Introduction to derfinderPlot
24 October 2023
Package
derfinderPlot 1.36.0
1 Basics
1.1 Install derfinderPlot
R is an open-source statistical environment which can be easily modified to enhance its functionality via packages. derfinderPlot is a R package available via the Bioconductor repository for packages. R can be installed on any operating system from CRAN after which you can install derfinderPlot by using the following commands in your R session:
if (!requireNamespace("BiocManager", quietly = TRUE)) {
install.packages("BiocManager")
}
BiocManager::install("derfinderPlot")
## Check that you have a valid Bioconductor installation
BiocManager::valid()1.2 Required knowledge
derfinderPlot is based on many other packages and in particular in those that have implemented the infrastructure needed for dealing with RNA-seq data. A derfinderPlot user is not expected to deal with those packages directly but will need to be familiar with derfinder and for some plots with ggbio.
If you are asking yourself the question “Where do I start using Bioconductor?” you might be interested in this blog post.
1.3 Asking for help
As package developers, we try to explain clearly how to use our packages and in which order to use the functions. But R and Bioconductor have a steep learning curve so it is critical to learn where to ask for help. The blog post quoted above mentions some but we would like to highlight the Bioconductor support site as the main resource for getting help: remember to use the derfinder or derfinderPlot tags and check the older posts. Other alternatives are available such as creating GitHub issues and tweeting. However, please note that if you want to receive help you should adhere to the posting guidelines. It is particularly critical that you provide a small reproducible example and your session information so package developers can track down the source of the error.
1.4 Citing derfinderPlot
We hope that derfinderPlot will be useful for your research. Please use the following information to cite the package and the overall approach. Thank you!
## Citation info
citation("derfinderPlot")## To cite package 'derfinderPlot' in publications use:
##
## Collado-Torres L, Jaffe AE, Leek JT (2017). _derfinderPlot: Plotting
## functions for derfinder_. doi:10.18129/B9.bioc.derfinderPlot
## <https://doi.org/10.18129/B9.bioc.derfinderPlot>,
## https://github.com/leekgroup/derfinderPlot - R package version
## 1.36.0, <http://www.bioconductor.org/packages/derfinderPlot>.
##
## Collado-Torres L, Nellore A, Frazee AC, Wilks C, Love MI, Langmead B,
## Irizarry RA, Leek JT, Jaffe AE (2017). "Flexible expressed region
## analysis for RNA-seq with derfinder." _Nucl. Acids Res._.
## doi:10.1093/nar/gkw852 <https://doi.org/10.1093/nar/gkw852>,
## <http://nar.oxfordjournals.org/content/early/2016/09/29/nar.gkw852>.
##
## To see these entries in BibTeX format, use 'print(<citation>,
## bibtex=TRUE)', 'toBibtex(.)', or set
## 'options(citation.bibtex.max=999)'.2 Introduction to derfinderPlot
derfinderPlot (Collado-Torres, Jaffe, and Leek, 2017) is an addon package for derfinder (Collado-Torres, Nellore, Frazee, Wilks, Love, Langmead, Irizarry, Leek, and Jaffe, 2017) with functions that allow you to visualize the results.
While the functions in derfinderPlot assume you generated the data with derfinder, they can be used with other GRanges objects properly formatted.
The functions in derfinderPlot are:
plotCluster()is a tailored ggbio (Yin, Cook, and Lawrence, 2012) plot that shows all the regions in a cluster (defined by distance). It shows the base-level coverage for each sample as well as the mean for each group. If these regions overlap any known gene, the gene and the transcript annotation is displayed.plotOverview()is another tailored ggbio (Yin, Cook, and Lawrence, 2012) plot showing an overview of the whole genome. This plot can be useful to observe if the regions are clustered in a subset of a chromosome. It can also be used to check whether the regions match predominantly one part of the gene structure (for example, 3’ overlaps).plotRegionCoverage()is a fast plotting function usingRbase graphics that shows the base-level coverage for each sample inside a specific region of the genome. If the region overlaps any known gene or intron, the information is displayed. Optionally, it can display the known transcripts. This function is most likely the easiest to use withGRangesobjects from other packages.
