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This page was generated on 2016-09-02 02:46:03 -0700 (Fri, 02 Sep 2016).
Package 703/1251 | Hostname | OS / Arch | INSTALL | BUILD | CHECK | BUILD BIN | |||||
MEAL 1.3.6 Carlos Ruiz
| zin1 | Linux (Ubuntu 16.04 LTS) / x86_64 | NotNeeded | OK | ERROR | ||||||
moscato1 | Windows Server 2008 R2 Standard (64-bit) / x64 | NotNeeded | OK | [ ERROR ] | OK | ||||||
morelia | Mac OS X Mavericks (10.9.5) / x86_64 | NotNeeded | OK | ERROR | OK |
Package: MEAL |
Version: 1.3.6 |
Command: rm -rf MEAL.buildbin-libdir MEAL.Rcheck && mkdir MEAL.buildbin-libdir MEAL.Rcheck && D:\biocbld\bbs-3.4-bioc\R\bin\R.exe CMD INSTALL --build --merge-multiarch --library=MEAL.buildbin-libdir MEAL_1.3.6.tar.gz >MEAL.Rcheck\00install.out 2>&1 && cp MEAL.Rcheck\00install.out MEAL-install.out && D:\biocbld\bbs-3.4-bioc\R\bin\R.exe CMD check --library=MEAL.buildbin-libdir --install="check:MEAL-install.out" --force-multiarch --no-vignettes --timings MEAL_1.3.6.tar.gz |
StartedAt: 2016-09-01 13:54:16 -0700 (Thu, 01 Sep 2016) |
EndedAt: 2016-09-01 14:10:44 -0700 (Thu, 01 Sep 2016) |
EllapsedTime: 987.9 seconds |
RetCode: 1 |
Status: ERROR |
CheckDir: MEAL.Rcheck |
Warnings: NA |
############################################################################## ############################################################################## ### ### Running command: ### ### rm -rf MEAL.buildbin-libdir MEAL.Rcheck && mkdir MEAL.buildbin-libdir MEAL.Rcheck && D:\biocbld\bbs-3.4-bioc\R\bin\R.exe CMD INSTALL --build --merge-multiarch --library=MEAL.buildbin-libdir MEAL_1.3.6.tar.gz >MEAL.Rcheck\00install.out 2>&1 && cp MEAL.Rcheck\00install.out MEAL-install.out && D:\biocbld\bbs-3.4-bioc\R\bin\R.exe CMD check --library=MEAL.buildbin-libdir --install="check:MEAL-install.out" --force-multiarch --no-vignettes --timings MEAL_1.3.6.tar.gz ### ############################################################################## ############################################################################## * using log directory 'D:/biocbld/bbs-3.4-bioc/meat/MEAL.Rcheck' * using R version 3.3.1 (2016-06-21) * using platform: x86_64-w64-mingw32 (64-bit) * using session charset: ISO8859-1 * using option '--no-vignettes' * checking for file 'MEAL/DESCRIPTION' ... OK * this is package 'MEAL' version '1.3.6' * checking package namespace information ... OK * checking package dependencies ... OK * checking if this is a source package ... OK * checking if there is a namespace ... OK * checking for hidden files and directories ... OK * checking for portable file names ... OK * checking whether package 'MEAL' can be installed ... OK * checking installed package size ... OK * checking package directory ... OK * checking 'build' directory ... OK * checking DESCRIPTION meta-information ... OK * checking top-level files ... OK * checking for left-over files ... OK * checking index information ... OK * checking package subdirectories ... OK * checking R files for non-ASCII characters ... OK * checking R files for syntax errors ... OK * loading checks for arch 'i386' ** checking whether the package can be loaded ... OK ** checking whether the package can be loaded with stated dependencies ... OK ** checking whether the package can be unloaded cleanly ... OK ** checking whether the namespace can be loaded with stated dependencies ... OK ** checking whether the namespace can be unloaded cleanly ... OK ** checking loading without being on the library search path ... OK * loading checks for arch 'x64' ** checking whether the package can be loaded ... OK ** checking whether the package can be loaded with stated dependencies ... OK ** checking whether the package can be unloaded cleanly ... OK ** checking whether the namespace can be loaded with stated dependencies ... OK ** checking whether the namespace can be unloaded cleanly ... OK ** checking loading without being on the library search path ... OK * checking dependencies in R code ... OK * checking S3 generic/method consistency ... OK * checking replacement functions ... OK * checking foreign function calls ... OK * checking R code for possible problems ... NOTE DARegion : <anonymous>: