robert Ziman | Quality metrics and data processing methods for NanoString mRNA gene expression data |
nanotatoR | Surajit Bhattacharya | nanotatoR: next generation structural variant annotation and classification |
NarrowPeaks | Pedro Madrigal | Shape-based Analysis of Variation in ChIP-seq using Functional PCA |
NBAMSeq | Xu Ren | Negative Binomial Additive Model for RNA-Seq Data |
NBSplice | Gabriela Merino | Negative Binomial Models to detect Differential Splicing |
ncdfFlow | Mike Jiang, Jake Wagner | ncdfFlow: A package that provides HDF5 based storage for flow cytometry data. |
ncGTW | Chiung-Ting Wu | Alignment of LC-MS Profiles by Neighbor-wise Compound-specific Graphical Time Warping with Misalignment Detection |
NCIgraph | Laurent Jacob | Pathways from the NCI Pathways Database |
ndexr | Florian Auer | NDEx R client library |
NeighborNet | Sahar Ansari | Neighbor_net analysis |
nem | Holger Froehlich | (Dynamic) Nested Effects Models and Deterministic Effects Propagation Networks to reconstruct phenotypic hierarchies |
netbenchmark | Pau Bellot | Benchmarking of several gene network inference methods |
netbiov | Shailesh tripathi | A package for visualizing complex biological network |
netboost | Pascal Schlosser | Network Analysis Supported by Boosting |
netboxr | Eirc Minwei Liu | netboxr |
netDx | Shraddha Pai | Network-based patient classifier |
nethet | Nicolas Staedler, Frank Dondelinger | A bioconductor package for high-dimensional exploration of biological network heterogeneity |
NetPathMiner | Ahmed Mohamed | NetPathMiner for Biological Network Construction, Path Mining and Visualization |
netprioR | Fabian Schmich | A model for network-based prioritisation of genes |
netReg | Simon Dirmeier | Network-Regularized Regression Models |
netresponse | Leo Lahti | Functional Network Analysis |
NetSAM | Bing Zhang | Network Seriation And Modularization |
netSmooth | Jonathan Ronen | Network smoothing for scRNAseq |
networkBMA | Ka Yee Yeung | Regression-based network inference using Bayesian Model Averaging |
ngsReports | Steve Pederson | Load FastqQC reports and other NGS related files |
nnNorm | Adi Laurentiu Tarca | Spatial and intensity based normalization of cDNA microarray data based on robust neural nets |
NOISeq | Sonia Tarazona | Exploratory analysis and differential expression for RNA-seq data |
nondetects | Valeriia Sherina | Non-detects in qPCR data |
NoRCE | Gulden Olgun | NoRCE: Noncoding RNA Sets Cis Annotation and Enrichment |
normalize450K | Jonathan Alexander Heiss | Preprocessing of Illumina Infinium 450K data |
NormalyzerDE | Jakob Willforss | Evaluation of normalization methods and calculation of differential expression analysis statistics |
NormqPCR | James Perkins | Functions for normalisation of RT-qPCR data |
normr | Johannes Helmuth | Normalization and difference calling in ChIP-seq data |
NPARC | Nils Kurzawa | Non-parametric analysis of response curves for thermal proteome profiling experiments |
npGSEA | Jessica Larson | Permutation approximation methods for gene set enrichment analysis (non-permutation GSEA) |
NTW | Yuanhua Liu | Predict gene network using an Ordinary Differential Equation (ODE) based method |
nucleoSim | Astrid Deschenes | Generate synthetic nucleosome maps |
nucleR | Diego Gallego | Nucleosome positioning package for R |
nuCpos | Hiroaki Kato | An R package for prediction of nucleosome positions |
NuPoP | Ji-Ping Wang | An R package for nucleosome positioning prediction |
occugene | Oliver Will | Functions for Multinomial Occupancy Distribution |
OCplus | Alexander Ploner | Operating characteristics plus sample size and local fdr for microarray experiments |
odseq | José Jiménez | Outlier detection in multiple sequence alignments |
OGSA | Michael F. Ochs | Outlier Gene Set Analysis |
oligo | Benilton Carvalho | Preprocessing tools for oligonucleotide arrays |
oligoClasses | Benilton Carvalho and Robert Scharpf | Classes for high-throughput arrays supported by oligo and crlmm |
OLIN | Matthias Futschik | Optimized local intensity-dependent normalisation of two-color microarrays |
OLINgui | Matthias Futschik | Graphical user interface for OLIN |
OmaDB | Klara Kaleb, Adrian Altenhoff | R wrapper for the OMA REST API |
omicade4 | Chen Meng | Multiple co-inertia analysis of omics datasets |
OmicCircos | Ying Hu | High-quality circular visualization of omics data |
omicplotR | Daniel Giguere | Visual Exploration of Omic Datasets Using a Shiny App |
omicRexposome | Carles Hernandez-Ferrer | Exposome and omic data associatin and integration analysis |
OmicsLonDA | Ahmed A. Metwally | Omics Longitudinal Differential Analysis |
OmicsMarkeR | Charles E. Determan Jr. | Classification and Feature Selection for 'Omics' Datasets |
OMICsPCA | Subhadeep Das | An R package for quantitative integration and analysis of multiple omics assays from heterogeneous samples |
omicsPrint | Davy Cats | Cross omic genetic fingerprinting |
OmnipathR | Alberto Valdeolivas Urbelz | Import Omnipath network |
Onassis | Eugenia Galeota | OnASSIs Ontology Annotation and Semantic SImilarity software |
oncomix | Daniel Pique | Identifying Genes Overexpressed in Subsets of Tumors from Tumor-Normal mRNA Expression Data |
OncoScore | Luca De Sano | A tool to identify potentially oncogenic genes |
OncoSimulR | Ramon Diaz-Uriarte | Forward Genetic Simulation of Cancer Progression with Epistasis |
oneSENSE | Yong Kee Tan | One-Dimensional Soli-Expression by Nonlinear Stochastic Embedding (OneSENSE) |
onlineFDR | David S. Robertson | Online error control |
ontoProc | VJ Carey | processing of ontologies of anatomy, cell lines, and so on |
openCyto | Mike Jiang,Jake Wagner | Hierarchical Gating Pipeline for flow cytometry data |
openPrimeR | Matthias Döring | Multiplex PCR Primer Design and Analysis |
openPrimeRui | Matthias Döring | Shiny Application for Multiplex PCR Primer Design and Analysis |
OpenStats | Hamed Haseli Mashhadi | A Robust and Scalable Software Package for Reproducible Analysis of High-Throughput genotype-phenotype association |
oposSOM | Henry Loeffler-Wirth | Comprehensive analysis of transciptome data |
oppar | Soroor Hediyeh zadeh | Outlier profile and pathway analysis in R |
oppti | Abdulkadir Elmas | Outlier Protein and Phosphosite Target Identifier |
optimalFlow | Hristo Inouzhe | optimalFlow |
OPWeight | Mohamad Hasan | Optimal p-value weighting with independent information |
OrderedList | Claudio Lottaz | Similarities of Ordered Gene Lists |
ORFik | Haakon Tjeldnes | Open Reading Frames in Genomics |
Organism.dplyr | Martin Morgan | dplyr-based Access to Bioconductor Annotation Resources |
OrganismDbi | Bioconductor Package Maintainer | Software to enable the smooth interfacing of different database packages |
OSAT | Li Yan | OSAT: Optimal Sample Assignment Tool |
Oscope | Ning Leng | Oscope - A statistical pipeline for identifying oscillatory genes in unsynchronized single cell RNA-seq |
OTUbase | Daniel Beck | Provides structure and functions for the analysis of OTU data |
OutlierD | Sukwoo Kim | Outlier detection using quantile regression on the M-A scatterplots of high-throughput data |
OUTRIDER | Christian Mertes | OUTRIDER - OUTlier in RNA-Seq fInDER |
OVESEG | Lulu Chen | OVESEG-test to detect tissue/cell-specific markers |
PAA | Michael Turewicz, Martin Eisenacher | PAA (Protein Array Analyzer) |
packFinder | Jack Gisby | de novo Annotation of Pack-TYPE Transposable Elements |
PADOG | Adi Laurentiu Tarca | Pathway Analysis with Down-weighting of Overlapping Genes (PADOG) |
PAIRADISE | Qiang Hu, Levon Demirdjian | PAIRADISE: Paired analysis of differential isoform expression |
paircompviz | Michal Burda | Multiple comparison test visualization |
pandaR | Joseph N. Paulson, Dan Schlauch | PANDA Algorithm |
panelcn.mops | Gundula Povysil | CNV detection tool for targeted NGS panel data |
panp | Peter Warren | Presence-Absence Calls from Negative Strand Matching Probesets |
PANR | Xin Wang | Posterior association networks and functional modules inferred from rich phenotypes of gene perturbations |
PanVizGenerator | Thomas Lin Pedersen | Generate PanViz visualisations from your pangenome |
PAPi | Raphael Aggio | Predict metabolic pathway activity based on metabolomics data |
