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BUILD report for VariantAnnotation on malbec2

This page was generated on 2018-10-17 08:23:46 -0400 (Wed, 17 Oct 2018).

Package 1531/1561HostnameOS / ArchINSTALLBUILDCHECKBUILD BIN
VariantAnnotation 1.26.1
Valerie Obenchain
Snapshot Date: 2018-10-15 16:45:08 -0400 (Mon, 15 Oct 2018)
URL: https://git.bioconductor.org/packages/VariantAnnotation
Branch: RELEASE_3_7
Last Commit: 60ae675
Last Changed Date: 2018-07-04 14:09:06 -0400 (Wed, 04 Jul 2018)
malbec2 Linux (Ubuntu 16.04.1 LTS) / x86_64  OK [ ERROR ] skipped 
tokay2 Windows Server 2012 R2 Standard / x64  OK  OK  WARNINGS  OK UNNEEDED, same version exists in internal repository
merida2 OS X 10.11.6 El Capitan / x86_64  OK  OK  OK  OK UNNEEDED, same version exists in internal repository

Summary

Package: VariantAnnotation
Version: 1.26.1
Command: /home/biocbuild/bbs-3.7-bioc/R/bin/R CMD build --keep-empty-dirs --no-resave-data VariantAnnotation
StartedAt: 2018-10-15 19:19:27 -0400 (Mon, 15 Oct 2018)
EndedAt: 2018-10-15 19:21:24 -0400 (Mon, 15 Oct 2018)
EllapsedTime: 116.4 seconds
RetCode: 1
Status:  ERROR 
PackageFile: None
PackageFileSize: NA

Command output

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### Running command:
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###   /home/biocbuild/bbs-3.7-bioc/R/bin/R CMD build --keep-empty-dirs --no-resave-data VariantAnnotation
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* checking for file ‘VariantAnnotation/DESCRIPTION’ ... OK
* preparing ‘VariantAnnotation’:
* checking DESCRIPTION meta-information ... OK
* cleaning src
* installing the package to build vignettes
* creating vignettes ... ERROR
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, sd, var, xtabs

The following objects are masked from ‘package:base’:

    Filter, Find, Map, Position, Reduce, anyDuplicated, append,
    as.data.frame, basename, cbind, colMeans, colSums,
    colnames, dirname, 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, rowMeans, rowSums, rownames, sapply,
    setdiff, sort, table, tapply, union, unique, unsplit,
    which, which.max, which.min

Loading required package: GenomeInfoDb
Loading required package: S4Vectors
Loading required package: stats4

Attaching package: ‘S4Vectors’

The following object is masked from ‘package:base’:

    expand.grid

Loading required package: IRanges
Loading required package: GenomicRanges
Loading required package: SummarizedExperiment
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")'.

Loading required package: DelayedArray
Loading required package: matrixStats

Attaching package: ‘matrixStats’

The following objects are masked from ‘package:Biobase’:

    anyMissing, rowMedians

Loading required package: BiocParallel

Attaching package: ‘DelayedArray’

The following objects are masked from ‘package:matrixStats’:

    colMaxs, colMins, colRanges, rowMaxs, rowMins, rowRanges

The following objects are masked from ‘package:base’:

    aperm, apply

Loading required package: Rsamtools
Loading required package: Biostrings
Loading required package: XVector

Attaching package: ‘Biostrings’

The following object is masked from ‘package:DelayedArray’:

    type

The following object is masked from ‘package:base’:

    strsplit


Attaching package: ‘VariantAnnotation’

The following object is masked from ‘package:base’:

    tabulate

  Please note that the SNPlocs.Hsapiens.dbSNP.20101109 package
  contains outdated dbSNP data and will be deprecated in the near
  future. We highly recommend that you use a SNPlocs package
  based on a more recent dbSNP build for your analyses instead.
  See available.SNPs() for the list of SNPlocs packages currently
  available and make sure to pick up the most recent one.
Loading required package: GenomicFeatures
Loading required package: AnnotationDbi
Warning in valid.GenomicRanges.seqinfo(x, suggest.trim = TRUE) :
  GRanges object contains 2405 out-of-bound ranges located on
  sequences 75253, 74357, 74359, 74360, 74361, 74362, 74363,
  74358, 74364, 74365, 75254, 75259, 74368, 74369, 74366, 74367,
  74370, 74372, 74373, 74374, 74375, 74378, 74377, 74380, 74381,
  75262, 75263, 75265, 75266, 75268, 75269, 75271, 75273, 75276,
  75281, 75282, 75283, 74389, 74383, 74384, 74385, 74386, 74387,
  75287, 75288, 75286, 75289, 74390, 74391, 74392, 74393, 74394,
  75291, 74395, 74396, 74397, 74398, 75302, 75304, 75305, and
  75306. Note that ranges located on a sequence whose length is
  unknown (NA) or on a circular sequence are not considered
  out-of-bound (use seqlengths() and isCircular() to get the
  lengths and circularity flags of the underlying sequences). You
  can use trim() to trim these ranges. See
  ?`trim,GenomicRanges-method` for more information.
'select()' returned many:1 mapping between keys and columns
Loading required package: BSgenome
Loading required package: rtracklayer
Warning in valid.GenomicRanges.seqinfo(x, suggest.trim = TRUE) :
  GRanges object contains 2405 out-of-bound ranges located on
  sequences 75253, 74357, 74359, 74360, 74361, 74362, 74363,
  74358, 74364, 74365, 75254, 75259, 74368, 74369, 74366, 74367,
  74370, 74372, 74373, 74374, 74375, 74378, 74377, 74380, 74381,
  75262, 75263, 75265, 75266, 75268, 75269, 75271, 75273, 75276,
  75281, 75282, 75283, 74389, 74383, 74384, 74385, 74386, 74387,
  75287, 75288, 75286, 75289, 74390, 74391, 74392, 74393, 74394,
  75291, 74395, 74396, 74397, 74398, 75302, 75304, 75305, and
  75306. Note that ranges located on a sequence whose length is
  unknown (NA) or on a circular sequence are not considered
  out-of-bound (use seqlengths() and isCircular() to get the
  lengths and circularity flags of the underlying sequences). You
  can use trim() to trim these ranges. See
  ?`trim,GenomicRanges-method` for more information.
Loading required package: RSQLite
Warning: 228 keys not found in PolyPhen database: rs114264124 rs149209714 ... rs146628983 rs138319189

Attaching package: ‘Matrix’

The following object is masked from ‘package:VariantAnnotation’:

    expand

The following object is masked from ‘package:S4Vectors’:

    expand

non-single nucleotide variations are set to NA
non-single nucleotide variations are set to NA
non-single nucleotide variations are set to NA
starting prefilter
prefiltering 3791 records
prefiltered to /tmp/RtmpotHKZZ/file720a423540a8
prefilter compressing and indexing ‘/tmp/RtmpotHKZZ/file720a423540a8’
starting filter
filtering 48 records
completed filtering

Attaching package: ‘AnnotationHub’

The following object is masked from ‘package:Biobase’:

    cache


Error: processing vignette 'filterVcf.Rnw' failed with diagnostics:
 chunk 6 (label = mcf7regulatoryRegions) 
Error in value[[3L]](cond) : failed to connect
  reason: Timeout was reached: Resolving timed out after 10000 milliseconds
  Consider rerunning with 'localHub=TRUE'
Execution halted