no visible binding for global variable 'proberes' correlationMethExprs: no visible global function definition for 'rowRanges' Undefined global functions or variables: proberes rowRanges * checking Rd files ... OK * checking Rd metadata ... OK * checking Rd cross-references ... OK * checking for missing documentation entries ... OK * checking for code/documentation mismatches ... WARNING Codoc mismatches from documentation object 'DARegion': DARegion Code: function(set, model, methods = c("blockFinder", "bumphunter", "DMRcate"), coefficient = 2, num_permutations = 0, bumphunter_cutoff = 0.05, bumps_max = 30000, num_cores = 1, verbose = FALSE, ...) Docs: function(set, model, proberes, methods = c("blockFinder", "bumphunter", "DMRcate"), coefficient = 2, num_permutations = 0, bumphunter_cutoff = 0.05, bumps_max = 30000, num_cores = 1, verbose = FALSE, ...) Argument names in docs not in code: proberes Mismatches in argument names (first 3): Position: 3 Code: methods Docs: proberes Position: 4 Code: coefficient Docs: methods Position: 5 Code: num_permutations Docs: coefficient * checking Rd \usage sections ... OK * checking Rd contents ... OK * checking for unstated dependencies in examples ... OK * checking installed files from 'inst/doc' ... OK * checking files in 'vignettes' ... OK * checking examples ... ** running examples for arch 'i386' ... OK Examples with CPU or elapsed time > 5s user system elapsed plotRegion-methods 50.50 0.36 50.85 topRDAhits-methods 46.41 0.36 46.77 plotRDA-methods 45.92 0.28 46.21 DAPipeline 19.67 0.56 22.42 ** running examples for arch 'x64' ... OK Examples with CPU or elapsed time > 5s user system elapsed topRDAhits-methods 51.40 0.55 52.01 plotRegion-methods 51.53 0.40 51.98 plotRDA-methods 51.49 0.41 51.93 DAPipeline 19.38 0.59 20.70 * checking for unstated dependencies in 'tests' ... OK * checking tests ... ** running tests for arch 'i386' ... Running 'testthat.R' Warning message: running command '"D:/biocbld/BBS-3˜1.4-B/R/bin/i386/R" CMD BATCH --vanilla "testthat.R" "testthat.Rout"' had status 1 ERROR Running the tests in 'tests/testthat.R' failed. Last 13 lines of output: 2: In add_eset(object, methySet, dataset.type = "methylation", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 3: In add_eset(object, snpSet, dataset.type = "snps", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 4: In add_eset(object, methySet, dataset.type = "methylation", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 5: In add_eset(object, snpSet, dataset.type = "snps", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 6: In add_eset(object, gexpSet, dataset.type = "expression", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 7: In add_eset(object, methySet, dataset.type = "methylation", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames Execution halted ** running tests for arch 'x64' ... Running 'testthat.R' Warning message: running command '"D:/biocbld/BBS-3˜1.4-B/R/bin/x64/R" CMD BATCH --vanilla "testthat.R" "testthat.Rout"' had status 1 ERROR Running the tests in 'tests/testthat.R' failed. Last 13 lines of output: 2: In add_eset(object, methySet, dataset.type = "methylation", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 3: In add_eset(object, snpSet, dataset.type = "snps", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 4: In add_eset(object, methySet, dataset.type = "methylation", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 5: In add_eset(object, snpSet, dataset.type = "snps", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 6: In add_eset(object, gexpSet, dataset.type = "expression", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 7: In add_eset(object, methySet, dataset.type = "methylation", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames Execution halted * checking for unstated dependencies in vignettes ... OK * checking package vignettes in 'inst/doc' ... OK * checking running R code from vignettes ... SKIPPED * checking re-building of vignette outputs ... SKIPPED * checking PDF version of manual ... OK * DONE Status: 2 ERRORs, 1 WARNING, 1 NOTE See 'D:/biocbld/bbs-3.4-bioc/meat/MEAL.Rcheck/00check.log' for details.
