Mercurial > repos > devteam > vcftools_isec
comparison test-data/1.vcf @ 0:026d0f104183 draft
Uploaded
| author | devteam |
|---|---|
| date | Sun, 24 Nov 2013 14:03:51 -0500 |
| parents | |
| children |
comparison
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| -1:000000000000 | 0:026d0f104183 |
|---|---|
| 1 ##fileformat=VCFv4.1 | |
| 2 ##FILTER=<ID=indelError,Description="Likely artifact due to indel reads at this position"> | |
| 3 ##FILTER=<ID=str10,Description="Less than 10% or more than 90% of variant supporting reads on one strand"> | |
| 4 ##FORMAT=<ID=ABQ,Number=1,Type=Integer,Description="Average quality of variant-supporting bases (qual2)"> | |
| 5 ##FORMAT=<ID=AD,Number=1,Type=Integer,Description="Depth of variant-supporting bases (reads2)"> | |
| 6 ##FORMAT=<ID=ADF,Number=1,Type=Integer,Description="Depth of variant-supporting bases on forward strand (reads2plus)"> | |
| 7 ##FORMAT=<ID=ADR,Number=1,Type=Integer,Description="Depth of variant-supporting bases on reverse strand (reads2minus)"> | |
| 8 ##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Quality Read Depth of bases with Phred score >= 15"> | |
| 9 ##FORMAT=<ID=FREQ,Number=1,Type=String,Description="Variant allele frequency"> | |
| 10 ##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality"> | |
| 11 ##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype"> | |
| 12 ##FORMAT=<ID=PVAL,Number=1,Type=String,Description="P-value from Fisher's Exact Test"> | |
| 13 ##FORMAT=<ID=RBQ,Number=1,Type=Integer,Description="Average quality of reference-supporting bases (qual1)"> | |
| 14 ##FORMAT=<ID=RD,Number=1,Type=Integer,Description="Depth of reference-supporting bases (reads1)"> | |
| 15 ##FORMAT=<ID=RDF,Number=1,Type=Integer,Description="Depth of reference-supporting bases on forward strand (reads1plus)"> | |
| 16 ##FORMAT=<ID=RDR,Number=1,Type=Integer,Description="Depth of reference-supporting bases on reverse strand (reads1minus)"> | |
| 17 ##FORMAT=<ID=SDP,Number=1,Type=Integer,Description="Raw Read Depth as reported by SAMtools"> | |
| 18 ##INFO=<ID=ADP,Number=1,Type=Integer,Description="Average per-sample depth of bases with Phred score >= 15"> | |
| 19 ##INFO=<ID=HET,Number=1,Type=Integer,Description="Number of samples called heterozygous-variant"> | |
| 20 ##INFO=<ID=HOM,Number=1,Type=Integer,Description="Number of samples called homozygous-variant"> | |
| 21 ##INFO=<ID=NC,Number=1,Type=Integer,Description="Number of samples not called"> | |
| 22 ##INFO=<ID=WT,Number=1,Type=Integer,Description="Number of samples called reference (wild-type)"> | |
| 23 ##source=VarScan2 | |
| 24 #CHROM POS ID REF ALT QUAL FILTER INFO FORMAT Sample7 | |
| 25 chr1 14653 . C T . PASS ADP=30;HET=7;HOM=0;NC=0;WT=0 GT:GQ:SDP:DP:RD:AD:FREQ:PVAL:RBQ:ABQ:RDF:RDR:ADF:ADR 0/1:0:18:18:13:5:27.78%:9.8E-1:37:38:7:6:5:0 | |
| 26 chr1 14907 . A G . PASS ADP=18;HET=2;HOM=2;NC=1;WT=2 GT:GQ:SDP:DP:RD:AD:FREQ:PVAL:RBQ:ABQ:RDF:RDR:ADF:ADR 0/1:0:19:19:5:8:61.54%:9.8E-1:37:18:5:0:5:3 | |
| 27 chr1 14930 . A G . PASS ADP=19;HET=2;HOM=2;NC=1;WT=2 GT:GQ:SDP:DP:RD:AD:FREQ:PVAL:RBQ:ABQ:RDF:RDR:ADF:ADR 0/1:0:24:22:5:11:68.75%:9.8E-1:35:24:4:1:5:6 |