parglms | VJ Carey | support for parallelized estimation of GLMs/GEEs |
parody | VJ Carey | Parametric And Resistant Outlier DYtection |
PAST | Thrash Adam | Pathway Association Study Tool (PAST) |
Path2PPI | Oliver Philipp | Prediction of pathway-related protein-protein interaction networks |
pathifier | Assif Yitzhaky | Quantify deregulation of pathways in cancer |
PathNet | Ludwig Geistlinger | An R package for pathway analysis using topological information |
PathoStat | Solaiappan Manimaran, Yue Zhao | PathoStat Statistical Microbiome Analysis Package |
pathprint | Sokratis Kariotis | Pathway fingerprinting for analysis of gene expression arrays |
pathRender | Vince Carey | Render molecular pathways |
pathVar | Samuel Zimmerman | Methods to Find Pathways with Significantly Different Variability |
pathview | Weijun Luo | a tool set for pathway based data integration and visualization |
pathwayPCA | Gabriel Odom | Integrative Pathway Analysis with Modern PCA Methodology and Gene Selection |
PathwaySplice | Aimin Yan | An R Package for Unbiased Splicing Pathway Analysis |
paxtoolsr | Augustin Luna | PaxtoolsR: Access Pathways from Multiple Databases through BioPAX and Pathway Commons |
pcaExplorer | Federico Marini | Interactive Visualization of RNA-seq Data Using a Principal Components Approach |
pcaGoPromoter | Morten Hansen | pcaGoPromoter is used to analyze DNA micro array data |
pcaMethods | Henning Redestig | A collection of PCA methods |
PCAN | Matthew Page and Patrice Godard | Phenotype Consensus ANalysis (PCAN) |
PCAtools | Kevin Blighe | PCAtools: Everything Principal Components Analysis |
pcot2 | Sarah Song | Principal Coordinates and Hotelling's T-Square method |
PCpheno | Nolwenn Le Meur | Phenotypes and cellular organizational units |
pcxn | Sokratis Kariotis | Exploring, analyzing and visualizing functions utilizing the pcxnData package |
pdInfoBuilder | Benilton Carvalho | Platform Design Information Package Builder |
peakPantheR | Arnaud Wolfer | Peak Picking and Annotation of High Resolution Experiments |
PECA | Tomi Suomi | Probe-level Expression Change Averaging |
peco | Chiaowen Joyce Hsiao | A Supervised Approach for **P**r**e**dicting **c**ell Cycle Pr**o**gression using scRNA-seq data |
PepsNMR | Manon Martin | Pre-process 1H-NMR FID signals |
pepStat | Gregory C Imholte | Statistical analysis of peptide microarrays |
pepXMLTab | Xiaojing Wang | Parsing pepXML files and filter based on peptide FDR. |
PERFect | Quy Cao | Permutation filtration for microbiome data |
perturbatr | Simon Dirmeier | Statistical Analysis of High-Throughput Genetic Perturbation Screens |
PGA | Bo Wen, Shaohang Xu | An package for identification of novel peptides by customized database derived from RNA-Seq |
pgca | Gabriela Cohen-Freue | PGCA: An Algorithm to Link Protein Groups Created from MS/MS Data |
PGSEA | Karl Dykema | Parametric Gene Set Enrichment Analysis |
phantasus | Alexey Sergushichev | Visual and interactive gene expression analysis |
PharmacoGx | Benjamin Haibe-Kains | Analysis of Large-Scale Pharmacogenomic Data |
phemd | William S Chen | Phenotypic EMD for comparison of single-cell samples |
phenopath | Kieran Campbell | Genomic trajectories with heterogeneous genetic and environmental backgrounds |
phenoTest | Evarist Planet | Tools to test association between gene expression and phenotype in a way that is efficient, structured, fast and scalable. We also provide tools to do GSEA (Gene set enrichment analysis) and copy number variation. |
PhenStat | Hamed Haselimashhadi | Statistical analysis of phenotypic data |
philr | Justin Silverman | Phylogenetic partitioning based ILR transform for metagenomics data |
phosphonormalizer | Sohrab Saraei | Compensates for the bias introduced by median normalization in phosphoproteomics |
PhyloProfile | Vinh Tran | PhyloProfile |
phyloseq | Paul J. McMurdie | Handling and analysis of high-throughput microbiome census data |
Pi | Hai Fang | Leveraging Genetic Evidence to Prioritise Drug Targets at the Gene and Pathway Level |
piano | Leif Varemo Wigge | Platform for integrative analysis of omics data |
pickgene | Brian S. Yandell | Adaptive Gene Picking for Microarray Expression Data Analysis |
PICS | Renan Sauteraud | Probabilistic inference of ChIP-seq |
Pigengene | Habil Zare | Infers biological signatures from gene expression data |
PING | Renan Sauteraud | Probabilistic inference for Nucleosome Positioning with MNase-based or Sonicated Short-read Data |
pint | Olli-Pekka Huovilainen | Pairwise INTegration of functional genomics data |
pipeFrame | Zheng Wei | Pipeline framework for bioinformatics in R |
pkgDepTools | Bioconductor Package Maintainer | Package Dependency Tools |
plethy | Daniel Bottomly | R framework for exploration and analysis of respirometry data |
plgem | Norman Pavelka | Detect differential expression in microarray and proteomics datasets with the Power Law Global Error Model (PLGEM) |
plier | Crispin Miller | Implements the Affymetrix PLIER algorithm |
PloGO2 | Jemma Wu, Dana Pascovici | Plot Gene Ontology and KEGG pathway Annotation and Abundance |
plotGrouper | John D. Gagnon | Shiny app GUI wrapper for ggplot with built-in statistical analysis |
PLPE | Soo-heang Eo | Local Pooled Error Test for Differential Expression with Paired High-throughput Data |
plrs | Gwenael G.R. Leday to | Piecewise Linear Regression Splines (PLRS) for the association between DNA copy number and gene expression |
plw | Magnus Astrand | Probe level Locally moderated Weighted t-tests. |
plyranges | Stuart Lee | A fluent interface for manipulating GenomicRanges |
pmm | Anna Drewek | Parallel Mixed Model |
pmp | Andris Jankevics | Peak Matrix Processing and signal batch correction for metabolomics datasets |
podkat | Ulrich Bodenhofer | Position-Dependent Kernel Association Test |
pogos | VJ Carey | PharmacOGenomics Ontology Support |
polyester | Jack Fu, Jeff Leek | Simulate RNA-seq reads |
Polyfit | Conrad Burden | Add-on to DESeq to improve p-values and q-values |
POST | Xueyuan Cao | Projection onto Orthogonal Space Testing for High Dimensional Data |
PoTRA | Valentin Dinu | PoTRA: Pathways of Topological Rank Analysis |
PowerExplorer | Xu Qiao | Power Estimation Tool for RNA-Seq and proteomics data |
powerTCR | Hillary Koch | Model-Based Comparative Analysis of the TCR Repertoire |
PPInfer | Dongmin Jung | Inferring functionally related proteins using protein interaction networks |
ppiStats | Bioconductor Package Maintainer | Protein-Protein Interaction Statistical Package |
pqsfinder | Jiri Hon | Identification of potential quadruplex forming sequences |
prada | Florian Hahne | Data analysis for cell-based functional assays |
pram | Peng Liu | Pooling RNA-seq datasets for assembling transcript models |
prebs | Karolis Uziela | Probe region expression estimation for RNA-seq data for improved microarray comparability |
PrecisionTrialDrawer | Giorgio Melloni | A Tool to Analyze and Design NGS Based Custom Gene Panels |
PREDA | Francesco Ferrari | Position Related Data Analysis |
predictionet | Benjamin Haibe-Kains, Catharina Olsen | Inference for predictive networks designed for (but not limited to) genomic data |
preprocessCore | Ben Bolstad | A collection of pre-processing functions |
primirTSS | Pumin Li | Prediction of pri-miRNA Transcription Start Site |
PrInCE | Michael Skinnider | Predicting Interactomes from Co-Elution |
Prize | Daryanaz Dargahi | Prize: an R package for prioritization estimation based on analytic hierarchy process |
proBAMr | Xiaojing Wang | Generating SAM file for PSMs in shotgun proteomics data |
proBatch | Chloe H. Lee | Tools for Diagnostics and Corrections of Batch Effects in Proteomics |
PROcess | Xiaochun Li | Ciphergen SELDI-TOF Processing |
procoil | Ulrich Bodenhofer | Prediction of Oligomerization of Coiled Coil Proteins |
proDA | Constantin Ahlmann-Eltze | Differential Abundance Analysis of Label-Free Mass Spectrometry Data |
proFIA | Alexis Delabriere | Preprocessing of FIA-HRMS data |
profileplyr | Tom Carroll, Doug Barrows | Visualization and annotation of read signal over genomic ranges with profileplyr |
profileScoreDist | Paal O. Westermark | Profile score distributions |