testthat.Rout.fail:
R version 3.3.1 (2016-06-21) -- "Bug in Your Hair" Copyright (C) 2016 The R Foundation for Statistical Computing Platform: i386-w64-mingw32/i386 (32-bit) R is free software and comes with ABSOLUTELY NO WARRANTY. You are welcome to redistribute it under certain conditions. Type 'license()' or 'licence()' for distribution details. R is a collaborative project with many contributors. Type 'contributors()' for more information and 'citation()' on how to cite R or R packages in publications. Type 'demo()' for some demos, 'help()' for on-line help, or 'help.start()' for an HTML browser interface to help. Type 'q()' to quit R. > library(testthat) > library(MEAL) Loading required package: Biobase Loading required package: BiocGenerics Loading required package: parallel Attaching package: 'BiocGenerics' The following objects are masked from 'package:parallel': clusterApply, clusterApplyLB, clusterCall, clusterEvalQ, clusterExport, clusterMap, parApply, parCapply, parLapply, parLapplyLB, parRapply, parSapply, parSapplyLB The following objects are masked from 'package:stats': IQR, mad, xtabs The following objects are masked from 'package:base': Filter, Find, Map, Position, Reduce, anyDuplicated, append, as.data.frame, cbind, colnames, do.call, duplicated, eval, evalq, get, grep, grepl, intersect, is.unsorted, lapply, lengths, mapply, match, mget, order, paste, pmax, pmax.int, pmin, pmin.int, rank, rbind, rownames, sapply, setdiff, sort, table, tapply, union, unique, unsplit, which, which.max, which.min Welcome to Bioconductor Vignettes contain introductory material; view with 'browseVignettes()'. To cite Bioconductor, see 'citation("Biobase")', and for packages 'citation("pkgname")'. Loading required package: MultiDataSet Setting options('download.file.method.GEOquery'='auto') Setting options('GEOquery.inmemory.gpl'=FALSE) > > test_check("MEAL") Loading required package: minfi Loading required package: lattice Loading required package: GenomicRanges Loading required package: stats4 Loading required package: S4Vectors Attaching package: 'S4Vectors' The following object is masked from 'package:testthat': compare The following objects are masked from 'package:base': colMeans, colSums, expand.grid, rowMeans, rowSums Loading required package: IRanges Loading required package: GenomeInfoDb Loading required package: SummarizedExperiment Loading required package: Biostrings Loading required package: XVector Loading required package: bumphunter Loading required package: foreach Loading required package: iterators Loading required package: locfit locfit 1.5-9.1 2013-03-22 Loading required package: IlluminaHumanMethylation450kmanifest Loading required package: IlluminaHumanMethylation450kanno.ilmn12.hg19 Your contrast returned 82 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrX... Fitting chrY... Demarcating regions... Done! 1. Failure: Check Errors (@test_06regionAnalysis.R#70) ------------------------- error$message does not match "set must be a MethylationSet.". Actual value: "The number of samples is different in the set and in the model." 2. Failure: Check Errors (@test_06regionAnalysis.R#71) ------------------------- error$message does not match "The set is empty.". Actual value: "object 'emptyset' not found" coercing object of mode numeric to SnpMatrix Number of significant surrogate variables is: 1 Iteration (out of 5 ):1 2 3 4 5 Your contrast returned 10 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! Your contrast returned no individually significant probes. Set pcutoff manually in dmrcate() to return DMRs, but be warned there is an increased risk of Type I errors. Fitting chrY... Your contrast returned 10 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! Your contrast returned 10 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! Your contrast returned no individually significant probes. Set pcutoff manually in dmrcate() to return DMRs, but be warned there is an increased risk of Type I errors. Fitting chrY... Your contrast returned 10 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! Your contrast returned 5 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! 