Entering edit mode
Hi all,
I am interested in reading in only a subset of the subjects contained
in a large multi-sample vcf file. As far as I can see, there is a lot
of great functionality in VariantAnnotation for subsetting vcfs based
on genomic coordinates, annotation, etc. but I can't see anything for
subsetting samples, either in the current release or the devel
version. Any help would be greatly appreciated!
Cheers,
Margaret
Margaret Taub, PhD
Assistant Scientist
Department of Biostatistics
Johns Hopkins University
Bloomberg School of Public Health, E3546
410-614-9408
mtaub@jhsph.edu<mailto:mtaub@jhsph.edu>
> sessionInfo()
R version 2.15.2 Patched (2013-02-08 r61876)
Platform: x86_64-unknown-linux-gnu (64-bit)
locale:
[1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
[3] LC_TIME=en_US.utf-8 LC_COLLATE=en_US.utf-8
[5] LC_MONETARY=en_US.utf-8 LC_MESSAGES=en_US.utf-8
[7] LC_PAPER=C LC_NAME=C
[9] LC_ADDRESS=C LC_TELEPHONE=C
[11] LC_MEASUREMENT=en_US.iso885915 LC_IDENTIFICATION=C
attached base packages:
[1] stats graphics grDevices datasets utils methods base
other attached packages:
[1] VariantAnnotation_1.4.12 Rsamtools_1.10.2
Biostrings_2.26.3
[4] GenomicRanges_1.10.6 IRanges_1.16.4
BiocGenerics_0.4.0
[7] RColorBrewer_1.0-5
loaded via a namespace (and not attached):
[1] AnnotationDbi_1.20.3 Biobase_2.18.0 biomaRt_2.14.0
[4] bitops_1.0-5 BSgenome_1.26.1 DBI_0.2-5
[7] GenomicFeatures_1.10.1 parallel_2.15.2 RCurl_1.95-3
[10] RSQLite_0.11.2 rtracklayer_1.18.2 stats4_2.15.2
[13] tools_2.15.2 XML_3.95-0.1 zlibbioc_1.4.0
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