progeny | Alberto Valdeolivas | Pathway RespOnsive GENes for activity inference from gene expression |
projectR | Genevieve Stein-O'Brien | Functions for the projection of weights from PCA, CoGAPS, NMF, correlation, and clustering |
pRoloc | Laurent Gatto | A unifying bioinformatics framework for spatial proteomics |
pRolocGUI | Laurent Gatto | Interactive visualisation of spatial proteomics data |
PROMISE | Stan Pounds, Xueyuan Cao | PRojection Onto the Most Interesting Statistical Evidence |
PROPER | Hao Wu | PROspective Power Evaluation for RNAseq |
PROPS | Lichy Han | PRObabilistic Pathway Score (PROPS) |
Prostar | Samuel Wieczorek | Provides a GUI for DAPAR |
proteinProfiles | Julian Gehring | Protein Profiling |
ProteomicsAnnotationHubData | Laurent Gatto | Transform public proteomics data resources into Bioconductor Data Structures |
ProteoMM | Yuliya V Karpievitch | Multi-Dataset Model-based Differential Expression Proteomics Analysis Platform |
proteoQC | Bo Wen | An R package for proteomics data quality control |
ProtGenerics | Laurent Gatto | S4 generic functions for Bioconductor proteomics infrastructure |
PSEA | Alexandre Kuhn | Population-Specific Expression Analysis. |
psichomics | Nuno Saraiva-Agostinho | Graphical Interface for Alternative Splicing Quantification, Analysis and Visualisation |
PSICQUIC | Paul Shannon | Proteomics Standard Initiative Common QUery InterfaCe |
psygenet2r | Alba Gutierrez-Sacristan | psygenet2r - An R package for querying PsyGeNET and to perform comorbidity studies in psychiatric disorders |
PubScore | Tiago Lubiana | Automatic calculation of literature relevance of genes |
pulsedSilac | Marc Pagès-Gallego | Analysis of pulsed-SILAC quantitative proteomics data |
puma | Xuejun Liu | Propagating Uncertainty in Microarray Analysis(including Affymetrix tranditional 3' arrays and exon arrays and Human Transcriptome Array 2.0) |
PureCN | Markus Riester | Copy number calling and SNV classification using targeted short read sequencing |
pvac | Jun Lu, Pierre R. Bushel | PCA-based gene filtering for Affymetrix arrays |
pvca | Jianying LI | Principal Variance Component Analysis (PVCA) |
Pviz | Renan Sauteraud | Peptide Annotation and Data Visualization using Gviz |
PWMEnrich | Diego Diez | PWM enrichment analysis |
pwOmics | Maren Sitte | Pathway-based data integration of omics data |
pwrEWAS | Stefan Graw | A user-friendly tool for comprehensive power estimation for epigenome wide association studies (EWAS) |
qckitfastq | August Guang | FASTQ Quality Control |
qcmetrics | Laurent Gatto | A Framework for Quality Control |
QDNAseq | Daoud Sie | Quantitative DNA Sequencing for Chromosomal Aberrations |
qpcrNorm | Jessica Mar | Data-driven normalization strategies for high-throughput qPCR data. |
qpgraph | Robert Castelo | Estimation of genetic and molecular regulatory networks from high-throughput genomics data |
qPLEXanalyzer | Ashley Sawle | Tools for qPLEX-RIME data analysis |
qrqc | Vince Buffalo | Quick Read Quality Control |
qsea | Matthias Lienhard | IP-seq data analysis and vizualization |
qsmooth | Stephanie C. Hicks | Smooth quantile normalization |
QSutils | Mercedes Guerrero-Murillo | Quasispecies Diversity |
Qtlizer | Matthias Munz | Qtlizer: comprehensive QTL annotation of GWAS results |
QUALIFIER | Mike Jiang | Quality Control of Gated Flow Cytometry Experiments |
quantro | Stephanie Hicks | A test for when to use quantile normalization |
quantsmooth | Jan Oosting | Quantile smoothing and genomic visualization of array data |
QuartPAC | Gregory Ryslik | Identification of mutational clusters in protein quaternary structures. |
QuasR | Michael Stadler | Quantify and Annotate Short Reads in R |
QuaternaryProd | Carl Tony Fakhry | Computes the Quaternary Dot Product Scoring Statistic for Signed and Unsigned Causal Graphs |
QUBIC | Yu Zhang | An R package for qualitative biclustering in support of gene co-expression analyses |
qusage | Christopher Bolen | qusage: Quantitative Set Analysis for Gene Expression |
qvalue | John D. Storey, Andrew J. Bass | Q-value estimation for false discovery rate control |
R3CPET | Mohamed Nadhir Djekidel | 3CPET: Finding Co-factor Complexes in Chia-PET experiment using a Hierarchical Dirichlet Process |
r3Cseq | Supat Thongjuea or | Analysis of Chromosome Conformation Capture and Next-generation Sequencing (3C-seq) |
R453Plus1Toolbox | Hans-Ulrich Klein | A package for importing and analyzing data from Roche's Genome Sequencer System |
R4RNA | Daniel Lai | An R package for RNA visualization and analysis |
RaggedExperiment | Martin Morgan | Representation of Sparse Experiments and Assays Across Samples |
rain | Paul F. Thaben | Rhythmicity Analysis Incorporating Non-parametric Methods |
rama | Raphael Gottardo | Robust Analysis of MicroArrays |
ramwas | Andrey A Shabalin | Fast Methylome-Wide Association Study Pipeline for Enrichment Platforms |
RandomWalkRestartMH | Alberto Valdeolivas Urbelz | Random walk with restart on multiplex and heterogeneous Networks |
randPack | Robert Gentleman | Randomization routines for Clinical Trials |
randRotation | Peter Hettegger | Random Rotation Methods for High Dimensional Data with Batch Structure |
RankProd | Francesco Del Carratore | Rank Product method for identifying differentially expressed genes with application in meta-analysis |
RareVariantVis | Tomasz Stokowy | A suite for analysis of rare genomic variants in whole genome sequencing data |
Rariant | Julian Gehring | Identification and Assessment of Single Nucleotide Variants through Shifts in Non-Consensus Base Call Frequencies |
RbcBook1 | Vince Carey | Support for Springer monograph on Bioconductor |
RBGL | Bioconductor Package Maintainer | An interface to the BOOST graph library |
RBioinf | Robert Gentleman | RBioinf |
rBiopaxParser | Frank Kramer | Parses BioPax files and represents them in R |
RBM | Dongmei Li | RBM: a R package for microarray and RNA-Seq data analysis |
Rbowtie | Michael Stadler | R bowtie wrapper |
Rbowtie2 | Zheng Wei | An R Wrapper for Bowtie2 and AdapterRemoval |
rbsurv | Soo-heang Eo | Robust likelihood-based survival modeling with microarray data |
Rcade | Jonathan Cairns | R-based analysis of ChIP-seq And Differential Expression - a tool for integrating a count-based ChIP-seq analysis with differential expression summary data |
RCAS | Bora Uyar | RNA Centric Annotation System |
RCASPAR | Douaa Mugahid, Lars Kaderali | A package for survival time prediction based on a piecewise baseline hazard Cox regression model. |
rcellminer | Augustin Luna, Vinodh Rajapakse, Fathi Elloumi | rcellminer: Molecular Profiles, Drug Response, and Chemical Structures for the NCI-60 Cell Lines |
rCGH | Frederic Commo | Comprehensive Pipeline for Analyzing and Visualizing Array-Based CGH Data |
RchyOptimyx | Adrin Jalali, Nima Aghaeepour | Optimyzed Cellular Hierarchies for Flow Cytometry |
RcisTarget | Sara Aibar | RcisTarget: Identify transcription factor binding motifs enriched on a gene list |
RCM | Joris Meys | Fit row-column association models with the negative binomial distribution for the microbiome |
Rcpi | Nan Xiao | Molecular Informatics Toolkit for Compound-Protein Interaction in Drug Discovery |
Rcwl | Qiang Hu | Wrap Command Tools and Pipelines Using CWL |
RcwlPipelines | Qiang Hu | Bioinformatics pipelines based on Rcwl |
RCy3 | Alex Pico | Functions to Access and Control Cytoscape |
RCyjs | Paul Shannon | Display and manipulate graphs in cytoscape.js |
RDAVIDWebService | Cristobal Fresno | An R Package for retrieving data from DAVID into R objects using Web Services API. |
rDGIdb | Thomas Thurnherr | R Wrapper for DGIdb |
Rdisop | Steffen Neumann | Decomposition of Isotopic Patterns |
RDRToolbox | Christoph Bartenhagen | A package for nonlinear dimension reduction with Isomap and LLE. |
ReactomeGSA | Johannes Griss | Client for the Reactome Analysis Service for comparative multi-omics gene set analysis |
ReactomePA | Guangchuang Yu | Reactome Pathway Analysis |
readat | Richard Cotton | Functionality to Read and Manipulate SomaLogic ADAT files |
ReadqPCR | James Perkins | Read qPCR data |
reb | Karl J. Dykema | Regional Expression Biases |
REBET | Bill Wheeler | The subREgion-based BurdEn Test (REBET) |
