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ABCD[E]FGHIJKLMNOPQRSTUVWXYZ

CHECK report for easyRNASeq on tokay2

This page was generated on 2020-10-17 11:56:30 -0400 (Sat, 17 Oct 2020).

TO THE DEVELOPERS/MAINTAINERS OF THE easyRNASeq PACKAGE: Please make sure to use the following settings in order to reproduce any error or warning you see on this page.
Package 518/1905HostnameOS / ArchINSTALLBUILDCHECKBUILD BIN
easyRNASeq 2.24.1
Nicolas Delhomme
Snapshot Date: 2020-10-16 14:40:19 -0400 (Fri, 16 Oct 2020)
URL: https://git.bioconductor.org/packages/easyRNASeq
Branch: RELEASE_3_11
Last Commit: df859ff
Last Changed Date: 2020-04-27 18:15:51 -0400 (Mon, 27 Apr 2020)
malbec2 Linux (Ubuntu 18.04.4 LTS) / x86_64  OK  OK  OK UNNEEDED, same version exists in internal repository
tokay2 Windows Server 2012 R2 Standard / x64  OK  OK [ OK ] OK UNNEEDED, same version exists in internal repository
machv2 macOS 10.14.6 Mojave / x86_64  OK  OK  OK  OK UNNEEDED, same version exists in internal repository

Summary

Package: easyRNASeq
Version: 2.24.1
Command: C:\Users\biocbuild\bbs-3.11-bioc\R\bin\R.exe CMD check --force-multiarch --install=check:easyRNASeq.install-out.txt --library=C:\Users\biocbuild\bbs-3.11-bioc\R\library --no-vignettes --timings easyRNASeq_2.24.1.tar.gz
StartedAt: 2020-10-17 03:37:17 -0400 (Sat, 17 Oct 2020)
EndedAt: 2020-10-17 04:03:32 -0400 (Sat, 17 Oct 2020)
EllapsedTime: 1574.2 seconds
RetCode: 0
Status:  OK  
CheckDir: easyRNASeq.Rcheck
Warnings: 0

Command output

##############################################################################
##############################################################################
###
### Running command:
###
###   C:\Users\biocbuild\bbs-3.11-bioc\R\bin\R.exe CMD check --force-multiarch --install=check:easyRNASeq.install-out.txt --library=C:\Users\biocbuild\bbs-3.11-bioc\R\library --no-vignettes --timings easyRNASeq_2.24.1.tar.gz
###
##############################################################################
##############################################################################


* using log directory 'C:/Users/biocbuild/bbs-3.11-bioc/meat/easyRNASeq.Rcheck'
* using R version 4.0.3 (2020-10-10)
* using platform: x86_64-w64-mingw32 (64-bit)
* using session charset: ISO8859-1
* using option '--no-vignettes'
* checking for file 'easyRNASeq/DESCRIPTION' ... OK
* checking extension type ... Package
* this is package 'easyRNASeq' version '2.24.1'
* package encoding: UTF-8
* checking package namespace information ... OK
* checking package dependencies ... NOTE
Files named as vignettes but with no recognized vignette engine:
   'inst/doc/01-Introduction.Rmd'
   'inst/doc/02-AnnotParam.Rmd'
   'inst/doc/03-SyntheticTranscripts.Rmd'
   'inst/doc/04-BamParam.Rmd'
   'inst/doc/05-RnaSeqParam.Rmd'
   'inst/doc/06-simpleRNASeq.Rmd'
   'inst/doc/07-cleanUp.Rmd'
   'inst/doc/08-Session-Info.Rmd'
   'inst/doc/09-Acknowledgments.Rmd'
   'inst/doc/10-Foonotes.Rmd'
   'inst/doc/11-Images.Rmd'
   'inst/doc/12-Appendix.Rmd'
(Is a VignetteBuilder field missing?)
* 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 'easyRNASeq' 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
* 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 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 ... OK
* checking Rd files ... OK
* checking Rd metadata ... OK
* checking Rd cross-references ... OK
* checking for missing documentation entries ... OK
* checking for code/documentation mismatches ... OK
* checking Rd \usage sections ... OK
* checking Rd contents ... OK
* checking for unstated dependencies in examples ... OK
* checking contents of 'data' directory ... OK
* checking data for non-ASCII characters ... OK
* checking data for ASCII and uncompressed saves ... OK
* checking line endings in Makefiles ... OK
* checking for GNU extensions in Makefiles ... OK
* checking include directives in Makefiles ... OK
* checking files in 'vignettes' ... OK
* checking examples ...
** running examples for arch 'i386' ... OK
Examples with CPU (user + system) or elapsed time > 5s
                                   user system elapsed
easyRNASeq-simpleRNASeq          123.66   0.84  128.94
easyRNASeq-package                61.14   3.56   68.45
easyRNASeq-synthetic-transcripts  43.75   0.08   44.41
BiocFileCache-methods             21.79   1.23   37.83
easyRNASeq-BamFileList            14.92   0.71   53.44
Rsamtools-methods                 12.11   0.51   14.75
** running examples for arch 'x64' ... OK
Examples with CPU (user + system) or elapsed time > 5s
                                   user system elapsed
easyRNASeq-simpleRNASeq          108.18   0.90  111.06
easyRNASeq-package                55.39   1.21   59.93
easyRNASeq-synthetic-transcripts  37.88   0.03   38.62
BiocFileCache-methods             22.14   1.06  117.42
easyRNASeq-BamFileList            15.16   0.53   90.11
Rsamtools-methods                 11.56   0.51   13.89
* checking for unstated dependencies in 'tests' ... OK
* checking tests ...
** running tests for arch 'i386' ...
  Running 'runTests.R'
 OK
** running tests for arch 'x64' ...
  Running 'runTests.R'
 OK
* 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: 1 NOTE
See
  'C:/Users/biocbuild/bbs-3.11-bioc/meat/easyRNASeq.Rcheck/00check.log'
for details.



