Mercurial > repos > iuc > rgrnastar

comparison test-data/rnastar_test_mapped_reads.vcf @ 28:3e94726bfa9d draft

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planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/rgrnastar commit 452556bcdcc3fe4e9ace07201be2365cd6f99e2f
author iuc
date Sun, 11 Feb 2024 00:01:54 +0000
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27:79de45b5069b 28:3e94726bfa9d
1 ##fileformat=VCFv4.2
2 ##FILTER=<ID=PASS,Description="All filters passed">
3 ##bcftoolsVersion=1.13+htslib-1.13+ds
4 ##bcftoolsCommand=mpileup -Ob -o rnastar_test_mapped_reads.bcf -f tophat_test.fa rnastar_test_mapped_reads.bam
5 ##reference=file://tophat_test.fa
6 ##contig=<ID=test_chromosome,length=650>
7 ##ALT=<ID=*,Description="Represents allele(s) other than observed.">
8 ##INFO=<ID=INDEL,Number=0,Type=Flag,Description="Indicates that the variant is an INDEL.">
9 ##INFO=<ID=IDV,Number=1,Type=Integer,Description="Maximum number of raw reads supporting an indel">
10 ##INFO=<ID=IMF,Number=1,Type=Float,Description="Maximum fraction of raw reads supporting an indel">
11 ##INFO=<ID=DP,Number=1,Type=Integer,Description="Raw read depth">
12 ##INFO=<ID=VDB,Number=1,Type=Float,Description="Variant Distance Bias for filtering splice-site artefacts in RNA-seq data (bigger is better)",Version="3">
13 ##INFO=<ID=RPBZ,Number=1,Type=Float,Description="Mann-Whitney U-z test of Read Position Bias (closer to 0 is better)">
14 ##INFO=<ID=MQBZ,Number=1,Type=Float,Description="Mann-Whitney U-z test of Mapping Quality Bias (closer to 0 is better)">
15 ##INFO=<ID=BQBZ,Number=1,Type=Float,Description="Mann-Whitney U-z test of Base Quality Bias (closer to 0 is better)">
16 ##INFO=<ID=MQSBZ,Number=1,Type=Float,Description="Mann-Whitney U-z test of Mapping Quality vs Strand Bias (closer to 0 is better)">
17 ##INFO=<ID=SCBZ,Number=1,Type=Float,Description="Mann-Whitney U-z test of Soft-Clip Length Bias (closer to 0 is better)">
18 ##INFO=<ID=FS,Number=1,Type=Float,Description="Phred-scaled p-value using Fisher's exact test to detect strand bias">
19 ##INFO=<ID=SGB,Number=1,Type=Float,Description="Segregation based metric.">
20 ##INFO=<ID=MQ0F,Number=1,Type=Float,Description="Fraction of MQ0 reads (smaller is better)">
21 ##FORMAT=<ID=PL,Number=G,Type=Integer,Description="List of Phred-scaled genotype likelihoods">
22 ##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
23 ##INFO=<ID=AC,Number=A,Type=Integer,Description="Allele count in genotypes for each ALT allele, in the same order as listed">
24 ##INFO=<ID=AN,Number=1,Type=Integer,Description="Total number of alleles in called genotypes">
25 ##INFO=<ID=DP4,Number=4,Type=Integer,Description="Number of high-quality ref-forward , ref-reverse, alt-forward and alt-reverse bases">
26 ##INFO=<ID=MQ,Number=1,Type=Integer,Description="Average mapping quality">
27 ##bcftools_callVersion=1.13+htslib-1.13+ds
28 ##bcftools_callCommand=call -vmO z -o rnastar_test_mapped_reads.vcf.gz rnastar_test_mapped_reads.bcf; Date=Tue Jan 2 11:53:57 2024
29 #CHROM POS ID REF ALT QUAL FILTER INFO FORMAT rnastar_test_mapped_reads.bam
30 test_chromosome 219 . G C 170.416 . DP=27;VDB=0.505999;SGB=-0.693021;FS=0;MQ0F=0;AC=2;AN=2;DP4=0,0,7,20;MQ=20 GT:PL 1/1:200,81,0