receptLoss | Daniel Pique | Unsupervised Identification of Genes with Expression Loss in Subsets of Tumors |
reconsi | Joris Meys | Resampling Collapsed Null Distributions for Simultaneous Inference |
recount | Leonardo Collado-Torres | Explore and download data from the recount project |
recoup | Panagiotis Moulos | An R package for the creation of complex genomic profile plots |
RedeR | Mauro Castro | Interactive visualization and manipulation of nested networks |
REDseq | Lihua Julie Zhu | Analysis of high-throughput sequencing data processed by restriction enzyme digestion |
RefNet | Paul Shannon | A queryable collection of molecular interactions, from many sources |
RefPlus | Kai-Ming Chang | A function set for the Extrapolation Strategy (RMA+) and Extrapolation Averaging (RMA++) methods. |
regioneR | Bernat Gel | Association analysis of genomic regions based on permutation tests |
regionReport | Leonardo Collado-Torres | Generate HTML or PDF reports for a set of genomic regions or DESeq2/edgeR results |
regsplice | Lukas M. Weber | L1-regularization based methods for detection of differential splicing |
regutools | Joselyn Chavez | regutools: an R package for data extraction from RegulonDB |
REMP | Yinan Zheng | Repetitive Element Methylation Prediction |
Repitools | Mark Robinson | Epigenomic tools |
ReportingTools | Jason A. Hackney, Gabriel Becker, Jessica L. Larson | Tools for making reports in various formats |
RepViz | Thomas Faux, Asta Laiho | Replicate oriented Visualization of a genomic region |
ReQON | Christopher Cabanski | Recalibrating Quality Of Nucleotides |
restfulSE | Shweta Gopaulakrishnan | Access matrix-like HDF5 server content or BigQuery content through a SummarizedExperiment interface |
rexposome | Carles Hernandez-Ferrer | Exposome exploration and outcome data analysis |
rfaRm | Lara Selles Vidal, Rafael Ayala | An R interface to the Rfam database |
rfPred | Hugo Varet | Assign rfPred functional prediction scores to a missense variants list |
rGADEM | Arnaud Droit | de novo motif discovery |
RGalaxy | Bioconductor Package Maintainer | Make an R function available in the Galaxy web platform |
Rgin | Hector Climente-Gonzalez | gin in R |
RGMQL | Simone Pallotta | GenoMetric Query Language for R/Bioconductor |
RGraph2js | Stephane Cano | Convert a Graph into a D3js Script |
Rgraphviz | Kasper Daniel Hansen | Provides plotting capabilities for R graph objects |
rGREAT | Zuguang Gu | Client for GREAT Analysis |
RGSEA | Chengcheng Ma | Random Gene Set Enrichment Analysis |
rgsepd | Karl Stamm | Gene Set Enrichment / Projection Displays |
rhdf5 | Mike Smith | R Interface to HDF5 |
rhdf5client | Vincent Carey | Access HDF5 content from h5serv |
rhdf5filters | Mike Smith | HDF5 Compression Filters |
Rhdf5lib | Mike Smith | hdf5 library as an R package |
Rhisat2 | Charlotte Soneson | R Wrapper for HISAT2 Aligner |
Rhtslib | Bioconductor Package Maintainer | HTSlib high-throughput sequencing library as an R package |
RiboProfiling | A. Popa | Ribosome Profiling Data Analysis: from BAM to Data Representation and Interpretation |
ribor | Michael Geng | An R Interface for Ribo Files |
riboSeqR | Thomas J. Hardcastle | Analysis of sequencing data from ribosome profiling experiments |
ribosomeProfilingQC | Jianhong Ou | Ribosome Profiling Quality Control |
RImmPort | Zicheng Hu, Ravi Shankar | RImmPort: Enabling Ready-for-analysis Immunology Research Data |
Ringo | J. Toedling | R Investigation of ChIP-chip Oligoarrays |
RIPSeeker | Yue Li | RIPSeeker: a statistical package for identifying protein-associated transcripts from RIP-seq experiments |
Risa | Alejandra Gonzalez-Beltran | Converting experimental metadata from ISA-tab into Bioconductor data structures |
RITAN | Michael Zimmermann | Rapid Integration of Term Annotation and Network resources |
RIVER | Yungil Kim | R package for RIVER (RNA-Informed Variant Effect on Regulation) |
RJMCMCNucleosomes | Astrid Deschênes | Bayesian hierarchical model for genome-wide nucleosome positioning with high-throughput short-read data (MNase-Seq) |
RLMM | Nusrat Rabbee | A Genotype Calling Algorithm for Affymetrix SNP Arrays |
Rmagpie | Camille Maumet | MicroArray Gene-expression-based Program In Error rate estimation |
RMassBank | RMassBank at Eawag | Workflow to process tandem MS files and build MassBank records |
rmelting | J. Aravind | R Interface to MELTING 5 |
RmiR | Francesco Favero | Package to work with miRNAs and miRNA targets with R |
Rmmquant | Zytnicki Matthias | RNA-Seq multi-mapping Reads Quantification Tool |
RNAAgeCalc | Xu Ren | A multi-tissue transcriptional age calculator |
RNAdecay | Reed Sorenson | Maximum Likelihood Decay Modeling of RNA Degradation Data |
RNAinteract | Bernd Fischer | Estimate Pairwise Interactions from multidimensional features |
RNAither | Lars Kaderali | Statistical analysis of high-throughput RNAi screens |
RNAmodR | Felix G.M. Ernst | Detection of post-transcriptional modifications in high throughput sequencing data |
RNAmodR.AlkAnilineSeq | Felix G.M. Ernst | Detection of m7G, m3C and D modification by AlkAnilineSeq |
RNAmodR.ML | Felix G.M. Ernst | Detecting patterns of post-transcriptional modifications using machine learning |
RNAmodR.RiboMethSeq | Felix G.M. Ernst | Detection of 2'-O methylations by RiboMethSeq |
RNAprobR | Nikos Sidiropoulos | An R package for analysis of massive parallel sequencing based RNA structure probing data |
RNAsense | Marcus Rosenblatt | Analysis of Time-Resolved RNA-Seq Data |
rnaseqcomp | Mingxiang Teng | Benchmarks for RNA-seq Quantification Pipelines |
rnaSeqMap | Michal Okoniewski | rnaSeq secondary analyses |
RNASeqPower | Terry M Therneau | Sample size for RNAseq studies |
RNASeqR | Kuan-Hao Chao | RNASeqR: an R package for automated two-group RNA-Seq analysis workflow |
RnBeads | Fabian Mueller | RnBeads |
Rnits | Dipen P. Sangurdekar | R Normalization and Inference of Time Series data |
roar | Elena Grassi | Identify differential APA usage from RNA-seq alignments |
ROC | Vince Carey | utilities for ROC, with microarray focus |
ROCpAI | Juan-Pedro Garcia | Receiver Operating Characteristic Partial Area Indexes for evaluating classifiers |
Roleswitch | Yue Li | Infer miRNA-mRNA interactions using paired expression data from a single sample |
rols | Laurent Gatto | An R interface to the Ontology Lookup Service |
ROntoTools | Calin Voichita | R Onto-Tools suite |
ropls | Etienne A. Thevenot | PCA, PLS(-DA) and OPLS(-DA) for multivariate analysis and feature selection of omics data |
ROSeq | Krishan Gupta | A Rank Based Approach to Modeling Gene Expression |
ROTS | Tomi Suomi | Reproducibility-Optimized Test Statistic |
RPA | Leo Lahti | RPA: Robust Probabilistic Averaging for probe-level analysis |
RProtoBufLib | Mike Jiang, Jake Wagner | C++ headers and static libraries of Protocol buffers |
RpsiXML | Jitao David Zhang | R interface to PSI-MI 2.5 files |
rpx | Laurent Gatto | R Interface to the ProteomeXchange Repository |
Rqc | Welliton Souza | Quality Control Tool for High-Throughput Sequencing Data |
rqt | Ilya Y. Zhbannikov | rqt: utilities for gene-level meta-analysis |
rqubic | Jitao David Zhang | Qualitative biclustering algorithm for expression data analysis in R |
rRDP | Michael Hahsler | Interface to the RDP Classifier |
RRHO | Jonathan Rosenblatt | Inference on agreement between ordered lists |
rrvgo | Sergi Sayols | Reduce + Visualize GO |
Rsamtools | Bioconductor Package Maintainer | Binary alignment (BAM), FASTA, variant call (BCF), and tabix file import |
rsbml | Michael Lawrence | R support for SBML, using libsbml |
rScudo | Matteo Ciciani | Signature-based Clustering for Diagnostic Purposes |
RSeqAn | August Guang | R SeqAn |
Rsubread | Wei Shi, Yang Liao and Gordon K Smyth | Subread Sequence Alignment and Counting for R |
RSVSim | Christoph Bartenhagen | RSVSim: an R/Bioconductor package for the simulation of structural variations |
rSWeeP | Danrley R. Fernandes | Functions to creation of low dimensional comparative matrices of Amino Acid Sequence occurrences |
rTANDEM | Frederic Fournier | Interfaces the tandem protein identification algorithm in R |
RTCA | Jitao David Zhang | Open-source toolkit to analyse data from xCELLigence System (RTCA) |
