File: vcfflatten.1

package info (click to toggle)
libvcflib 1.0.2%2Bdfsg-2
  • links: PTS, VCS
  • area: main
  • in suites: bullseye
  • size: 49,732 kB
  • sloc: cpp: 39,194; perl: 474; python: 321; ruby: 285; sh: 247; ansic: 198; makefile: 125; javascript: 94; lisp: 55
file content (42 lines) | stat: -rw-r--r-- 824 bytes parent folder | download
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
.\" Automatically generated by Pandoc 2.7.3
.\"
.TH "VCFFLATTEN" "1" "" "vcfflatten (vcflib)" "vcfflatten (VCF transformation)"
.hy
.SH NAME
.PP
\f[B]vcfflatten\f[R]
.SH SYNOPSIS
.PP
\f[B]vcfflatten\f[R] [file]
.SH DESCRIPTION
.PP
Removes multi-allelic sites by picking the most common alternate.
Requires allele frequency specification `AF' and use of `G' and `A' to
specify the fields which vary according to the Allele or Genotype.
VCF file may be specified on the command line or piped as stdin.
.SH OPTIONS
.IP
.nf
\f[C]


Type: transformation
\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.