Installation output

easyRNASeq.Rcheck/00install.out

##############################################################################
##############################################################################
###
### Running command:
###
###   C:\cygwin\bin\curl.exe -O https://malbec2.bioconductor.org/BBS/3.11/bioc/src/contrib/easyRNASeq_2.24.1.tar.gz && rm -rf easyRNASeq.buildbin-libdir && mkdir easyRNASeq.buildbin-libdir && C:\Users\biocbuild\bbs-3.11-bioc\R\bin\R.exe CMD INSTALL --merge-multiarch --build --library=easyRNASeq.buildbin-libdir easyRNASeq_2.24.1.tar.gz && C:\Users\biocbuild\bbs-3.11-bioc\R\bin\R.exe CMD INSTALL easyRNASeq_2.24.1.zip && rm easyRNASeq_2.24.1.tar.gz easyRNASeq_2.24.1.zip
###
##############################################################################
##############################################################################


  % Total    % Received % Xferd  Average Speed   Time    Time     Time  Current
                                 Dload  Upload   Total   Spent    Left  Speed

  0     0    0     0    0     0      0      0 --:--:-- --:--:-- --:--:--     0
  0  123k    0     0    0     0      0      0 --:--:-- --:--:-- --:--:--     0
100  123k  100  123k    0     0  1945k      0 --:--:-- --:--:-- --:--:-- 2134k

install for i386

* installing *source* package 'easyRNASeq' ...
** using staged installation
** R
** data
** inst
** byte-compile and prepare package for lazy loading
Creating a generic function for 'basename' from package 'base' in package 'easyRNASeq'
Creating a generic function for 'file.exists' from package 'base' in package 'easyRNASeq'
** help
*** installing help indices
  converting help for package 'easyRNASeq'
    finding HTML links ... done
    BiocFileCache-methods                   html  
    finding level-2 HTML links ... done