RTCGA | Marcin Kosinski | The Cancer Genome Atlas Data Integration |
RTCGAToolbox | Marcel Ramos | A new tool for exporting TCGA Firehose data |
RTN | Mauro Castro | RTN: Reconstruction of Transcriptional regulatory Networks and analysis of regulons |
RTNduals | Mauro Castro, Clarice Groeneveld | Analysis of co-regulation and inference of 'dual regulons' |
RTNsurvival | Clarice Groeneveld, Mauro A. A. Castro | Survival analysis using transcriptional networks inferred by the RTN package |
RTopper | Luigi Marchionni | This package is designed to perform Gene Set Analysis across multiple genomic platforms |
rtracklayer | Michael Lawrence | R interface to genome annotation files and the UCSC genome browser |
Rtreemix | Jasmina Bogojeska | Rtreemix: Mutagenetic trees mixture models. |
rTRM | Diego Diez | Identification of transcriptional regulatory modules from PPI networks |
rTRMui | Diego Diez | A shiny user interface for rTRM |
runibic | Patryk Orzechowski | runibic: row-based biclustering algorithm for analysis of gene expression data in R |
RUVcorr | Saskia Freytag | Removal of unwanted variation for gene-gene correlations and related analysis |
RUVnormalize | Laurent Jacob | RUV for normalization of expression array data |
RUVSeq | Davide Risso | Remove Unwanted Variation from RNA-Seq Data |
RVS | Thomas Sherman | Computes estimates of the probability of related individuals sharing a rare variant |
rWikiPathways | Egon Willighagen | rWikiPathways - R client library for the WikiPathways API |
S4Vectors | Bioconductor Package Maintainer | Foundation of vector-like and list-like containers in Bioconductor |
safe | Ludwig Geistlinger | Significance Analysis of Function and Expression |
sagenhaft | Tim Beissbarth | Collection of functions for reading and comparing SAGE libraries |
SAGx | Per Broberg, | Statistical Analysis of the GeneChip |
SAIGEgds | Xiuwen Zheng | Scalable Implementation of Generalized mixed models using GDS files in Phenome-Wide Association Studies |
samExploreR | shailesh tripathi | samExploreR package: high-performance read summarisation to count vectors with avaliability of sequencing depth reduction simulation |
sampleClassifier | Khadija El Amrani | Sample Classifier |
SamSPECTRAL | Habil | Identifies cell population in flow cytometry data. |
sangerseqR | Jonathon Hill | Tools for Sanger Sequencing Data in R |
SANTA | Alex J. Cornish | Spatial Analysis of Network Associations |
sapFinder | Shaohang Xu, Bo Wen | A package for variant peptides detection and visualization in shotgun proteomics. |
sarks | Dennis Wylie | Suffix Array Kernel Smoothing for discovery of correlative sequence motifs and multi-motif domains |
savR | R. Brent Calder | Parse and analyze Illumina SAV files |
SBGNview | Xiaoxi Dong | Overlay omics data onto SBGN pathway diagram |
SBMLR | Tomas Radivoyevitch | SBML-R Interface and Analysis Tools |
SC3 | Vladimir Kiselev | Single-Cell Consensus Clustering |
Scale4C | Carolin Walter | Scale4C: an R/Bioconductor package for scale-space transformation of 4C-seq data |
scAlign | Nelson Johansen | An alignment and integration method for single cell genomics |
SCAN.UPC | Stephen R. Piccolo | Single-channel array normalization (SCAN) and Universal exPression Codes (UPC) |
SCANVIS | Phaedra Agius | SCANVIS - a tool for SCoring, ANnotating and VISualizing splice junctions |
scater | Davis McCarthy | Single-Cell Analysis Toolkit for Gene Expression Data in R |
scBFA | Ruoxin Li | A dimensionality reduction tool using gene detection pattern to mitigate noisy expression profile of scRNA-seq |
SCBN | Yan Zhou | A statistical normalization method and differential expression analysis for RNA-seq data between different species |
scClassify | Yingxin Lin | scClassify: single-cell Hierarchical Classification |
scDblFinder | Pierre-Luc Germain | scDblFinder |
scDD | Keegan Korthauer | Mixture modeling of single-cell RNA-seq data to identify genes with differential distributions |
scde | Jean Fan | Single Cell Differential Expression |
scds | Dennis Kostka | In-Silico Annotation of Doublets for Single Cell RNA Sequencing Data |
scFeatureFilter | Guillaume Devailly | A correlation-based method for quality filtering of single-cell RNAseq data |
scfind | Vladimir Kiselev | A search tool for single cell RNA-seq data by gene lists |
scGPS | Quan Nguyen | A complete analysis of single cell subpopulations, from identifying subpopulations to analysing their relationship (scGPS = single cell Global Predictions of Subpopulation) |
schex | Saskia Freytag | Hexbin plots for single cell omics data |
scHOT | Shila Ghazanfar | single-cell higher order testing |
ScISI | Tony Chiang | In Silico Interactome |
scMAGeCK | Xiaolong Cheng | Identify genes associated with multiple expression phenotypes in single-cell CRISPR screening data |
scmap | Vladimir Kiselev | A tool for unsupervised projection of single cell RNA-seq data |
scMerge | Kevin Wang | scMerge: Merging multiple batches of scRNA-seq data |
scmeth | Divy Kangeyan | Functions to conduct quality control analysis in methylation data |
SCnorm | Rhonda Bacher | Normalization of single cell RNA-seq data |
scone | Davide Risso | Single Cell Overview of Normalized Expression data |
Sconify | Tyler J Burns | A toolkit for performing KNN-based statistics for flow and mass cytometry data |
SCOPE | Rujin Wang | A normalization and copy number estimation method for single-cell DNA sequencing |
scoreInvHap | Carlos Ruiz | Get inversion status in predefined regions |
scPCA | Philippe Boileau | Sparse Contrastive Principal Component Analysis |
scPipe | Luyi Tian | pipeline for single cell RNA-seq data analysis |
scran | Aaron Lun | Methods for Single-Cell RNA-Seq Data Analysis |
scRecover | Zhun Miao | scRecover for imputation of single-cell RNA-seq data |
scruff | Zhe Wang | Single Cell RNA-Seq UMI Filtering Facilitator (scruff) |
scry | F. William Townes | Small-Count Analysis Methods for High-Dimensional Data |
scsR | Andrea Franceschini, Roger Meier, Christian von Mering | SiRNA correction for seed mediated off-target effect |
scTensor | Koki Tsuyuzaki | Detection of cell-cell interaction from single-cell RNA-seq dataset by tensor decomposition |
scTGIF | Koki Tsuyuzaki | Cell type annotation for unannotated single-cell RNA-Seq data |
scTHI | Michele Ceccarelli | Indentification of significantly activated ligand-receptor interactions across clusters of cells from single-cell RNA sequencing data |
SDAMS | Yuntong Li | Differential Abundant Analysis for Metabolomics and Proteomics Data |
segmentSeq | Thomas J. Hardcastle | Methods for identifying small RNA loci from high-throughput sequencing data |
selectKSigs | Zhi Yang | Selecting the number of mutational signatures using a perplexity-based measure and cross-validation |
SELEX | Harmen J. Bussemaker | Functions for analyzing SELEX-seq data |
SemDist | Ian Gonzalez | Information Accretion-based Function Predictor Evaluation |
semisup | Armin Rauschenberger | Semi-Supervised Mixture Model |
SEPIRA | Yuting Chen | Systems EPigenomics Inference of Regulatory Activity |
seq2pathway | Xinan Yang with contribution from Zhezhen Wang | a novel tool for functional gene-set (or termed as pathway) analysis of next-generation sequencing data |
SeqArray | Xiuwen Zheng | Data management of large-scale whole-genome sequence variant calls |
seqbias | Daniel Jones | Estimation of per-position bias in high-throughput sequencing data |
seqCAT | Erik Fasterius | High Throughput Sequencing Cell Authentication Toolkit |
seqCNA | David Mosen-Ansorena | Copy number analysis of high-throughput sequencing cancer data |
seqcombo | Guangchuang Yu | Visualization Tool for Sequence Recombination and Reassortment |
SeqGSEA | Xi Wang | Gene Set Enrichment Analysis (GSEA) of RNA-Seq Data: integrating differential expression and splicing |
seqLogo | Robert Ivanek | Sequence logos for DNA sequence alignments |
seqPattern | Vanja Haberle | Visualising oligonucleotide patterns and motif occurrences across a set of sorted sequences |
seqplots | Przemyslaw Stempor | An interactive tool for visualizing NGS signals and sequence motif densities along genomic features using average plots and heatmaps |
seqsetvis | Joseph R Boyd | Set Based Visualizations for Next-Gen Sequencing Data |