3 Example
As an example, we will analyze a small subset of the samples from the BrainSpan Atlas of the Human Brain (BrainSpan, 2011) publicly available data.
We first load the required packages.
## Load libraries
suppressPackageStartupMessages(library("derfinder"))
library("derfinderData")
library("derfinderPlot")## Registered S3 method overwritten by 'GGally':
## method from
## +.gg ggplot23.1 Analyze data
For this example, we created a small table with the relevant phenotype data for 12 samples: 6 from fetal samples and 6 from adult samples. We chose at random a brain region, in this case the primary auditory cortex (core) and for the example we will only look at data from chromosome 21. Other variables include the age in years and the gender. The data is shown below.
library("knitr")
## Get pheno table
pheno <- subset(brainspanPheno, structure_acronym == "A1C")
## Display the main information
p <- pheno[, -which(colnames(pheno) %in% c(
"structure_acronym",
"structure_name", "file"
))]
rownames(p) <- NULL
kable(p, format = "html", row.names = TRUE)| gender | lab | Age | group | |
|---|---|---|---|---|
| 1 | M | HSB114.A1C | -0.5192308 | fetal |
| 2 | M | HSB103.A1C | -0.5192308 | fetal |
| 3 | M | HSB178.A1C | -0.4615385 | fetal |
| 4 | M | HSB154.A1C | -0.4615385 | fetal |
| 5 | F | HSB150.A1C | -0.5384615 | fetal |
| 6 | F | HSB149.A1C | -0.5192308 | fetal |
| 7 | F | HSB130.A1C | 21.0000000 | adult |
| 8 | M | HSB136.A1C | 23.0000000 | adult |
| 9 | F | HSB126.A1C | 30.0000000 | adult |
| 10 | M | HSB145.A1C | 36.0000000 | adult |
| 11 | M | HSB123.A1C | 37.0000000 | adult |
| 12 | F | HSB135.A1C | 40.0000000 | adult |
We can load the data from derfinderData (Collado-Torres, Jaffe, and Leek, 2023) by first identifying the paths to the BigWig files with derfinder::rawFiles() and then loading the data with derfinder::fullCoverage().
## Determine the files to use and fix the names
files <- rawFiles(system.file("extdata", "A1C", package = "derfinderData"),
samplepatt = "bw", fileterm = NULL
)
names(files) <- gsub(".bw", "", names(files))
## Load the data from disk
system.time(fullCov <- fullCoverage(files = files, chrs = "chr21"))## 2023-10-24 16:59:04.563912 fullCoverage: processing chromosome chr21## 2023-10-24 16:59:04.582368 loadCoverage: finding chromosome lengths## 2023-10-24 16:59:04.629274 loadCoverage: loading BigWig file /home/biocbuild/bbs-3.18-bioc/R/site-library/derfinderData/extdata/A1C/HSB103.bw## 2023-10-24 16:59:04.886153 loadCoverage: loading BigWig file /home/biocbuild/bbs-3.18-bioc/R/site-library/derfinderData/extdata/A1C/HSB114.bw## 2023-10-24 16:59:05.102246 loadCoverage: loading BigWig file /home/biocbuild/bbs-3.18-bioc/R/site-library/derfinderData/extdata/A1C/HSB123.bw## 2023-10-24 16:59:05.262017 loadCoverage: loading BigWig file /home/biocbuild/bbs-3.18-bioc/R/site-library/derfinderData/extdata/A1C/HSB126.bw## 2023-10-24 16:59:05.376374 loadCoverage: loading BigWig file /home/biocbuild/bbs-3.18-bioc/R/site-library/derfinderData/extdata/A1C/HSB130.bw## 2023-10-24 16:59:05.515562 loadCoverage: loading BigWig file /home/biocbuild/bbs-3.18-bioc/R/site-library/derfinderData/extdata/A1C/HSB135.bw## 2023-10-24 16:59:05.63991 loadCoverage: loading BigWig file /home/biocbuild/bbs-3.18-bioc/R/site-library/derfinderData/extdata/A1C/HSB136.bw## 2023-10-24 16:59:05.758888 loadCoverage: loading BigWig file /home/biocbuild/bbs-3.18-bioc/R/site-library/derfinderData/extdata/A1C/HSB145.bw## 2023-10-24 16:59:05.895081 loadCoverage: loading BigWig file /home/biocbuild/bbs-3.18-bioc/R/site-library/derfinderData/extdata/A1C/HSB149.bw## 2023-10-24 16:59:06.036587 loadCoverage: loading BigWig file /home/biocbuild/bbs-3.18-bioc/R/site-library/derfinderData/extdata/A1C/HSB150.bw## 2023-10-24 16:59:06.151719 loadCoverage: loading BigWig file /home/biocbuild/bbs-3.18-bioc/R/site-library/derfinderData/extdata/A1C/HSB154.bw## 2023-10-24 16:59:07.384562 loadCoverage: loading BigWig file /home/biocbuild/bbs-3.18-bioc/R/site-library/derfinderData/extdata/A1C/HSB178.bw## 2023-10-24 16:59:07.538704 loadCoverage: applying the cutoff to the merged data## 2023-10-24 16:59:07.573951 filterData: originally there were 48129895 rows, now there are 48129895 rows. Meaning that 0 percent was filtered.## user system elapsed
## 2.956 0.100 3.079Alternatively, since the BigWig files are publicly available from BrainSpan (see here), we can extract the relevant coverage data using derfinder::fullCoverage(). Note that as of rtracklayer 1.25.16 BigWig files are not supported on Windows: you can find the fullCov object inside derfinderData to follow the examples.
## Determine the files to use and fix the names
files <- pheno$file
names(files) <- gsub(".A1C", "", pheno$lab)
## Load the data from the web
system.time(fullCov <- fullCoverage(files = files, chrs = "chr21"))Once we have the base-level coverage data for all 12 samples, we can construct the models. In this case, we want to find differences between fetal and adult samples while adjusting for gender and a proxy of the library size.
## Get some idea of the library sizes
sampleDepths <- sampleDepth(collapseFullCoverage(fullCov), 1)## 2023-10-24 16:59:07.655747 sampleDepth: Calculating sample quantiles## 2023-10-24 16:59:07.791658 sampleDepth: Calculating sample adjustments## Define models
models <- makeModels(sampleDepths,
testvars = pheno$group,
adjustvars = pheno[, c("gender")]
)Next, we can find candidate differentially expressed regions (DERs) using as input the segments of the genome where at least one sample has coverage greater than 3. In this particular example, we chose a low theoretical F-statistic cutoff and used 20 permutations.
## Filter coverage
filteredCov <- lapply(fullCov, filterData, cutoff = 3)## 2023-10-24 16:59:08.11299 filterData: originally there were 48129895 rows, now there are 90023 rows. Meaning that 99.81 percent was filtered.## Perform differential expression analysis
suppressPackageStartupMessages(library("bumphunter"))
system.time(results <- analyzeChr(
chr = "chr21", filteredCov$chr21,
models, groupInfo = pheno$group, writeOutput = FALSE,
cutoffFstat = 5e-02, nPermute = 20, seeds = 20140923 + seq_len(20)
))## 2023-10-24 16:59:09.214576 analyzeChr: Pre-processing the coverage data## 2023-10-24 16:59:10.976581 analyzeChr: Calculating statistics## 2023-10-24 16:59:10.979626 calculateStats: calculating the F-statistics## 2023-10-24 16:59:11.176262 analyzeChr: Calculating pvalues## 2023-10-24 16:59:11.176637 analyzeChr: Using the following theoretical cutoff for the F-statistics 5.31765507157871## 2023-10-24 16:59:11.178039 calculatePvalues: identifying data segments## 2023-10-24 16:59:11.186045 findRegions: segmenting information## 2023-10-24 16:59:11.214983 findRegions: identifying candidate regions## 2023-10-24 16:59:11.273557 findRegions: identifying region clusters## 2023-10-24 16:59:11.441683 calculatePvalues: calculating F-statistics for permutation 1 and seed 20140924## 2023-10-24 16:59:11.603903 findRegions: segmenting information## 2023-10-24 16:59:11.643259 findRegions: identifying candidate regions## 2023-10-24 16:59:11.710269 calculatePvalues: calculating F-statistics for permutation 2 and seed 20140925## 2023-10-24 16:59:11.86854 findRegions: segmenting information## 2023-10-24 16:59:11.893472 findRegions: identifying candidate regions## 2023-10-24 16:59:11.954797 