GSP
Quick Navigator

Search Site

Unix VPS
A - Starter
B - Basic
C - Preferred
D - Commercial
MPS - Dedicated
Previous VPSs
* Sign Up! *

Support
Contact Us
Online Help
Handbooks
Domain Status
Man Pages

FAQ
Virtual Servers
Pricing
Billing
Technical

Network
Facilities
Connectivity
Topology Map

Miscellaneous
Server Agreement
Year 2038
Credits
 

USA Flag

 

 

Man Pages
vcf(5) Bioinformatics formats vcf(5)

vcf - Variant Call Format

The Variant Call Format (VCF) is a TAB-delimited format with each data line consisting of the following fields:
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)
The following table gives the INFO tags used by samtools and bcftools.
AF1
Max-likelihood estimate of the site allele frequency (AF) of the first ALT allele (double)
DP
Raw read depth (without quality filtering) (int)
DP4
# high-quality reference forward bases, ref reverse, alternate for and alt rev bases (int[4])
FQ
Consensus quality. Positive: sample genotypes different; negative: otherwise (int)
MQ
Root-Mean-Square mapping quality of covering reads (int)
PC2
Phred probability of AF in group1 samples being larger (,smaller) than in group2 (int[2])
PCHI2
Posterior weighted chi^2 P-value between group1 and group2 samples (double)
PV4
P-value for strand bias, baseQ bias, mapQ bias and tail distance bias (double[4])
QCHI2
Phred-scaled PCHI2 (int)
RP
# permutations yielding a smaller PCHI2 (int)
CLR
Phred log ratio of genotype likelihoods with and without the trio/pair constraint (int)
UGT
Most probable genotype configuration without the trio constraint (string)
CGT
Most probable configuration with the trio constraint (string)
VDB
Tests variant positions within reads. Intended for filtering RNA-seq artifacts around splice sites (float)
RPB
Mann-Whitney rank-sum test for tail distance bias (float)
HWE
Hardy-Weinberg equilibrium test (Wigginton et al) (float)

https://github.com/samtools/hts-specs
The full VCF/BCF file format specification
A note on exact tests of Hardy-Weinberg equilibrium
Wigginton JE et al PMID:15789306
August 2013 htslib

Search for    or go to Top of page |  Section 5 |  Main Index

Powered by GSP Visit the GSP FreeBSD Man Page Interface.
Output converted with ManDoc.