SeqSQC | Qian Liu | A bioconductor package for sample quality check with next generation sequencing data |
seqTools | Wolfgang Kaisers | Analysis of nucleotide, sequence and quality content on fastq files |
SeqVarTools | Stephanie M. Gogarten | Tools for variant data |
sesame | Wanding Zhou | Tools For Analyzing Illumina Infinium DNA Methylation Arrays |
SEtools | Pierre-Luc Germain | SEtools: tools for working with SummarizedExperiment |
sevenbridges | Nan Xiao | Seven Bridges Platform API Client and Common Workflow Language Tool Builder in R |
sevenC | Jonas Ibn-Salem | Computational Chromosome Conformation Capture by Correlation of ChIP-seq at CTCF motifs |
SGSeq | Leonard Goldstein | Splice event prediction and quantification from RNA-seq data |
SharedObject | Jiefei Wang | Sharing R objects across multiple R processes without memory duplication |
shinyMethyl | Jean-Philippe Fortin | Interactive visualization for Illumina methylation arrays |
shinyTANDEM | Frederic Fournier | Provides a GUI for rTANDEM |
ShortRead | Bioconductor Package Maintainer | FASTQ input and manipulation |
SIAMCAT | Konrad Zych | Statistical Inference of Associations between Microbial Communities And host phenoTypes |
SICtools | Xiaobin Xing | Find SNV/Indel differences between two bam files with near relationship |
sigaR | Wessel N. van Wieringen | Statistics for Integrative Genomics Analyses in R |
SigCheck | Rory Stark | Check a gene signature's prognostic performance against random signatures, known signatures, and permuted data/metadata |
sigFeature | Pijush Das Developer | sigFeature: Significant feature selection using SVM-RFE & t-statistic |
SigFuge | Patrick Kimes | SigFuge |
siggenes | Holger Schwender | Multiple Testing using SAM and Efron's Empirical Bayes Approaches |
sights | Elika Garg | Statistics and dIagnostic Graphs for HTS |
signatureSearch | Yuzhu Duan | Environment for Gene Expression Searching Combined with Functional Enrichment Analysis |
signeR | Renan Valieris | Empirical Bayesian approach to mutational signature discovery |
signet | Alexandre Gouy | signet: Selection Inference in Gene NETworks |
sigPathway | Weil Lai | Pathway Analysis |
SigsPack | Franziska Schumann | Mutational Signature Estimation for Single Samples |
sigsquared | UnJin Lee | Gene signature generation for functionally validated signaling pathways |
SIM | Renee X. de Menezes | Integrated Analysis on two human genomic datasets |
SIMAT | M. R. Nezami Ranjbar | GC-SIM-MS data processing and alaysis tool |
SimBindProfiles | Bettina Fischer | Similar Binding Profiles |
SIMD | Jiadi Zhu | Statistical Inferences with MeDIP-seq Data (SIMD) to infer the methylation level for each CpG site |
SimFFPE | Lanying Wei | NGS Read Simulator for FFPE Tissue |
similaRpeak | Astrid Deschenes | Metrics to estimate a level of similarity between two ChIP-Seq profiles |
SIMLR | Luca De Sano | Single-cell Interpretation via Multi-kernel LeaRning (SIMLR) |
simpleaffy | Crispin Miller | Very simple high level analysis of Affymetrix data |
simulatorZ | Yuqing Zhang | Simulator for Collections of Independent Genomic Data Sets |
sincell | Miguel Julia, Antonio Rausell | R package for the statistical assessment of cell state hierarchies from single-cell RNA-seq data |
SingleCellExperiment | Davide Risso | S4 Classes for Single Cell Data |
SingleCellSignalR | Jacques Colinge | Cell Signalling Using Single Cell RNAseq Data Analysis |
singleCellTK | David Jenkins | Interactive Analysis of Single Cell RNA-Seq Data |
SingleR | Aaron Lun | Reference-Based Single-Cell RNA-Seq Annotation |
singscore | Dharmesh D. Bhuva | Rank-based single-sample gene set scoring method |
SISPA | Bhakti Dwivedi | SISPA: Method for Sample Integrated Set Profile Analysis |
sitePath | Chengyang Ji | Detection of sites with fixation of amino acid substitutions in protein evolution |
sizepower | Weiliang Qiu | Sample Size and Power Calculation in Micorarray Studies |
skewr | Ryan Putney | Visualize Intensities Produced by Illumina's Human Methylation 450k BeadChip |
slalom | Davis McCarthy | Factorial Latent Variable Modeling of Single-Cell RNA-Seq Data |
SLGI | Nolwenn Le Meur | Synthetic Lethal Genetic Interaction |
slingshot | Kelly Street | Tools for ordering single-cell sequencing |
slinky | Eric J. Kort | Putting the fun in LINCS L1000 data analysis |
SLqPCR | Matthias Kohl | Functions for analysis of real-time quantitative PCR data at SIRS-Lab GmbH |
SMAD | Qingzhou Zhang | Statistical Modelling of AP-MS Data (SMAD) |
SMAP | Robin Andersson | A Segmental Maximum A Posteriori Approach to Array-CGH Copy Number Profiling |
SMITE | Neil Ari Wijetunga, Andrew Damon Johnston | Significance-based Modules Integrating the Transcriptome and Epigenome |
SNAGEE | David Venet | Signal-to-Noise applied to Gene Expression Experiments |
snapCGH | John Marioni | Segmentation, normalisation and processing of aCGH data |
snapcount | Rone Charles | R/Bioconductor Package for interfacing with Snaptron for rapid querying of expression counts |
snm | John D. Storey | Supervised Normalization of Microarrays |
SNPediaR | David Montaner | Query data from SNPedia |
SNPhood | Christian Arnold | SNPhood: Investigate, quantify and visualise the epigenomic neighbourhood of SNPs using NGS data |
SNPRelate | Xiuwen Zheng | Parallel Computing Toolset for Relatedness and Principal Component Analysis of SNP Data |
snpStats | David Clayton | SnpMatrix and XSnpMatrix classes and methods |
soGGi | Tom Carroll | Visualise ChIP-seq, MNase-seq and motif occurrence as aggregate plots Summarised Over Grouped Genomic Intervals |
sojourner | Sojourner Developer | Statistical analysis of single molecule trajectories |
SomaticSignatures | Julian Gehring | Somatic Signatures |
SpacePAC | Gregory Ryslik | Identification of Mutational Clusters in 3D Protein Space via Simulation. |
Spaniel | Rachel Queen | Spatial Transcriptomics Analysis |
sparseDOSSA | Boyu Ren, Emma Schwager, George Weingart | Sparse Data Observations for Simulating Synthetic Abundance |
sparseMatrixStats | Constantin Ahlmann-Eltze | Summary Statistics for Rows and Columns of Sparse Matrices |
sparsenetgls | Irene SL Zeng | Using Gaussian graphical structue learning estimation in generalized least squared regression for multivariate normal regression |
SparseSignatures | Luca De Sano | SparseSignatures |
SpatialCPie | Joseph Bergenstraahle | Cluster analysis of Spatial Transcriptomics data |
specL | Christian Panse | specL - Prepare Peptide Spectrum Matches for Use in Targeted Proteomics |
SpeCond | Florence Cavalli | Condition specific detection from expression data |
SpectralTAD | Kellen Cresswell | SpectralTAD: Hierarchical TAD detection using spectral clustering |
SPEM | Xinyi YANG | S-system parameter estimation method |
SPIA | Adi Laurentiu Tarca | Signaling Pathway Impact Analysis (SPIA) using combined evidence of pathway over-representation and unusual signaling perturbations |
spicyR | Ellis Patrick | Spatial analysis of in situ cytometry data |
SpidermiR | Claudia Cava | SpidermiR: An R/Bioconductor package for integrative network analysis with miRNA data |
spikeLI | Enrico Carlon | Affymetrix Spike-in Langmuir Isotherm Data Analysis Tool |
spkTools | Matthew N McCall | Methods for Spike-in Arrays |
splatter | Luke Zappia | Simple Simulation of Single-cell RNA Sequencing Data |
splicegear | Laurent Gautier | splicegear |
SplicingGraphs | H. Pagès | Create, manipulate, visualize splicing graphs, and assign RNA-seq reads to them |
splineTimeR | Herbert Braselmann, Martin Selmansberger | Time-course differential gene expression data analysis using spline regression models followed by gene association network reconstruction |
SPLINTER | Diana Low | Splice Interpreter of Transcripts |
splots | Wolfgang Huber | Visualization of high-throughput assays in microtitre plate or slide format |
SPONGE | Markus List | Sparse Partial Correlations On Gene Expression |
spotSegmentation | Chris Fraley | Microarray Spot Segmentation and Gridding for Blocks of Microarray Spots |
spqn | Yi Wang | Spatial quantile normalization |
SQLDataFrame | Qian Liu | Representation of SQL database in DataFrame metaphor |
SQUADD | Martial Sankar | Add-on of the SQUAD Software |
