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.\" Automatically generated by Pandoc 2.7.3
.\"
.TH "VCFRANDOM" "1" "" "vcfrandom (vcflib)" "vcfrandom (VCF statistics)"
.hy
.SH NAME
.PP
\f[B]vcfrandom\f[R]
.SH SYNOPSIS
.PP
\f[B]vcfrandom\f[R]
.SH DESCRIPTION
.PP
Generate a random VCF file
.SH EXAMPLES
.IP
.nf
\f[C]
Example:
**vcfrandom**
##fileformat=VCFv4.0
##source=**vcfrandom**
##reference=/d2/data/references/build_37/human_reference_v37.fa
##phasing=none
##INFO=<ID=NS,Number=1,Type=Integer,Description=\[dq]Number of samples with data\[dq]>
##INFO=<ID=DP,Number=1,Type=Integer,Description=\[dq]Total read depth at the locus\[dq]>
##INFO=<ID=AC,Number=1,Type=Integer,Description=\[dq]Total number of alternate alleles in called genotypes\[dq]>
##INFO=<ID=AN,Number=1,Type=Integer,Description=\[dq]Total number of alleles in called genotypes\[dq]>
##INFO=<ID=AF,Number=1,Type=Float,Description=\[dq]Estimated allele frequency in the range (0,1]\[dq]>
##FORMAT=<ID=GT,Number=1,Type=String,Description=\[dq]Genotype\[dq]>
##FORMAT=<ID=GQ,Number=1,Type=Integer,Description=\[dq]Genotype Quality, the Phred-scaled marginal (or unconditional) probability of the called genotype\[dq]>
##FORMAT=<ID=DP,Number=1,Type=Integer,Description=\[dq]Read Depth\[dq]>
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT bill
one 1 . G G,A 100 . DP=83 GT:DP 0/1:1
one 2 . G G,A 100 . DP=3 GT:DP 0/1:49
one 3 . G C,T 100 . DP=5 GT:DP 0/1:12
one 4 . C G,T 100 . DP=51 GT:DP 0/1:60
one 5 . A T,A 100 . DP=31 GT:DP 0/1:89
one 6 . T T,A 100 . DP=56 GT:DP 0/1:60
one 7 . T A,C 100 . DP=78 GT:DP 0/1:75
one 8 . T G,A 100 . DP=73 GT:DP 0/1:78
one 9 . C C,G 100 . DP=42 GT:DP 0/1:67
Type: statistics
\f[R]
.fi
.SH EXIT VALUES
.TP
.B \f[B]0\f[R]
Success
.TP
.B \f[B]not 0\f[R]
Failure
.SH SEE ALSO
.PP
\f[B]vcflib\f[R](1)
.SH OTHER
.SH LICENSE
.PP
Copyright 2011-2020 (C) Erik Garrison and vcflib contributors.
MIT licensed.
.SH AUTHORS
Erik Garrison and vcflib contributors.
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