Variant Call Format
| Filename extension |
.vcf |
|---|---|
| Developed by | 1000 Genomes Project |
| Latest release | 4.5 June 28, 2024 |
| Type of format | Bioinformatics |
| Extended from | Tab-separated values |
| Extended to | gVCF |
| Open format? | Yes |
| Website | samtools |
The Variant Call Format or VCF is a standard text file format used in bioinformatics for storing gene sequence or DNA sequence variations. The format was developed in 2010 for the 1000 Genomes Project and has since been used by other large-scale genotyping and DNA sequencing projects.[1][2] VCF is a common output format for variant calling programs due to its relative simplicity and scalability.[3][4] Many tools have been developed for editing and manipulating VCF files, including VCFtools, which was released in conjunction with the VCF format in 2011, and BCFtools, which was included as part of SAMtools until being split into an independent package in 2014.[1][5]
The standard is currently in version 4.5,[6][7] although the 1000 Genomes Project has developed its own specification for structural variations such as duplications, which are not easily accommodated into the existing schema.[8]
Additional file formats have been developed based on VCF, including genomic VCF (gVCF). gVCF is an extended format which includes additional information about "blocks" that match the reference and their qualities.[9][10]
Example
[edit]##fileformat=VCFv4.3 ##fileDate=20090805 ##source=myImputationProgramV3.1 ##reference=file:///seq/references/1000GenomesPilot-NCBI36.fasta ##contig=<ID=20,length=62435964,assembly=B36,md5=f126cdf8a6e0c7f379d618ff66beb2da,species="Homo sapiens",taxonomy=x> ##phasing=partial ##INFO=<ID=NS,Number=1,Type=Integer,Description="Number of Samples With Data"> ##INFO=<ID=DP,Number=1,Type=Integer,Description="Total Depth"> ##INFO=<ID=AF,Number=A,Type=Float,Description="Allele Frequency"> ##INFO=<ID=AA,Number=1,Type=String,Description="Ancestral Allele"> ##INFO=<ID=DB,Number=0,Type=Flag,Description="dbSNP membership, build 129"> ##INFO=<ID=H2,Number=0,Type=Flag,Description="HapMap2 membership"> ##FILTER=<ID=q10,Description="Quality below 10"> ##FILTER=<ID=s50,Description="Less than 50% of samples have data"> ##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype"> ##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality"> ##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read Depth"> ##FORMAT=<ID=HQ,Number=2,Type=Integer,Description="Haplotype Quality"> #CHROM POS ID REF ALT QUAL FILTER INFO FORMAT NA00001 NA00002 NA00003 20 14370 rs6054257 G A 29 PASS NS=3;DP=14;AF=0.5;DB;H2 GT:GQ:DP:HQ 0|0:48:1:51,51 1|0:48:8:51,51 1/1:43:5:.,. 20 17330 . T A 3 q10 NS=3;DP=11;AF=0.017 GT:GQ:DP:HQ 0|0:49:3:58,50 0|1:3:5:65,3 0/0:41:3 20 1110696 rs6040355 A G,T 67 PASS NS=2;DP=10;AF=0.333,0.667;AA=T;DB GT:GQ:DP:HQ 1|2:21:6:23,27 2|1:2:0:18,2 2/2:35:4 20 1230237 . T . 47 PASS NS=3;DP=13;AA=T GT:GQ:DP:HQ 0|0:54:7:56,60 0|0:48:4:51,51 0/0:61:2 20 1234567 microsat1 GTC G,GTCT 50 PASS NS=3;DP=9;AA=G GT:GQ:DP 0/1:35:4 0/2:17:2 1/1:40:3
The VCF header
[edit]The header begins the file and provides metadata describing the body of the file. Header lines are denoted as starting with #. Special keywords in the header are denoted with ##. Recommended keywords include fileformat, fileDate and reference.
The header contains keywords that optionally semantically and syntactically describe the fields used in the body of the file, notably INFO, FILTER, and FORMAT (see below).
The columns of a VCF
[edit]The body of VCF follows the header, and is tab separated into 8 mandatory columns and an unlimited number of optional columns that may be used to record other information about the sample(s). When additional columns are used, the first optional column is used to describe the format of the data in the columns that follow.
| Name | Brief description (see the specification for details). | |
|---|---|---|
| 1 | CHROM | The name of the sequence (typically a chromosome) on which the variation is being called. This sequence is usually known as 'the reference sequence', i.e. the sequence against which the given sample varies. |
| 2 | POS | The 1-based position of the variation on the given sequence. |
| 3 | ID | The identifier of the variation, e.g. a dbSNP rs identifier, or if unknown a ".". Multiple identifiers should be separated by semi-colons without white-space. |
| 4 | REF | The reference base (or bases in the case of an indel) at the given position on the given reference sequence. |
| 5 | ALT | The list of alternative alleles at this position. |
| 6 | QUAL | A quality score associated with the inference of the given alleles. |
| 7 | FILTER | A flag indicating which of a given set of filters the variation has failed or PASS if all the filters were passed successfully. |
| 8 | INFO | An extensible list of key-value pairs (fields) describing the variation. See below for some common fields. Multiple fields are separated by semicolons with optional values in the format: <key>=<data>[,data].
