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62 changes: 62 additions & 0 deletions
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...er_worker__strucvars__ingest__header__test__build_output_header_37@sniffles2-min.vcf.snap
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--- | ||
source: src/strucvars/ingest/header.rs | ||
expression: "std::fs::read_to_string(out_path_str)?" | ||
--- | ||
##fileformat=VCFv4.4 | ||
##INFO=<ID=IMPRECISE,Number=0,Type=Flag,Description="Imprecise structural variation"> | ||
##INFO=<ID=END,Number=1,Type=Integer,Description="End position of the longest variant described in this record"> | ||
##INFO=<ID=SVTYPE,Number=1,Type=String,Description="Type of structural variant"> | ||
##INFO=<ID=SVLEN,Number=A,Type=Integer,Description="Length of structural variant"> | ||
##INFO=<ID=SVCLAIM,Number=A,Type=String,Description="Claim made by the structural variant call. Valid values are D, J, DJ for abundance, adjacency and both respectively"> | ||
##INFO=<ID=callers,Number=.,Type=String,Description="Callers that called the variant"> | ||
##INFO=<ID=chr2,Number=1,Type=String,Description="Second chromosome, if not equal to CHROM"> | ||
##INFO=<ID=annsv,Number=1,Type=String,Description="Effect annotations: 'Allele | Annotation | Gene_Name | Gene_ID'"> | ||
##FILTER=<ID=PASS,Description="All filters passed"> | ||
##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Conditional genotype quality"> | ||
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype"> | ||
##FORMAT=<ID=pec,Number=1,Type=Integer,Description="Total coverage with paired-end reads"> | ||
##FORMAT=<ID=pev,Number=1,Type=Integer,Description="Paired-end reads supporting the variant"> | ||
##FORMAT=<ID=src,Number=1,Type=Integer,Description="Total coverage with split reads"> | ||
##FORMAT=<ID=srv,Number=1,Type=Integer,Description="Split reads supporting the variant"> | ||
##FORMAT=<ID=amq,Number=1,Type=Float,Description="Average mapping quality over the variant"> | ||
##FORMAT=<ID=cn,Number=1,Type=Integer,Description="Copy number of the variant in the sample"> | ||
##FORMAT=<ID=anc,Number=1,Type=Float,Description="Average normalized coverage over the variant in the sample"> | ||
##FORMAT=<ID=pc,Number=1,Type=Integer,Description="Point count (windows/targets/probes)"> | ||
##ALT=<ID=DEL,Description="Deletion"> | ||
##ALT=<ID=DUP,Description="Duplication"> | ||
##ALT=<ID=INS,Description="Insertion"> | ||
##ALT=<ID=CNV,Description="Copy Number Variation"> | ||
##ALT=<ID=INV,Description="Inversion"> | ||
##contig=<ID=1,length=249250621,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=2,length=243199373,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=3,length=198022430,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=4,length=191154276,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=5,length=180915260,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=6,length=171115067,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=7,length=159138663,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=8,length=146364022,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=9,length=141213431,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=10,length=135534747,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=11,length=135006516,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=12,length=133851895,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=13,length=115169878,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=14,length=107349540,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=15,length=102531392,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=16,length=90354753,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=17,length=81195210,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=18,length=78077248,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=19,length=59128983,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=20,length=63025520,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=21,length=48129895,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=22,length=51304566,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=X,length=155270560,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=Y,length=59373566,assembly="GRCh37",species="Homo sapiens"> | ||
##contig=<ID=MT,length=16569,assembly="GRCh37",species="Homo sapiens"> | ||
##fileDate=20230421 | ||
##x-varfish-genome-build=GRCh37 | ||
##SAMPLE=<ID=SAMPLE,Sex="Male",Disease="Affected"> | ||
##PEDIGREE=<ID=SAMPLE> | ||
##x-varfish-case-uuid=d2bad2ec-a75d-44b9-bd0a-83a3f1331b7c | ||
##x-varfish-version=<ID=varfish-server-worker,Version="x.y.z"> | ||
##x-varfish-version=<ID=Sniffles2,Name="Sniffles2",Version="2.2"> | ||
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT SAMPLE |
62 changes: 62 additions & 0 deletions
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...er_worker__strucvars__ingest__header__test__build_output_header_38@sniffles2-min.vcf.snap
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--- | ||
source: src/strucvars/ingest/header.rs | ||
expression: "std::fs::read_to_string(out_path_str)?" | ||
--- | ||
##fileformat=VCFv4.4 | ||
##INFO=<ID=IMPRECISE,Number=0,Type=Flag,Description="Imprecise structural variation"> | ||
##INFO=<ID=END,Number=1,Type=Integer,Description="End position of the longest variant described in this record"> | ||