'nperm' >= set of all permutations: complete enumeration. Set of permutations < 'minperm'. Generating entire set. coercing object of mode numeric to SnpMatrix Your contrast returned 5 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! 'nperm' >= set of all permutations: complete enumeration. Set of permutations < 'minperm'. Generating entire set. Your contrast returned 5 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! Your contrast returned 5 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! coercing object of mode numeric to SnpMatrix Your contrast returned 10 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! Your contrast returned no individually significant probes. Set pcutoff manually in dmrcate() to return DMRs, but be warned there is an increased risk of Type I errors. Fitting chrY... Your contrast returned 10 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! testthat results ================================================================ OK: 240 SKIPPED: 0 FAILED: 2 1. Failure: Check Errors (@test_06regionAnalysis.R#70) 2. Failure: Check Errors (@test_06regionAnalysis.R#71) Error: testthat unit tests failed In addition: Warning messages: 1: In matrix(runif(6, max = 15), 4) : data length [6] is not a sub-multiple or multiple of the number of rows [4] 2: In add_eset(object, methySet, dataset.type = "methylation", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 3: In add_eset(object, snpSet, dataset.type = "snps", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 4: In add_eset(object, methySet, dataset.type = "methylation", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 5: In add_eset(object, snpSet, dataset.type = "snps", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 6: In add_eset(object, gexpSet, dataset.type = "expression", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 7: In add_eset(object, methySet, dataset.type = "methylation", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames Execution halted
testthat.Rout.fail:
R version 3.3.1 (2016-06-21) -- "Bug in Your Hair" Copyright (C) 2016 The R Foundation for Statistical Computing Platform: x86_64-w64-mingw32/x64 (64-bit) R is free software and comes with ABSOLUTELY NO WARRANTY. You are welcome to redistribute it under certain conditions. Type 'license()' or 'licence()' for distribution details. R is a collaborative project with many contributors. Type 'contributors()' for more information and 'citation()' on how to cite R or R packages in publications. Type 'demo()' for some demos, 'help()' for on-line help, or 'help.start()' for an HTML browser interface to help. Type 'q()' to quit R. > library(testthat) > library(MEAL) Loading required package: Biobase Loading required package: BiocGenerics Loading required package: parallel Attaching package: 'BiocGenerics' The following objects are masked from 'package:parallel': clusterApply, clusterApplyLB, clusterCall, clusterEvalQ, clusterExport, clusterMap, parApply, parCapply, parLapply, parLapplyLB, parRapply, parSapply, parSapplyLB The following objects are masked from 'package:stats': IQR, mad, xtabs The following objects are masked from 'package:base': Filter, Find, Map, Position, Reduce, anyDuplicated, append, as.data.frame, cbind, colnames, do.call, duplicated, eval, evalq, get, grep, grepl, intersect, is.unsorted, lapply, lengths, mapply, match, mget, order, paste, pmax, pmax.int, pmin, pmin.int, rank, rbind, rownames, sapply, setdiff, sort, table, tapply, union, unique, unsplit, which, which.max, which.min