    DESeq-methods                           html  
    GenomicRanges-methods                   html  
    IRanges-methods                         html  
    Rsamtools-methods                       html  
    ShortRead-methods                       html  
    basename-methods                        html  
    easyRNASeq-AnnotParam-accessors         html  
    easyRNASeq-AnnotParam-class             html  
    easyRNASeq-AnnotParam                   html  
    easyRNASeq-BamFileList                  html  
    easyRNASeq-BamParam-accessors           html  
    easyRNASeq-BamParam-class               html  
    easyRNASeq-BamParam                     html  
    easyRNASeq-RnaSeqParam-accessors        html  
    easyRNASeq-RnaSeqParam-class            html  
    easyRNASeq-RnaSeqParam                  html  
    easyRNASeq-accessors                    html  
    easyRNASeq-annotation-internal-methods
                                            html  
    easyRNASeq-annotation-methods           html  
    easyRNASeq-class                        html  
    easyRNASeq-correction-methods           html  
    easyRNASeq-coverage-methods             html  
    easyRNASeq-datasets                     html  
    easyRNASeq-defunct-annotation-methods   html  
    easyRNASeq-defunct                      html  
    easyRNASeq-easyRNASeq                   html  
    easyRNASeq-global-variables             html  
    easyRNASeq-internal-AnnotParam-methods
                                            html  
    easyRNASeq-internal-methods             html  
    easyRNASeq-island-methods               html  
    easyRNASeq-package                      html  
    easyRNASeq-simpleRNASeq                 html  
    easyRNASeq-summarization-internal-methods
                                            html  
    easyRNASeq-summarization-methods        html  
    easyRNASeq-synthetic-transcripts        html  
    edgeR-methods                           html  
    file.exists-methods                     html  
    genomeIntervals-methods                 html  
    parallel-methods                        html  
    print-methods                           html  
    show-methods                            html  
** building package indices
** installing vignettes
** testing if installed package can be loaded from temporary location
** testing if installed package can be loaded from final location
** testing if installed package keeps a record of temporary installation path

install for x64

* installing *source* package 'easyRNASeq' ...
** testing if installed package can be loaded
* MD5 sums
packaged installation of 'easyRNASeq' as easyRNASeq_2.24.1.zip
* DONE (easyRNASeq)
* installing to library 'C:/Users/biocbuild/bbs-3.11-bioc/R/library'
package 'easyRNASeq' successfully unpacked and MD5 sums checked

Tests output

easyRNASeq.Rcheck/tests_i386/runTests.Rout


R version 4.0.3 (2020-10-10) -- "Bunny-Wunnies Freak Out"
Copyright (C) 2020 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.

> # get the example data
> library(easyRNASeq)
> tutorialData()
[1] "C:/Users/biocbuild/AppData/Local/easyRNASeq/easyRNASeq/Cache"
> 
> # set the env.var
> #TUTORIAL.DATA <- get("TUTORIAL.DATA",envir=as.environment("package:easyRNASeq"))
> 
> # run the tests
> BiocGenerics:::testPackage("easyRNASeq")
Loading required package: GenomicRanges
Loading required package: stats4
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 object is masked from 'package:easyRNASeq':

    basename

The following objects are masked from 'package:stats':

    IQR, mad, sd, var, xtabs

The following objects are masked from 'package:base':

    Filter, Find, Map, Position, Reduce, anyDuplicated, append,
    as.data.frame, basename, cbind, colnames, dirname, do.call,
    duplicated, eval, evalq, get, grep, grepl, intersect, is.unsorted,
    lapply, 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

Loading required package: S4Vectors

Attaching package: 'S4Vectors'

The following object is masked from 'package:base':

    expand.grid

Loading required package: IRanges

Attaching package: 'IRanges'

The following object is masked from 'package:grDevices':

    windows

Loading required package: GenomeInfoDb
No validation performed at that stage
Validated a datasource of type biomaRt
No validation performed at that stage
Validated a datasource of type rda
Read 1000 records
Validated a datasource of type gtf
Read 999 records
Validated a datasource of type gff3


RUNIT TEST PROTOCOL -- Sat Oct 17 04:00:59 2020 
*********************************************** 
Number of test functions: 20 
Number of errors: 0 
Number of failures: 0 

