|
2
|
1 ##fileformat=VCFv4.1
|
|
|
2 ##INFO=<ID=DP,Number=1,Type=Integer,Description="Raw read depth">
|
|
|
3 ##INFO=<ID=DP4,Number=4,Type=Integer,Description="# high-quality ref-forward bases, ref-reverse, alt-forward and alt-reverse bases">
|
|
|
4 ##INFO=<ID=MQ,Number=1,Type=Integer,Description="Root-mean-square mapping quality of covering reads">
|
|
|
5 ##INFO=<ID=FQ,Number=1,Type=Float,Description="Phred probability of all samples being the same">
|
|
|
6 ##INFO=<ID=AF1,Number=1,Type=Float,Description="Max-likelihood estimate of the first ALT allele frequency (assuming HWE)">
|
|
|
7 ##INFO=<ID=AC1,Number=1,Type=Float,Description="Max-likelihood estimate of the first ALT allele count (no HWE assumption)">
|
|
|
8 ##INFO=<ID=AN,Number=1,Type=Integer,Description="Total number of alleles in called genotypes">
|
|
|
9 ##INFO=<ID=IS,Number=2,Type=Float,Description="Maximum number of reads supporting an indel and fraction of indel reads">
|
|
|
10 ##INFO=<ID=AC,Number=A,Type=Integer,Description="Allele count in genotypes for each ALT allele, in the same order as listed">
|
|
|
11 ##INFO=<ID=G3,Number=3,Type=Float,Description="ML estimate of genotype frequencies">
|
|
|
12 ##INFO=<ID=HWE,Number=1,Type=Float,Description="Chi^2 based HWE test P-value based on G3">
|
|
|
13 ##INFO=<ID=CLR,Number=1,Type=Integer,Description="Log ratio of genotype likelihoods with and without the constraint">
|
|
|
14 ##INFO=<ID=UGT,Number=1,Type=String,Description="The most probable unconstrained genotype configuration in the trio">
|
|
|
15 ##INFO=<ID=CGT,Number=1,Type=String,Description="The most probable constrained genotype configuration in the trio">
|
|
|
16 ##INFO=<ID=PV4,Number=4,Type=Float,Description="P-values for strand bias, baseQ bias, mapQ bias and tail distance bias">
|
|
|
17 ##INFO=<ID=INDEL,Number=0,Type=Flag,Description="Indicates that the variant is an INDEL.">
|
|
|
18 ##INFO=<ID=PC2,Number=2,Type=Integer,Description="Phred probability of the nonRef allele frequency in group1 samples being larger (,smaller) than in group2.">
|
|
|
19 ##INFO=<ID=PCHI2,Number=1,Type=Float,Description="Posterior weighted chi^2 P-value for testing the association between group1 and group2 samples.">
|
|
|
20 ##INFO=<ID=QCHI2,Number=1,Type=Integer,Description="Phred scaled PCHI2.">
|
|
|
21 ##INFO=<ID=PR,Number=1,Type=Integer,Description="# permutations yielding a smaller PCHI2.">
|
|
|
22 ##INFO=<ID=QBD,Number=1,Type=Float,Description="Quality by Depth: QUAL/#reads">
|
|
|
23 ##INFO=<ID=RPB,Number=1,Type=Float,Description="Read Position Bias">
|
|
|
24 ##INFO=<ID=MDV,Number=1,Type=Integer,Description="Maximum number of high-quality nonRef reads in samples">
|
|
|
25 ##INFO=<ID=VDB,Number=1,Type=Float,Description="Variant Distance Bias (v2) for filtering splice-site artefacts in RNA-seq data. Note: this version may be broken.">
|
|
|
26 ##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
|
|
|
27 ##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
|
|
|
28 ##FORMAT=<ID=GL,Number=3,Type=Float,Description="Likelihoods for RR,RA,AA genotypes (R=ref,A=alt)">
|
|
|
29 ##FORMAT=<ID=DP,Number=1,Type=Integer,Description="# high-quality bases">
|
|
|
30 ##FORMAT=<ID=DV,Number=1,Type=Integer,Description="# high-quality non-reference bases">
|
|
|
31 ##FORMAT=<ID=SP,Number=1,Type=Integer,Description="Phred-scaled strand bias P-value">
|
|
|
32 ##FORMAT=<ID=PL,Number=G,Type=Integer,Description="List of Phred-scaled genotype likelihoods">
|
|
|
33 #CHROM POS ID REF ALT QUAL FILTER INFO FORMAT
|