calculatePvalues: calculating F-statistics for permutation 3 and seed 20140926## 2023-10-24 16:59:12.105423 findRegions: segmenting information## 2023-10-24 16:59:12.129703 findRegions: identifying candidate regions## 2023-10-24 16:59:12.176423 calculatePvalues: calculating F-statistics for permutation 4 and seed 20140927## 2023-10-24 16:59:12.338141 findRegions: segmenting information## 2023-10-24 16:59:12.362755 findRegions: identifying candidate regions## 2023-10-24 16:59:12.412896 calculatePvalues: calculating F-statistics for permutation 5 and seed 20140928## 2023-10-24 16:59:12.57643 findRegions: segmenting information## 2023-10-24 16:59:12.621103 findRegions: identifying candidate regions## 2023-10-24 16:59:12.669318 calculatePvalues: calculating F-statistics for permutation 6 and seed 20140929## 2023-10-24 16:59:12.832592 findRegions: segmenting information## 2023-10-24 16:59:12.85685 findRegions: identifying candidate regions## 2023-10-24 16:59:12.912262 calculatePvalues: calculating F-statistics for permutation 7 and seed 20140930## 2023-10-24 16:59:13.101609 findRegions: segmenting information## 2023-10-24 16:59:13.126589 findRegions: identifying candidate regions## 2023-10-24 16:59:13.173989 calculatePvalues: calculating F-statistics for permutation 8 and seed 20140931## 2023-10-24 16:59:13.347003 findRegions: segmenting information## 2023-10-24 16:59:13.38247 findRegions: identifying candidate regions## 2023-10-24 16:59:13.429739 calculatePvalues: calculating F-statistics for permutation 9 and seed 20140932## 2023-10-24 16:59:13.597817 findRegions: segmenting information## 2023-10-24 16:59:13.622349 findRegions: identifying candidate regions## 2023-10-24 16:59:13.669635 calculatePvalues: calculating F-statistics for permutation 10 and seed 20140933## 2023-10-24 16:59:13.848437 findRegions: segmenting information## 2023-10-24 16:59:13.87293 findRegions: identifying candidate regions## 2023-10-24 16:59:13.920018 calculatePvalues: calculating F-statistics for permutation 11 and seed 20140934## 2023-10-24 16:59:14.101621 findRegions: segmenting information## 2023-10-24 16:59:14.126059 findRegions: identifying candidate regions## 2023-10-24 16:59:14.172997 calculatePvalues: calculating F-statistics for permutation 12 and seed 20140935## 2023-10-24 16:59:14.350477 findRegions: segmenting information## 2023-10-24 16:59:14.374868 findRegions: identifying candidate regions## 2023-10-24 16:59:14.421143 calculatePvalues: calculating F-statistics for permutation 13 and seed 20140936## 2023-10-24 16:59:14.602552 findRegions: segmenting information## 2023-10-24 16:59:14.627389 findRegions: identifying candidate regions## 2023-10-24 16:59:14.675261 calculatePvalues: calculating F-statistics for permutation 14 and seed 20140937## 2023-10-24 16:59:14.831315 findRegions: segmenting information## 2023-10-24 16:59:14.864029 findRegions: identifying candidate regions## 2023-10-24 16:59:14.911183 calculatePvalues: calculating F-statistics for permutation 15 and seed 20140938## 2023-10-24 16:59:15.065024 findRegions: segmenting information## 2023-10-24 16:59:15.089171 findRegions: identifying candidate regions## 2023-10-24 16:59:15.145927 calculatePvalues: calculating F-statistics for permutation 16 and seed 20140939## 2023-10-24 16:59:15.298666 findRegions: segmenting information## 2023-10-24 16:59:15.323227 findRegions: identifying candidate regions## 2023-10-24 16:59:15.371661 calculatePvalues: calculating F-statistics for permutation 17 and seed 20140940## 2023-10-24 16:59:15.532009 findRegions: segmenting information## 2023-10-24 16:59:15.556061 findRegions: identifying candidate regions## 2023-10-24 16:59:15.602752 calculatePvalues: calculating F-statistics for permutation 18 and seed 20140941## 2023-10-24 16:59:15.76444 findRegions: segmenting information## 2023-10-24 16:59:15.802132 findRegions: identifying candidate regions## 2023-10-24 16:59:15.848841 calculatePvalues: calculating F-statistics for permutation 19 and seed 20140942## 2023-10-24 16:59:16.012673 findRegions: segmenting information## 2023-10-24 16:59:16.037437 findRegions: identifying candidate regions## 2023-10-24 16:59:16.083467 calculatePvalues: calculating F-statistics for permutation 20 and seed 20140943## 2023-10-24 16:59:16.25522 findRegions: segmenting information## 2023-10-24 16:59:16.279406 findRegions: identifying candidate regions## 2023-10-24 16:59:16.35007 calculatePvalues: calculating the p-values## 2023-10-24 16:59:16.435544 analyzeChr: Annotating regions## No annotationPackage supplied. Trying org.Hs.eg.db.## Loading required package: org.Hs.eg.db## Loading required package: AnnotationDbi## Loading required package: stats4## Loading required package: Biobase## Welcome to Bioconductor
##
## Vignettes contain introductory material; view with
## 'browseVignettes()'. To cite Bioconductor, see
## 'citation("Biobase")', and for packages 'citation("pkgname")'.## ## Getting TSS and TSE.## Getting CSS and CSE.## Getting exons.## Annotating genes.## ...## user system elapsed
## 63.019 1.044 64.063## Quick access to the results
regions <- results$regions$regions
## Annotation database to use
suppressPackageStartupMessages(library("TxDb.Hsapiens.UCSC.hg19.knownGene"))
txdb <- TxDb.Hsapiens.UCSC.hg19.knownGene3.2 plotOverview()
Now that we have obtained the main results using derfinder, we can proceed to visualizing the results using derfinderPlot. The easiest to use of all the functions is plotOverview() which takes a set of regions and annotation information produced by bumphunter::matchGenes().
Figure 1 shows the candidate DERs colored by whether their q-value was less than 0.10 or not.
## Q-values overview
plotOverview(regions = regions, annotation = results$annotation, type = "qval")## 2023-10-24 17:00:13.562579 plotOverview: assigning chromosome lengths from hg19!## Scale for x is already present.
## Adding another scale for x, which will replace the existing scale.
## Scale for x is already present.
## Adding another scale for x, which will replace the existing scale.
Figure 1: Location of the DERs in the genome
This plot is was designed for many chromosomes but only one is shown here for simplicity.
Figure 2 shows the candidate DERs colored by the type of gene feature they are nearest too.
## Annotation overview
plotOverview(
regions = regions, annotation = results$annotation,
type = "annotation"
)## 2023-10-24 17:00:16.551806 plotOverview: assigning chromosome lengths from hg19!## Scale for x is already present.
## Adding another scale for x, which will replace the existing scale.
Figure 2: Location of the DERs in the genome and colored by annotation class
This plot is was designed for many chromosomes but only one is shown here for simplicity.
In this particular example, because we are only using data from one chromosome the above plot is not as informative as in a real case scenario. However, with this plot we can quickly observe that nearly all of the candidate DERs are inside an exon.
3.3 plotRegionCoverage()
The complete opposite of visualizing the candidate DERs at the genome-level is to visualize them one region at a time. plotRegionCoverage() allows us to do this quickly for a large number of regions.
Before using this function, we need to process more detailed information using two derfinder functions: annotateRegions() and getRegionCoverage() as shown below.