 
1 Test Suite : 
easyRNASeq RUnit Tests - 20 test functions, 0 errors, 0 failures
Number of test functions: 20 
Number of errors: 0 
Number of failures: 0 
Warning messages:
1: In FUN(X[[i]], ...) :
  Bam file: 3370163c2e86_ACTAGC.bam is considered unstranded.
2: In FUN(X[[i]], ...) :
  Bam file: 3370163c2e86_ACTAGC.bam Strandedness could not be determined using 14772 regions spanning 1023473 bp on either strand at a 90% cutoff; 76.6 percent appear to be stranded.
3: In FUN(X[[i]], ...) :
  Bam file: 337023e76e0f_ACACTG.bam is considered unstranded.
4: In FUN(X[[i]], ...) :
  Bam file: 337023e76e0f_ACACTG.bam Strandedness could not be determined using 18615 regions spanning 1300192 bp on either strand at a 90% cutoff; 73.67 percent appear to be stranded.
5: In FUN(X[[i]], ...) :
  Bam file: 33706f1b3731_ATGGCT.bam is considered unstranded.
6: In FUN(X[[i]], ...) :
  Bam file: 33706f1b3731_ATGGCT.bam Strandedness could not be determined using 18462 regions spanning 1280337 bp on either strand at a 90% cutoff; 74.26 percent appear to be stranded.
7: In FUN(X[[i]], ...) :
  Bam file: 3370c9c2c8c_TTGCGA.bam is considered unstranded.
8: In FUN(X[[i]], ...) :
  Bam file: 3370c9c2c8c_TTGCGA.bam Strandedness could not be determined using 19659 regions spanning 1381886 bp on either strand at a 90% cutoff; 73.37 percent appear to be stranded.
9: In simpleRNASeq(bamFiles = bamFiles, param = param, verbose = FALSE) :
  As of version 2.15.5, easyRNASeq assumes that, if the data is strand specific, the sequencing was done using a protocol such as the Illumina TruSeq, where the reverse strand is quantified - i.e. the strandProtocol argument of the BamParam class defaults to 'reverse'.
> 
> # cleanup
> # removebfc(easyRNASeq:::.get_cache(),ask=FALSE)
> 
> proc.time()
   user  system elapsed 
 114.73    4.09  143.84 

easyRNASeq.Rcheck/tests_x64/runTests.Rout


R version 4.0.3 (2020-10-10) -- "Bunny-Wunnies Freak Out"
Copyright (C) 2020 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.

> # get the example data
> library(easyRNASeq)
> tutorialData()
[1] "C:/Users/biocbuild/AppData/Local/easyRNASeq/easyRNASeq/Cache"
> 
> # set the env.var
> #TUTORIAL.DATA <- get("TUTORIAL.DATA",envir=as.environment("package:easyRNASeq"))
> 
> # run the tests
> BiocGenerics:::testPackage("easyRNASeq")
Loading required package: GenomicRanges
Loading required package: stats4
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 object is masked from 'package:easyRNASeq':

    basename

The following objects are masked from 'package:stats':

    IQR, mad, sd, var, xtabs

The following objects are masked from 'package:base':

    Filter, Find, Map, Position, Reduce, anyDuplicated, append,
    as.data.frame, basename, cbind, colnames, dirname, do.call,
    duplicated, eval, evalq, get, grep, grepl, intersect, is.unsorted,
    lapply, 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

Loading required package: S4Vectors

Attaching package: 'S4Vectors'

The following object is masked from 'package:base':

    expand.grid

Loading required package: IRanges

Attaching package: 'IRanges'

The following object is masked from 'package:grDevices':

    windows

Loading required package: GenomeInfoDb
No validation performed at that stage
Validated a datasource of type biomaRt
No validation performed at that stage
Validated a datasource of type rda
Read 1000 records
Validated a datasource of type gtf
Read 999 records
Validated a datasource of type gff3


RUNIT TEST PROTOCOL -- Sat Oct 17 04:03:17 2020 
*********************************************** 
Number of test functions: 20 
Number of errors: 0 
Number of failures: 0 