Welcome to Bioconductor Vignettes contain introductory material; view with 'browseVignettes()'. To cite Bioconductor, see 'citation("Biobase")', and for packages 'citation("pkgname")'. Loading required package: MultiDataSet Setting options('download.file.method.GEOquery'='auto') Setting options('GEOquery.inmemory.gpl'=FALSE) > > test_check("MEAL") Loading required package: minfi Loading required package: lattice Loading required package: GenomicRanges Loading required package: stats4 Loading required package: S4Vectors Attaching package: 'S4Vectors' The following object is masked from 'package:testthat': compare The following objects are masked from 'package:base': colMeans, colSums, expand.grid, rowMeans, rowSums Loading required package: IRanges Loading required package: GenomeInfoDb Loading required package: SummarizedExperiment Loading required package: Biostrings Loading required package: XVector Loading required package: bumphunter Loading required package: foreach Loading required package: iterators Loading required package: locfit locfit 1.5-9.1 2013-03-22 Loading required package: IlluminaHumanMethylation450kmanifest Loading required package: IlluminaHumanMethylation450kanno.ilmn12.hg19 Your contrast returned 82 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrX... Fitting chrY... Demarcating regions... Done! 1. Failure: Check Errors (@test_06regionAnalysis.R#70) ------------------------- error$message does not match "set must be a MethylationSet.". Actual value: "The number of samples is different in the set and in the model." 2. Failure: Check Errors (@test_06regionAnalysis.R#71) ------------------------- error$message does not match "The set is empty.". Actual value: "object 'emptyset' not found" Number of significant surrogate variables is: 1 Iteration (out of 5 ):1 2 3 4 5 coercing object of mode numeric to SnpMatrix Your contrast returned 10 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! Your contrast returned no individually significant probes. Set pcutoff manually in dmrcate() to return DMRs, but be warned there is an increased risk of Type I errors. Fitting chrY... Your contrast returned 10 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! Your contrast returned 10 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! Your contrast returned no individually significant probes. Set pcutoff manually in dmrcate() to return DMRs, but be warned there is an increased risk of Type I errors. Fitting chrY... Your contrast returned 10 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! Your contrast returned 5 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! 'nperm' >= set of all permutations: complete enumeration. Set of permutations < 'minperm'. Generating entire set. coercing object of mode numeric to SnpMatrix Your contrast returned 5 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! 'nperm' >= set of all permutations: complete enumeration. Set of permutations < 'minperm'. Generating entire set. Your contrast returned 5 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! Your contrast returned 5 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! coercing object of mode numeric to SnpMatrix Your contrast returned 10 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! Your contrast returned no individually significant probes. Set pcutoff manually in dmrcate() to return DMRs, but be warned there is an increased risk of Type I errors. Fitting chrY... Your contrast returned 10 individually significant probes; a small but real effect. Consider manually setting the value of pcutoff to return more DMRs, but be warned that doing this