## Get required information for the plots
annoRegs <- annotateRegions(regions, genomicState$fullGenome)## 2023-10-24 17:00:17.479945 annotateRegions: counting## 2023-10-24 17:00:17.616705 annotateRegions: annotatingregionCov <- getRegionCoverage(fullCov, regions)## 2023-10-24 17:00:17.771278 getRegionCoverage: processing chr21## 2023-10-24 17:00:17.836839 getRegionCoverage: done processing chr21Once we have the relevant information we can proceed to plotting the first 10 regions. In this case, we will supply plotRegionCoverage() with the information it needs to plot transcripts overlapping these 10 regions (Figures ??, ??, ??, ??, ??, ??, ??, ??, ??, ??).
## Plot top 10 regions
plotRegionCoverage(
regions = regions, regionCoverage = regionCov,
groupInfo = pheno$group, nearestAnnotation = results$annotation,
annotatedRegions = annoRegs, whichRegions = 1:10, txdb = txdb, scalefac = 1,
ask = FALSE, verbose = FALSE
)
Figure 3: Base-pair resolution plot of differentially expressed region 1
Figure 4: Base-pair resolution plot of differentially expressed region 2
Figure 5: Base-pair resolution plot of differentially expressed region 3
Figure 6: Base-pair resolution plot of differentially expressed region 4
Figure 7: Base-pair resolution plot of differentially expressed region 5
Figure 8: Base-pair resolution plot of differentially expressed region 6
Figure 9: Base-pair resolution plot of differentially expressed region 7
Figure 10: Base-pair resolution plot of differentially expressed region 8
Figure 11: Base-pair resolution plot of differentially expressed region 9
Figure 12: Base-pair resolution plot of differentially expressed region 10
The base-level coverage is shown in a log2 scale with any overlapping exons shown in dark blue and known introns in light blue.
3.4 plotCluster()
In this example, we noticed with the plotRegionCoverage() plots that most of the candidate DERs are contained in known exons. Sometimes, the signal might be low or we might have used very stringent cutoffs in the derfinder analysis. One way we can observe this is by plotting clusters of regions where a cluster is defined as regions within 300 bp (default option) of each other.
To visualize the clusters, we can use plotCluster() which takes similar input to plotOverview() with the notable addition of the coverage information as well as the idx argument. This argument specifies which region to focus on: it will be plotted with a red bar and will determine the cluster to display.
In Figure 13 we observe one large candidate DER with other nearby ones that do not have a q-value less than 0.10. In a real analysis, we would probably discard this region as the coverage is fairly low.
## First cluster
plotCluster(
idx = 1, regions = regions, annotation = results$annotation,
coverageInfo = fullCov$chr21, txdb = txdb, groupInfo = pheno$group,
titleUse = "pval"
)## Parsing transcripts...## Parsing exons...## Parsing cds...## Parsing utrs...## ------exons...## ------cdss...## ------introns...## ------utr...## aggregating...## Done## Constructing graphics...
Figure 13: Cluster plot for cluster 1 using ggbio
The second cluster (Figure 14) shows a larger number of potential DERs (again without q-values less than 0.10) in a segment of the genome where the coverage data is highly variable. This is a common occurrence with RNA-seq data.
## Second cluster
plotCluster(
idx = 2, regions = regions, annotation = results$annotation,
coverageInfo = fullCov$chr21, txdb = txdb, groupInfo = pheno$group,
titleUse = "pval"
)## Parsing transcripts...## Parsing exons...## Parsing cds...## Parsing utrs...## ------exons...## ------cdss...## ------introns...## ------utr...## aggregating...## Done## Constructing graphics...## Warning in !vapply(ggl, fixed, logical(1L)) & !vapply(PlotList, is, "Ideogram",
## : longer object length is not a multiple of shorter object length## Warning: Transformation introduced infinite values in continuous y-axis
Figure 14: Cluster plot for cluster 2 using ggbio
These plots show an ideogram which helps quickly identify which region of the genome we are focusing on. Then, the base-level coverage information for each sample is displayed in log2. Next, the coverage group means are shown in the log2 scale. The plot is completed with the potential and candidate DERs as well as any known transcripts.