sRACIPE | Vivek Kohar | Systems biology tool to simulate gene regulatory circuits |
SRAdb | Jack Zhu | A compilation of metadata from NCBI SRA and tools |
sRAP | Charles Warden | Simplified RNA-Seq Analysis Pipeline |
SRGnet | Isar Nassiri | SRGnet: An R package for studying synergistic response to gene mutations from transcriptomics data |
srnadiff | Zytnicki Matthias | Finding differentially expressed unannotated genomic regions from RNA-seq data |
sscore | Richard Kennedy | S-Score Algorithm for Affymetrix Oligonucleotide Microarrays |
sscu | Yu Sun | Strength of Selected Codon Usage |
sSeq | Danni Yu | Shrinkage estimation of dispersion in Negative Binomial models for RNA-seq experiments with small sample size |
ssize | Gregory R. Warnes | Estimate Microarray Sample Size |
SSPA | Maarten van Iterson | General Sample Size and Power Analysis for Microarray and Next-Generation Sequencing Data |
ssPATHS | Natalie R. Davidson | ssPATHS: Single Sample PATHway Score |
ssrch | VJ Carey | a simple search engine |
ssviz | Diana Low | A small RNA-seq visualizer and analysis toolkit |
stageR | Koen Van den Berge | stageR: stage-wise analysis of high throughput gene expression data in R |
STAN | Rafael Campos-Martin | The Genomic STate ANnotation Package |
staRank | Juliane Siebourg | Stability Ranking |
StarBioTrek | Claudia Cava | StarBioTrek |
Starr | Benedikt Zacher | Simple tiling array analysis of Affymetrix ChIP-chip data |
STATegRa | David Gomez-Cabrero, Núria Planell | Classes and methods for multi-omics data integration |
statTarget | Hemi Luan | Statistical Analysis of Molecular Profiles |
stepNorm | Yuanyuan Xiao | Stepwise normalization functions for cDNA microarrays |
strandCheckR | Thu-Hien To | Calculate strandness information of a bam file |
Streamer | Martin Morgan | Enabling stream processing of large files |
STRINGdb | Damian Szklarczyk | STRINGdb (Search Tool for the Retrieval of Interacting proteins database) |
STROMA4 | Sadiq Saleh | Assign Properties to TNBC Patients |
struct | Gavin Rhys Lloyd | Statistics in R Using Class-based Templates |
Structstrings | Felix G.M. Ernst | Implementation of the dot bracket annotations with Biostrings |
structToolbox | Gavin Rhys Lloyd | Data processing & analysis tools for Metabolomics and other omics |
StructuralVariantAnnotation | Daniel Cameron | Variant annotations for structural variants |
SubCellBarCode | Taner Arslan | SubCellBarCode: Integrated workflow for robust mapping and visualizing whole human spatial proteome |
subSeq | Andrew J. Bass, John D. Storey | Subsampling of high-throughput sequencing count data |
SummarizedBenchmark | Patrick Kimes | Classes and methods for performing benchmark comparisons |
SummarizedExperiment | Bioconductor Package Maintainer | SummarizedExperiment container |
supraHex | Hai Fang | supraHex: a supra-hexagonal map for analysing tabular omics data |
survcomp | Benjamin Haibe-Kains, Markus Schroeder, Catharina Olsen | Performance Assessment and Comparison for Survival Analysis |
survtype | Dongmin Jung | Subtype Identification with Survival Data |
Sushi | Douglas H Phanstiel | Tools for visualizing genomics data |
sva | Jeffrey T. Leek, John D. Storey, W. Evan Johnson | Surrogate Variable Analysis |
SVAPLSseq | Sutirtha Chakraborty | SVAPLSseq-An R package to estimate the hidden factors of unwanted variability and adjust for them to enable a more powerful and accurate differential expression analysis based on RNAseq data |
SWATH2stats | Peter Blattmann | Transform and Filter SWATH Data for Statistical Packages |
SwathXtend | Jemma Wu | SWATH extended library generation and statistical data analysis |
swfdr | Simina M. Boca, Jeffrey T. Leek | Science-wise false discovery rate and proportion of true null hypotheses estimation |
SwimR | Randy Blakely | SwimR: A Suite of Analytical Tools for Quantification of C. elegans Swimming Behavior |
switchBox | Bahman Afsari, Luigi Marchionni, Wikum Dinalankara | Utilities to train and validate classifiers based on pair switching using the K-Top-Scoring-Pair (KTSP) algorithm |
switchde | Kieran Campbell | Switch-like differential expression across single-cell trajectories |
synapter | Laurent Gatto and Sebastian Gibb | Label-free data analysis pipeline for optimal identification and quantitation |
synergyfinder | Shuyu Zheng | Calculate and Visualize Synergy Scores for Drug Combinations |
SynExtend | Nicholas Cooley | Tools for Working With Synteny Objects |
synlet | Chunxuan Shao | Hits Selection for Synthetic Lethal RNAi Screen Data |
SynMut | Haogao Gu | SynMut: Designing Synonymously Mutated Sequences with Different Genomic Signatures |
systemPipeR | Thomas Girke | systemPipeR: NGS workflow and report generation environment |
TAPseq | Andreas Gschwind | Targeted scRNA-seq primer design for TAP-seq |
target | Mahmoud Ahmed | Predict Combined Function of Transcription Factors |
TargetScore | Yue Li | TargetScore: Infer microRNA targets using microRNA-overexpression data and sequence information |
TargetSearch | Alvaro Cuadros-Inostroza | A package for the analysis of GC-MS metabolite profiling data |
TarSeqQC | Gabriela Merino | TARgeted SEQuencing Experiment Quality Control |
TBSignatureProfiler | David Jenkins | Profile RA-Seq Data Using TB Pathway Signatures |
TCC | Jianqiang Sun, Tomoaki Nishiyama | TCC: Differential expression analysis for tag count data with robust normalization strategies |
TCGAbiolinks | Tiago Chedraoui Silva, Antonio Colaprico | TCGAbiolinks: An R/Bioconductor package for integrative analysis with GDC data |
TCGAbiolinksGUI | Tiago C. Silva | "TCGAbiolinksGUI: A Graphical User Interface to analyze cancer molecular and clinical data" |
TCGAutils | Marcel Ramos | TCGA utility functions for data management |
TCseq | Mengjun Wu | Time course sequencing data analysis |
TDARACNE | Zoppoli Pietro | Network reverse engineering from time course data. |
tenXplore | VJ Carey | ontological exploration of scRNA-seq of 1.3 million mouse neurons from 10x genomics |
TEQC | Manuela Hummel | Quality control for target capture experiments |
ternarynet | Matthew N. McCall | Ternary Network Estimation |
TFARM | Liuba Nausicaa Martino | Transcription Factors Association Rules Miner |
TFBSTools | Ge Tan | Software Package for Transcription Factor Binding Site (TFBS) Analysis |
TFEA.ChIP | Laura Puente Santamaría | Analyze Transcription Factor Enrichment |
TFHAZ | Alberto Marchesi | Transcription Factor High Accumulation Zones |
TFutils | Shweta Gopaulakrishnan | TFutils |
tidybulk | Stefano Mangiola | Brings transcriptomics to the tidyverse |
tigre | Antti Honkela | Transcription factor Inference through Gaussian process Reconstruction of Expression |
tilingArray | Zhenyu Xu | Transcript mapping with high-density oligonucleotide tiling arrays |
timecourse | Yu Chuan Tai | Statistical Analysis for Developmental Microarray Time Course Data |
timeOmics | Antoine Bodein | Time-Course Multi-Omics data integration |
timescape | Maia Smith | Patient Clonal Timescapes |
TimeSeriesExperiment | Lan Huong Nguyen | Analysis for short time-series data |
TIN | Bjarne Johannessen | Transcriptome instability analysis |
TissueEnrich | Ashish Jain | Tissue-specific gene enrichment analysis |
TitanCNA | Gavin Ha | Subclonal copy number and LOH prediction from whole genome sequencing of tumours |
tkWidgets | J. Zhang | R based tk widgets |
TMixClust | Monica Golumbeanu | Time Series Clustering of Gene Expression with Gaussian Mixed-Effects Models and Smoothing Splines |
TNBC.CMS | Doyeong Yu | TNBC.CMS: Prediction of TNBC Consensus Molecular Subtypes |
TnT | Jialin Ma | Interactive Visualization for Genomic Features |
TOAST | Ziyi Li | Tools for the analysis of heterogeneous tissues |
tofsims | Lorenz Gerber | Import, process and analysis of Time-of-Flight Secondary Ion Mass Spectrometry (ToF-SIMS) imaging data |
ToPASeq | Ivana Ihnatova | Topology-based pathway analysis of RNA-seq data |
topconfects | Paul Harrison | Top Confident Effect Sizes |
topdownr | Sebastian Gibb | Investigation of Fragmentation Conditions in Top-Down Proteomics |
topGO | Adrian Alexa | Enrichment Analysis for Gene Ontology |
TPP | Dorothee Childs | Analyze thermal proteome profiling (TPP) experiments |
