Mercurial > repos > artbio > lumpy_smoove

comparison test-data/result-3.vcf @ 0:ee8fc44b1655 draft

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"planemo upload for repository https://github.com/ARTbio/tools-artbio/tree/master/tools/lumpy_smoove commit 515176ccca845de0b1a0c08417238bfa9ea45360"
author artbio
date Tue, 25 Aug 2020 11:35:02 -0400
parents
children 65b400409455
comparison
equal deleted inserted replaced
-1:000000000000 0:ee8fc44b1655
1 ##fileformat=VCFv4.2
2 ##contig=<ID=chrI,length=15072434>
3 ##smoove_version=0.2.5
4 ##reference=reference.fa
5 ##smoove_count_stats=tumor:2869,2691,202,330
6 ##smoove_count_stats=normal:2531,2421,156,296
7 ##source=LUMPY
8 ##INFO=<ID=SVTYPE,Number=1,Type=String,Description="Type of structural variant">
9 ##INFO=<ID=SVLEN,Number=.,Type=Integer,Description="Difference in length between REF and ALT alleles">
10 ##INFO=<ID=END,Number=1,Type=Integer,Description="End position of the variant described in this record">
11 ##INFO=<ID=STRANDS,Number=.,Type=String,Description="Strand orientation of the adjacency in BEDPE format (DEL:+-, DUP:-+, INV:++/--)">
12 ##INFO=<ID=IMPRECISE,Number=0,Type=Flag,Description="Imprecise structural variation">
13 ##INFO=<ID=CIPOS,Number=2,Type=Integer,Description="Confidence interval around POS for imprecise variants">
14 ##INFO=<ID=CIEND,Number=2,Type=Integer,Description="Confidence interval around END for imprecise variants">
15 ##INFO=<ID=CIPOS95,Number=2,Type=Integer,Description="Confidence interval (95%) around POS for imprecise variants">
16 ##INFO=<ID=CIEND95,Number=2,Type=Integer,Description="Confidence interval (95%) around END for imprecise variants">
17 ##INFO=<ID=MATEID,Number=.,Type=String,Description="ID of mate breakends">
18 ##INFO=<ID=EVENT,Number=1,Type=String,Description="ID of event associated to breakend">
19 ##INFO=<ID=SECONDARY,Number=0,Type=Flag,Description="Secondary breakend in a multi-line variants">
20 ##INFO=<ID=SU,Number=.,Type=Integer,Description="Number of pieces of evidence supporting the variant across all samples">
21 ##INFO=<ID=PE,Number=.,Type=Integer,Description="Number of paired-end reads supporting the variant across all samples">
22 ##INFO=<ID=SR,Number=.,Type=Integer,Description="Number of split reads supporting the variant across all samples">
23 ##INFO=<ID=BD,Number=.,Type=Integer,Description="Amount of BED evidence supporting the variant across all samples">
24 ##INFO=<ID=EV,Number=.,Type=String,Description="Type of LUMPY evidence contributing to the variant call">
25 ##INFO=<ID=PRPOS,Number=.,Type=String,Description="LUMPY probability curve of the POS breakend">
26 ##INFO=<ID=PREND,Number=.,Type=String,Description="LUMPY probability curve of the END breakend">
27 ##ALT=<ID=DEL,Description="Deletion">
28 ##ALT=<ID=DUP,Description="Duplication">
29 ##ALT=<ID=INV,Description="Inversion">
30 ##ALT=<ID=DUP:TANDEM,Description="Tandem duplication">
31 ##ALT=<ID=INS,Description="Insertion of novel sequence">
32 ##ALT=<ID=CNV,Description="Copy number variable region">
33 ##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
34 ##FORMAT=<ID=SU,Number=1,Type=Integer,Description="Number of pieces of evidence supporting the variant">
35 ##FORMAT=<ID=PE,Number=1,Type=Integer,Description="Number of paired-end reads supporting the variant">
36 ##FORMAT=<ID=SR,Number=1,Type=Integer,Description="Number of split reads supporting the variant">
37 ##FORMAT=<ID=BD,Number=1,Type=Integer,Description="Amount of BED evidence supporting the variant">
38 #CHROM POS ID REF ALT QUAL FILTER INFO FORMAT normal tumor
39 chrI 10416569 1 N <DUP> . . SVTYPE=DUP;STRANDS=-+:4;SVLEN=981;END=10417550;CIPOS=-769,29;CIEND=-30,636;CIPOS95=-165,8;CIEND95=-9,128;IMPRECISE;SU=4;PE=4;SR=0 GT:SU:PE:SR ./.:0:0:0 ./.:4:4:0