'\" t .TH vcf 5 "August 2013" "htslib" "Bioinformatics formats" .SH NAME vcf \- Variant Call Format .\" .\" Copyright (C) 2011 Broad Institute. .\" Copyright (C) 2013-2014 Genome Research Ltd. .\" .\" Author: Heng Li .\" .\" Permission is hereby granted, free of charge, to any person obtaining a .\" copy of this software and associated documentation files (the "Software"), .\" to deal in the Software without restriction, including without limitation .\" the rights to use, copy, modify, merge, publish, distribute, sublicense, .\" and/or sell copies of the Software, and to permit persons to whom the .\" Software is furnished to do so, subject to the following conditions: .\" .\" The above copyright notice and this permission notice shall be included in .\" all copies or substantial portions of the Software. .\" .\" THE SOFTWARE IS PROVIDED "AS IS", WITHOUT WARRANTY OF ANY KIND, EXPRESS OR .\" IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY, .\" FITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT. IN NO EVENT SHALL .\" THE AUTHORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY CLAIM, DAMAGES OR OTHER .\" LIABILITY, WHETHER IN AN ACTION OF CONTRACT, TORT OR OTHERWISE, ARISING .\" FROM, OUT OF OR IN CONNECTION WITH THE SOFTWARE OR THE USE OR OTHER .\" DEALINGS IN THE SOFTWARE. .\" .SH DESCRIPTION The Variant Call Format (VCF) is a TAB-delimited format with each data line consisting of the following fields: .TS nlbl. 1 CHROM CHROMosome name 2 POS the left-most POSition of the variant 3 ID unique variant IDentifier 4 REF the REFerence allele 5 ALT the ALTernate allele(s) (comma-separated) 6 QUAL variant/reference QUALity 7 FILTER FILTERs applied 8 INFO INFOrmation related to the variant (semicolon-separated) 9 FORMAT FORMAT of the genotype fields (optional; colon-separated) 10+ SAMPLE SAMPLE genotypes and per-sample information (optional) .TE .P The following table gives the \fBINFO\fP tags used by samtools and bcftools. .TP .B AF1 Max-likelihood estimate of the site allele frequency (AF) of the first ALT allele (double) .TP .B DP Raw read depth (without quality filtering) (int) .TP .B DP4 # high-quality reference forward bases, ref reverse, alternate for and alt rev bases (int[4]) .TP .B FQ Consensus quality. Positive: sample genotypes different; negative: otherwise (int) .TP .B MQ Root-Mean-Square mapping quality of covering reads (int) .TP .B PC2 Phred probability of AF in group1 samples being larger (,smaller) than in group2 (int[2]) .TP .B PCHI2 Posterior weighted chi^2 P-value between group1 and group2 samples (double) .TP .B PV4 P-value for strand bias, baseQ bias, mapQ bias and tail distance bias (double[4]) .TP .B QCHI2 Phred-scaled PCHI2 (int) .TP .B RP # permutations yielding a smaller PCHI2 (int) .TP .B CLR Phred log ratio of genotype likelihoods with and without the trio/pair constraint (int) .TP .B UGT Most probable genotype configuration without the trio constraint (string) .TP .B CGT Most probable configuration with the trio constraint (string) .TP .B VDB Tests variant positions within reads. Intended for filtering RNA-seq artifacts around splice sites (float) .TP .B RPB Mann-Whitney rank-sum test for tail distance bias (float) .TP .B HWE Hardy-Weinberg equilibrium test (Wigginton et al) (float) .P .SH SEE ALSO .TP https://github.com/samtools/hts-specs The full VCF/BCF file format specification .TP .I A note on exact tests of Hardy-Weinberg equilibrium Wigginton JE et al PMID:15789306 .\" (http://www.ncbi.nlm.nih.gov/pubmed/15789306)