TPP2D | Nils Kurzawa | Detection of ligand-protein interactions from 2D thermal profiles (DLPTP) |
tracktables | Tom Carroll | Build IGV tracks and HTML reports |
trackViewer | Jianhong Ou | A R/Bioconductor package with web interface for drawing elegant interactive tracks or lollipop plot to facilitate integrated analysis of multi-omics data |
tradeSeq | Hector Roux de Bezieux | trajectory-based differential expression analysis for sequencing data |
transcriptogramer | Diego Morais | Transcriptional analysis based on transcriptograms |
transcriptR | Armen R. Karapetyan | An Integrative Tool for ChIP- And RNA-Seq Based Primary Transcripts Detection and Quantification |
transite | Konstantin Krismer | RNA-binding protein motif analysis |
tRanslatome | Toma Tebaldi, Erik Dassi | Comparison between multiple levels of gene expression |
TransView | Julius Muller | Read density map construction and accession. Visualization of ChIPSeq and RNASeq data sets |
traseR | li chen | GWAS trait-associated SNP enrichment analyses in genomic intervals |
TreeAndLeaf | Milena Cardoso | An alternative to dendrogram visualization and insertion of multiple layers of information |
treeio | Guangchuang Yu | Base Classes and Functions for Phylogenetic Tree Input and Output |
TreeSummarizedExperiment | Ruizhu Huang | TreeSummarizedExperiment: a S4 Class for Data with Tree Structures |
trena | Paul Shannon | Fit transcriptional regulatory networks using gene expression, priors, machine learning |
Trendy | Rhonda Bacher | Breakpoint analysis of time-course expression data |
triform | Thomas Carroll | Triform finds enriched regions (peaks) in transcription factor ChIP-sequencing data |
trigger | John D. Storey | Transcriptional Regulatory Inference from Genetics of Gene ExpRession |
trio | Holger Schwender | Testing of SNPs and SNP Interactions in Case-Parent Trio Studies |
triplex | Jiri Hon | Search and visualize intramolecular triplex-forming sequences in DNA |
tRNA | Felix GM Ernst | Analyzing tRNA sequences and structures |
tRNAdbImport | Felix G.M. Ernst | Importing from tRNAdb and mitotRNAdb as GRanges objects |
tRNAscanImport | Felix G.M. Ernst | Importing a tRNAscan-SE result file as GRanges object |
TRONCO | Luca De Sano | TRONCO, an R package for TRanslational ONCOlogy |
TSCAN | Zhicheng Ji | TSCAN: Tools for Single-Cell ANalysis |
tscR | Pérez-Sanz, Fernando | A time series clustering package combining slope and Frechet distances |
tspair | Jeffrey T. Leek | Top Scoring Pairs for Microarray Classification |
TSRchitect | R. Taylor Raborn | Promoter identification from large-scale TSS profiling data |
TTMap | Rachel Jeitziner | Two-Tier Mapper: a clustering tool based on topological data analysis |
TurboNorm | Maarten van Iterson | A fast scatterplot smoother suitable for microarray normalization |
TVTB | Kevin Rue-Albrecht | TVTB: The VCF Tool Box |
tweeDEseq | Juan R Gonzalez | RNA-seq data analysis using the Poisson-Tweedie family of distributions |
twilight | Stefanie Scheid | Estimation of local false discovery rate |
twoddpcr | Anthony Chiu | Classify 2-d Droplet Digital PCR (ddPCR) data and quantify the number of starting molecules |
tximeta | Michael Love | Transcript Quantification Import with Automatic Metadata |
tximport | Michael Love | Import and summarize transcript-level estimates for transcript- and gene-level analysis |
TxRegInfra | VJ Carey | Metadata management for multiomic specification of transcriptional regulatory networks |
TypeInfo | Duncan Temple Lang | Optional Type Specification Prototype |
Ularcirc | David Humphreys | Shiny app for canonical and back splicing analysis (i.e. circular and mRNA analysis) |
UNDO | Niya Wang | Unsupervised Deconvolution of Tumor-Stromal Mixed Expressions |
unifiedWMWqPCR | Joris Meys | Unified Wilcoxon-Mann Whitney Test for testing differential expression in qPCR data |
UniProt.ws | Bioconductor Package Maintainer | R Interface to UniProt Web Services |
Uniquorn | 'Raik Otto' | Identification of cancer cell lines based on their weighted mutational/ variational fingerprint |
universalmotif | Benjamin Jean-Marie Tremblay | Import, Modify, and Export Motifs with R |
uSORT | Hao Chen | uSORT: A self-refining ordering pipeline for gene selection |
VanillaICE | Robert Scharpf | A Hidden Markov Model for high throughput genotyping arrays |
variancePartition | Gabriel E. Hoffman | Quantify and interpret divers of variation in multilevel gene expression experiments |
VariantAnnotation | Bioconductor Package Maintainer | Annotation of Genetic Variants |
VariantExperiment | Qian Liu | A RangedSummarizedExperiment Container for VCF/GDS Data with GDS Backend |
VariantFiltering | Robert Castelo | Filtering of coding and non-coding genetic variants |
VariantTools | Michael Lawrence | Tools for Exploratory Analysis of Variant Calls |
vasp | Huihui Yu | Quantification and Visulization of Variations of Splicing in Population |
vbmp | Nicola Lama | Variational Bayesian Multinomial Probit Regression |
VCFArray | Qian Liu | Representing on-disk / remote VCF files as array-like objects |
Vega | Sandro Morganella | An R package for copy number data segmentation |
VegaMC | Sandro Morganella | VegaMC: A Package Implementing a Variational Piecewise Smooth Model for Identification of Driver Chromosomal Imbalances in Cancer |
VennDetail | Kai Guo | A package for visualization and extract details |
vidger | Brandon Monier | Create rapid visualizations of RNAseq data in R |
viper | Mariano J Alvarez | Virtual Inference of Protein-activity by Enriched Regulon analysis |
ViSEAGO | Aurelien Brionne | ViSEAGO: a Bioconductor package for clustering biological functions using Gene Ontology and semantic similarity |
vsn | Wolfgang Huber | Variance stabilization and calibration for microarray data |
vtpnet | VJ Carey | variant-transcription factor-phenotype networks |
vulcan | Federico M. Giorgi | VirtUaL ChIP-Seq data Analysis using Networks |
waddR | Julian Flesch | Statistical tests for detecting differential distributions based on the 2-Wasserstein distance |
wateRmelon | Leo | Illumina 450 methylation array normalization and metrics |
wavClusteR | Federico Comoglio | Sensitive and highly resolved identification of RNA-protein interaction sites in PAR-CLIP data |
waveTiling | Kristof De Beuf | Wavelet-Based Models for Tiling Array Transcriptome Analysis |
weaver | Seth Falcon | Tools and extensions for processing Sweave documents |
webbioc | Colin A. Smith | Bioconductor Web Interface |
weitrix | Paul Harrison | Weighted matrix manipulation, finding components of variation with weighted or sparse data |
widgetTools | Jianhua Zhang | Creates an interactive tcltk widget |
wiggleplotr | Kaur Alasoo | Make read coverage plots from BigWig files |
Wrench | Hector Corrada Bravo | Wrench normalization for sparse count data |
XBSeq | Yuanhang Liu | Test for differential expression for RNA-seq data |
XCIR | Renan Sauteraud | XCI-inference |
xcms | Steffen Neumann | LC-MS and GC-MS Data Analysis |
XDE | Robert Scharpf | XDE: a Bayesian hierarchical model for cross-study analysis of differential gene expression |
Xeva | Benjamin Haibe-Kains | Analysis of patient-derived xenograft (PDX) data |
XINA | Lang Ho Lee and Sasha A. Singh | Multiplexes Isobaric Mass Tagged-based Kinetics Data for Network Analysis |
xmapbridge | Chris Wirth | Export plotting files to the xmapBridge for visualisation in X:Map |
xps | Christian Stratowa | Processing and Analysis of Affymetrix Oligonucleotide Arrays including Exon Arrays, Whole Genome Arrays and Plate Arrays |
XVector | Hervé Pagès | Foundation of external vector representation and manipulation in Bioconductor |
yamss | Leslie Myint | Tools for high-throughput metabolomics |
YAPSA | Daniel Huebschmann | Yet Another Package for Signature Analysis |
yaqcaffy | Laurent Gatto | Affymetrix expression data quality control and reproducibility analysis |
yarn | Joseph N Paulson | YARN: Robust Multi-Condition RNA-Seq Preprocessing and Normalization |
zFPKM | Ron Ammar | A suite of functions to facilitate zFPKM transformations |
zinbwave | Davide Risso | Zero-Inflated Negative Binomial Model for RNA-Seq Data |
zlibbioc | Bioconductor Package Maintainer | An R packaged zlib-1.2.5 |