 
1 Test Suite : 
easyRNASeq RUnit Tests - 20 test functions, 0 errors, 0 failures
Number of test functions: 20 
Number of errors: 0 
Number of failures: 0 
Warning messages:
1: In FUN(X[[i]], ...) :
  Bam file: 3370163c2e86_ACTAGC.bam is considered unstranded.
2: In FUN(X[[i]], ...) :
  Bam file: 3370163c2e86_ACTAGC.bam Strandedness could not be determined using 14772 regions spanning 1023473 bp on either strand at a 90% cutoff; 76.6 percent appear to be stranded.
3: In FUN(X[[i]], ...) :
  Bam file: 337023e76e0f_ACACTG.bam is considered unstranded.
4: In FUN(X[[i]], ...) :
  Bam file: 337023e76e0f_ACACTG.bam Strandedness could not be determined using 18615 regions spanning 1300192 bp on either strand at a 90% cutoff; 73.67 percent appear to be stranded.
5: In FUN(X[[i]], ...) :
  Bam file: 33706f1b3731_ATGGCT.bam is considered unstranded.
6: In FUN(X[[i]], ...) :
  Bam file: 33706f1b3731_ATGGCT.bam Strandedness could not be determined using 18462 regions spanning 1280337 bp on either strand at a 90% cutoff; 74.26 percent appear to be stranded.
7: In FUN(X[[i]], ...) :
  Bam file: 3370c9c2c8c_TTGCGA.bam is considered unstranded.
8: In FUN(X[[i]], ...) :
  Bam file: 3370c9c2c8c_TTGCGA.bam Strandedness could not be determined using 19659 regions spanning 1381886 bp on either strand at a 90% cutoff; 73.37 percent appear to be stranded.
9: In simpleRNASeq(bamFiles = bamFiles, param = param, verbose = FALSE) :
  As of version 2.15.5, easyRNASeq assumes that, if the data is strand specific, the sequencing was done using a protocol such as the Illumina TruSeq, where the reverse strand is quantified - i.e. the strandProtocol argument of the BamParam class defaults to 'reverse'.
> 
> # cleanup
> # removebfc(easyRNASeq:::.get_cache(),ask=FALSE)
> 
> proc.time()
   user  system elapsed 
 110.70    2.76  137.04 

Example timings

easyRNASeq.Rcheck/examples_i386/easyRNASeq-Ex.timings

nameusersystemelapsed
BiocFileCache-methods21.79 1.2337.83
DESeq-methods000
GenomicRanges-methods0.440.040.47
IRanges-methods000
Rsamtools-methods12.11 0.5114.75
ShortRead-methods000
easyRNASeq-AnnotParam-accessors0.760.050.90
easyRNASeq-AnnotParam-class000
easyRNASeq-AnnotParam0.800.010.91
easyRNASeq-BamFileList14.92 0.7153.44
easyRNASeq-BamParam-accessors000
easyRNASeq-BamParam-class000
easyRNASeq-BamParam0.020.000.01
easyRNASeq-RnaSeqParam-accessors000
easyRNASeq-RnaSeqParam-class000
easyRNASeq-RnaSeqParam0.010.000.02
easyRNASeq-accessors000
easyRNASeq-annotation-methods000
easyRNASeq-class000
easyRNASeq-correction-methods000
easyRNASeq-coverage-methods000
easyRNASeq-easyRNASeq000
easyRNASeq-island-methods000
easyRNASeq-package61.14 3.5668.45
easyRNASeq-simpleRNASeq123.66 0.84128.94
easyRNASeq-summarization-methods000
easyRNASeq-synthetic-transcripts43.75 0.0844.41
edgeR-methods000
genomeIntervals-methods1.580.172.14
parallel-methods000

easyRNASeq.Rcheck/examples_x64/easyRNASeq-Ex.timings

nameusersystemelapsed
BiocFileCache-methods 22.14 1.06117.42
DESeq-methods000
GenomicRanges-methods0.300.040.33
IRanges-methods000
Rsamtools-methods11.56 0.5113.89
ShortRead-methods000
easyRNASeq-AnnotParam-accessors0.800.061.00
easyRNASeq-AnnotParam-class000
easyRNASeq-AnnotParam0.780.040.94
easyRNASeq-BamFileList15.16 0.5390.11
easyRNASeq-BamParam-accessors000
easyRNASeq-BamParam-class000
easyRNASeq-BamParam0.010.000.01
easyRNASeq-RnaSeqParam-accessors000
easyRNASeq-RnaSeqParam-class000
easyRNASeq-RnaSeqParam0.020.000.02
easyRNASeq-accessors000
easyRNASeq-annotation-methods000
easyRNASeq-class000
easyRNASeq-correction-methods000
easyRNASeq-coverage-methods000
easyRNASeq-easyRNASeq000
easyRNASeq-island-methods000
easyRNASeq-package55.39 1.2159.93
easyRNASeq-simpleRNASeq108.18 0.90111.06
easyRNASeq-summarization-methods000
easyRNASeq-synthetic-transcripts37.88 0.0338.62
edgeR-methods000
genomeIntervals-methods2.090.212.63
parallel-methods000