|
| 9 | FORMAT | An (optional) extensible list of fields for describing the samples. See below for some common fields. |
| + | SAMPLEs | For each (optional) sample described in the file, values are given for the fields listed in FORMAT |
Common INFO fields
[edit]Arbitrary keys are permitted, although the following sub-fields are reserved (albeit optional):[6]
| Name | Brief description |
|---|---|
| AA | ancestral allele |
| AC | allele count in genotypes, for each ALT allele, in the same order as listed |
| AF | allele frequency for each ALT allele in the same order as listed (use this when estimated from primary data, not called genotypes) |
| AN | total number of alleles in called genotypes |
| BQ | RMS base quality at this position |
| CIGAR | cigar string describing how to align an alternate allele to the reference allele |
| DB | dbSNP membership |
| DP | combined depth across samples, e.g. DP=154 |
| END | end position of the variant described in this record (for use with symbolic alleles) |
| H2 | membership in hapmap2 |
| H3 | membership in hapmap3 |
| MQ | RMS mapping quality, e.g. MQ=52 |
| MQ0 | Number of MAPQ == 0 reads covering this record |
| NS | Number of samples with data |
| SB | strand bias at this position |
| SOMATIC | indicates that the record is a somatic mutation, for cancer genomics |
| VALIDATED | validated by follow-up experiment |
| 1000G | membership in 1000 Genomes |
Any other info fields are defined in the .vcf header.
Common FORMAT fields
[edit]| Name | Brief description |
|---|---|
| AD | Read depth for each allele |
| ADF | Read depth for each allele on the forward strand |
| ADR | Read depth for each allele on the reverse strand |
| DP | Read depth |
| EC | Expected alternate allele counts |
| FT | Filter indicating if this genotype was “called” |
| GL | Genotype likelihoods |
| GP | Genotype posterior probabilities |
| GQ | Conditional genotype quality |
| GT | Genotype |
| HQ | Haplotype quality |
| MQ | RMS mapping quality |
| PL | Phred-scaled genotype likelihoods rounded to the closest integer |
| PQ | Phasing quality |
| PS | Phase set |
Any other format fields are defined in the .vcf header.
See also
[edit]- The FASTA format, used to represent genome sequences.
- The FASTQ format, used to represent DNA sequencer reads along with quality scores.
- The SAM format, used to represent genome sequencer reads that have been aligned to genome sequences.
- The GVF format (Genome Variation Format), an extension based on the GFF3 format.
- Global Alliance for Genomics and Health (GA4GH), the group leading the management and expansion of the VCF format.[11] The VCF specification is no longer maintained by the 1000 Genomes Project.[12]
References
[edit]- ^ a b Danecek, Petr; Auton, Adam; Abecasis, Goncalo; Albers, Cornelis A.; Banks, Eric; DePristo, Mark A.; Handsaker, Robert E.; Lunter, Gerton; Marth, Gabor T.; Sherry, Stephen T.; McVean, Gilean; Durbin, Richard (2011-08-01). "The variant call format and VCFtools". Bioinformatics. 27 (15): 2156–2158. doi:10.1093/bioinformatics/btr330. ISSN 1367-4803. PMC 3137218. PMID 21653522.
- ^ Ossola, Alexandra (20 March 2015). "The Race to Build a Search Engine for Your DNA". IEEE Spectrum. Retrieved 22 March 2015.
- ^ "Understanding VCF format | Human genetic variation". EMBL-EBI. Archived from the original on 2023-04-20. Retrieved 2023-11-10.
- ^ Garrison, Erik; Kronenberg, Zev N.; Dawson, Eric T.; Pedersen, Brent S.; Prins, Pjotr (2022-05-31). "A spectrum of free software tools for processing the VCF variant call format: vcflib, bio-vcf, cyvcf2, hts-nim and slivar". PLOS Computational Biology. 18 (5): e1009123. Bibcode:2022PLSCB..18E9123G. doi:10.1371/journal.pcbi.1009123. ISSN 1553-734X. PMC 9286226. PMID 35639788.
- ^ Danecek, Petr; Bonfield, James K; Liddle, Jennifer; Marshall, John; Ohan, Valeriu; Pollard, Martin O; Whitwham, Andrew; Keane, Thomas; McCarthy, Shane A; Davies, Robert M; Li, Heng (2021-01-29). "Twelve years of SAMtools and BCFtools". GigaScience. 10 (2). doi:10.1093/gigascience/giab008. ISSN 2047-217X. PMC 7931819. PMID 33590861.
- ^ a b "VCF Specification" (PDF). Retrieved 30 July 2024.
- ^ "Specifications of SAM/BAM and related high-throughput sequencing file formats". GitHub. Retrieved 24 June 2014.
- ^ "Encoding Structural Variants in VCF (Variant Call Format) version 4.0 | 1000 Genomes". Retrieved 20 October 2016.
- ^ "GVCF - Genomic Variant Call Format". GATK. Broad Institute.
- ^ "gVCF Files". Illumina, Inc. Retrieved 2023-11-10.
- ^ "HTS format specifications". samtools.github.io. Retrieved 2022-02-22.
- ^ "Bio-IT World". www.bio-itworld.com. Retrieved 2018-10-26.