3.5 vennRegions
derfinder has functions for annotating regions given their genomic state. A typical visualization is to then view how many regions overlap known exons, introns, intergenic regions, none of them or several of these groups in a venn diagram. The function vennRegions() makes this plot using the output from derfinder::annotateRegions() as shown in Figure 15.
## Make venn diagram
venn <- vennRegions(annoRegs)
Figure 15: Venn diagram of regions by annotation class
## It returns the actual venn counts information
venn## exon intergenic intron Counts
## 1 0 0 0 0
## 2 0 0 1 2
## 3 0 1 0 4
## 4 0 1 1 0
## 5 1 0 0 259
## 6 1 0 1 35
## 7 1 1 0 0
## 8 1 1 1 0
## attr(,"class")
## [1] "VennCounts"4 Reproducibility
This package was made possible thanks to:
- R (R Core Team, 2023)
- GenomeInfoDb (Arora, Morgan, Carlson, and Pagès, 2017)
- GenomicRanges (Lawrence, Huber, Pagès, Aboyoun, Carlson, Gentleman, Morgan, and Carey, 2013)
- ggbio (Yin, Cook, and Lawrence, 2012)
- ggplot2 (Wickham, 2016)
- IRanges (Lawrence, Huber, Pagès et al., 2013)
- plyr (Wickham, 2011)
- RColorBrewer (Neuwirth, 2022)
- reshape2 (Wickham, 2007)
- scales (Wickham and Seidel, 2022)
- biovizBase (Yin, Lawrence, and Cook, 2023)
- bumphunter (Jaffe, Murakami, Lee, Leek, Fallin, Feinberg, and Irizarry, 2012) and (Jaffe, Murakami, Lee, Leek, Fallin, Feinberg, and Irizarry, 2012)
- derfinder (Collado-Torres, Nellore, Frazee et al., 2017)
- derfinderData (Collado-Torres, Jaffe, and Leek, 2023)
- sessioninfo (Wickham, Chang, Flight, Müller, and Hester, 2021)
- knitr (Xie, 2014)
- BiocStyle (Oleś, 2023)
- RefManageR (McLean, 2017)
- rmarkdown (Allaire, Xie, Dervieux, McPherson, Luraschi, Ushey, Atkins, Wickham, Cheng, Chang, and Iannone, 2023)
- testthat (Wickham, 2011)
- TxDb.Hsapiens.UCSC.hg19.knownGene (Carlson and Maintainer, 2015)
Code for creating the vignette
## Create the vignette
library("rmarkdown")
system.time(render("derfinderPlot.Rmd", "BiocStyle::html_document"))
## Extract the R code
library("knitr")
knit("derfinderPlot.Rmd", tangle = TRUE)## Clean up
unlink("chr21", recursive = TRUE)Date the vignette was generated.
## [1] "2023-10-24 17:00:46 EDT"Wallclock time spent generating the vignette.
## Time difference of 2.001 minsR session information.
## ─ Session info ───────────────────────────────────────────────────────────────────────────────────────────────────────
## setting value
## version R version 4.3.1 (2023-06-16)
## os Ubuntu 22.04.3 LTS
## system x86_64, linux-gnu
## ui X11
## language (EN)
## collate C
## ctype en_US.UTF-8
## tz America/New_York
## date 2023-10-24
## pandoc 2.7.3 @ /usr/bin/ (via rmarkdown)
##
## ─ Packages ───────────────────────────────────────────────────────────────────────────────────────────────────────────
## package * version date (UTC) lib source
## abind 1.4-5 2016-07-21 [2] CRAN (R 4.3.1)
## AnnotationDbi * 1.64.0 2023-10-24 [2] Bioconductor
## AnnotationFilter 1.26.0 2023-10-24 [2] Bioconductor
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## ──────────────────────────────────────────────────────────────────────────────────────────────────────────────────────5 Bibliography
This vignette was generated using BiocStyle (Oleś, 2023) with knitr (Xie, 2014) and rmarkdown (Allaire, Xie, Dervieux et al., 2023) running behind the scenes.
Citations made with RefManageR (McLean, 2017).
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