increases the risk of Type I errors. Fitting chrY... Demarcating regions... Done! testthat results ================================================================ OK: 240 SKIPPED: 0 FAILED: 2 1. Failure: Check Errors (@test_06regionAnalysis.R#70) 2. Failure: Check Errors (@test_06regionAnalysis.R#71) Error: testthat unit tests failed In addition: Warning messages: 1: In matrix(runif(6, max = 15), 4) : data length [6] is not a sub-multiple or multiple of the number of rows [4] 2: In add_eset(object, methySet, dataset.type = "methylation", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 3: In add_eset(object, snpSet, dataset.type = "snps", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 4: In add_eset(object, methySet, dataset.type = "methylation", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 5: In add_eset(object, snpSet, dataset.type = "snps", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 6: In add_eset(object, gexpSet, dataset.type = "expression", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames 7: In add_eset(object, methySet, dataset.type = "methylation", GRanges = range, : No id column found in pData. The id will be equal to the sampleNames Execution halted
MEAL.Rcheck/00install.out:
install for i386 * installing *source* package 'MEAL' ... ** R ** inst ** preparing package for lazy loading ** help *** installing help indices ** building package indices ** installing vignettes ** testing if installed package can be loaded install for x64 * installing *source* package 'MEAL' ... ** testing if installed package can be loaded * MD5 sums packaged installation of 'MEAL' as MEAL_1.3.6.zip * DONE (MEAL)
MEAL.Rcheck/examples_i386/MEAL-Ex.timings:
name | user | system | elapsed | |
AnalysisRegionResults-class | 0 | 0 | 0 | |
AnalysisResults-class | 0 | 0 | 0 | |
DAPipeline | 19.67 | 0.56 | 22.42 | |
DAProbe | 0.56 | 0.01 | 0.57 | |
DARegion | 2.13 | 0.10 | 2.23 | |
DARegionAnalysis | 2.87 | 0.18 | 3.14 | |
RDAset | 1.92 | 0.21 | 2.12 | |
calculateRelevantSNPs | 0.01 | 0.00 | 0.02 | |
createRanges | 0.02 | 0.00 | 0.01 | |
explainedVariance | 0.03 | 0.00 | 0.04 | |
exportResults-methods | 1.98 | 0.11 | 2.10 | |
filterSet-methods | 1.71 | 0.03 | 1.74 | |
getGeneVals-methods | 2.07 | 0.04 | 2.12 | |
multiCorrMethExprs | 0 | 0 | 0 | |
normalSNP | 0 | 0 | 0 | |
plotBestFeatures | 2.30 | 0.05 | 2.34 | |
plotEWAS-methods | 2.44 | 0.03 | 2.47 | |
plotFeature | 2.02 | 0.04 | 2.07 | |
plotLM | 0.21 | 0.00 | 0.21 | |
plotQQ-methods | 2.45 | 0.08 | 2.53 | |
plotRDA-methods | 45.92 | 0.28 | 46.21 | |
plotRegion-methods | 50.50 | 0.36 | 50.85 | |
plotVolcano-methods | 2.67 | 0.11 | 2.78 | |
preparePhenotype | 0 | 0 | 0 | |
topRDAhits-methods | 46.41 | 0.36 | 46.77 | |
MEAL.Rcheck/examples_x64/MEAL-Ex.timings:
name | user | system | elapsed | |
AnalysisRegionResults-class | 0 | 0 | 0 | |
AnalysisResults-class | 0 | 0 | 0 | |
DAPipeline | 19.38 | 0.59 | 20.70 | |
DAProbe | 0.51 | 0.03 | 0.55 | |
DARegion | 2.76 | 0.08 | 2.84 | |
DARegionAnalysis | 3.39 | 0.15 | 3.54 | |
RDAset | 2.40 | 0.02 | 2.41 | |
calculateRelevantSNPs | 0 | 0 | 0 | |
createRanges | 0.01 | 0.00 | 0.02 | |
explainedVariance | 0.05 | 0.00 | 0.04 | |
exportResults-methods | 2.34 | 0.03 | 2.37 | |
filterSet-methods | 1.95 | 0.05 | 2.02 | |
getGeneVals-methods | 2.28 | 0.04 | 2.32 | |
multiCorrMethExprs | 0 | 0 | 0 | |
normalSNP | 0 | 0 | 0 | |
plotBestFeatures | 2.38 | 0.08 | 2.44 | |
plotEWAS-methods | 2.79 | 0.14 | 3.53 | |
plotFeature | 2.39 | 0.08 | 2.47 | |
plotLM | 0.23 | 0.00 | 0.23 | |
plotQQ-methods | 2.78 | 0.11 | 2.89 | |
plotRDA-methods | 51.49 | 0.41 | 51.93 | |
plotRegion-methods | 51.53 | 0.40 | 51.98 | |
plotVolcano-methods | 3.25 | 0.11 | 3.35 | |
preparePhenotype | 0 | 0 | 0 | |
topRDAhits-methods | 51.40 | 0.55 | 52.01 | |