##INFO=<ID=SVTYPE,Number=1,Type=String,Description="Type of structural variant"> | ||
##INFO=<ID=SVLEN,Number=A,Type=Integer,Description="Length of structural variant"> | ||
##INFO=<ID=SVCLAIM,Number=A,Type=String,Description="Claim made by the structural variant call. Valid values are D, J, DJ for abundance, adjacency and both respectively"> | ||
##INFO=<ID=callers,Number=.,Type=String,Description="Callers that called the variant"> | ||
##INFO=<ID=chr2,Number=1,Type=String,Description="Second chromosome, if not equal to CHROM"> | ||
##INFO=<ID=annsv,Number=1,Type=String,Description="Effect annotations: 'Allele | Annotation | Gene_Name | Gene_ID'"> | ||
##FILTER=<ID=PASS,Description="All filters passed"> | ||
##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Conditional genotype quality"> | ||
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype"> | ||
##FORMAT=<ID=pec,Number=1,Type=Integer,Description="Total coverage with paired-end reads"> | ||
##FORMAT=<ID=pev,Number=1,Type=Integer,Description="Paired-end reads supporting the variant"> | ||
##FORMAT=<ID=src,Number=1,Type=Integer,Description="Total coverage with split reads"> | ||
##FORMAT=<ID=srv,Number=1,Type=Integer,Description="Split reads supporting the variant"> | ||
##FORMAT=<ID=amq,Number=1,Type=Float,Description="Average mapping quality over the variant"> | ||
##FORMAT=<ID=cn,Number=1,Type=Integer,Description="Copy number of the variant in the sample"> | ||
##FORMAT=<ID=anc,Number=1,Type=Float,Description="Average normalized coverage over the variant in the sample"> | ||
##FORMAT=<ID=pc,Number=1,Type=Integer,Description="Point count (windows/targets/probes)"> | ||
##ALT=<ID=DEL,Description="Deletion"> | ||
##ALT=<ID=DUP,Description="Duplication"> | ||
##ALT=<ID=INS,Description="Insertion"> | ||
##ALT=<ID=CNV,Description="Copy Number Variation"> | ||
##ALT=<ID=INV,Description="Inversion"> | ||
##contig=<ID=chr1,length=248956422,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr2,length=242193529,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr3,length=198295559,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr4,length=190214555,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr5,length=181538259,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr6,length=170805979,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr7,length=159345973,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr8,length=145138636,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr9,length=138394717,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr10,length=133797422,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr11,length=135086622,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr12,length=133275309,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr13,length=114364328,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr14,length=107043718,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr15,length=101991189,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr16,length=90338345,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr17,length=83257441,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr18,length=80373285,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr19,length=58617616,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr20,length=64444167,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr21,length=46709983,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chr22,length=50818468,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chrX,length=156040895,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chrY,length=57227415,assembly="GRCh38",species="Homo sapiens"> | ||
##contig=<ID=chrM,length=16569,assembly="GRCh38",species="Homo sapiens"> | ||
##fileDate=20230421 | ||
##x-varfish-genome-build=GRCh38 | ||
##SAMPLE=<ID=SAMPLE,Sex="Male",Disease="Affected"> | ||
##PEDIGREE=<ID=SAMPLE> | ||
##x-varfish-case-uuid=d2bad2ec-a75d-44b9-bd0a-83a3f1331b7c | ||
##x-varfish-version=<ID=varfish-server-worker,Version="x.y.z"> | ||
##x-varfish-version=<ID=Sniffles2,Name="Sniffles2",Version="2.2"> | ||
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT SAMPLE |
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FAM SAMPLE 0 0 1 2 |
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##fileformat=VCFv4.2 | ||
##source=Sniffles2_2.2 | ||
##command="sniffles --input out/SAMPLE.hac.sniffles.snf --vcf SAMPLE.multi.vcf" | ||
##fileDate="2024/02/09 14:19:35" | ||
##contig=<ID=1,length=249250621> | ||
##contig=<ID=2,length=243199373> | ||
##contig=<ID=3,length=198022430> | ||
##contig=<ID=4,length=191154276> | ||
##contig=<ID=5,length=180915260> | ||
##contig=<ID=6,length=171115067> | ||
##contig=<ID=7,length=159138663> | ||
##contig=<ID=8,length=146364022> | ||
##contig=<ID=9,length=141213431> | ||
##contig=<ID=10,length=135534747> | ||
##contig=<ID=11,length=135006516> | ||
##contig=<ID=12,length=133851895> | ||
##contig=<ID=13,length=115169878> | ||
##contig=<ID=14,length=107349540> | ||
##contig=<ID=15,length=102531392> | ||
##contig=<ID=16,length=90354753> | ||
##contig=<ID=17,length=81195210> | ||
##contig=<ID=18,length=78077248> | ||
##contig=<ID=19,length=59128983> | ||
##contig=<ID=20,length=63025520> | ||
##contig=<ID=21,length=48129895> | ||
##contig=<ID=22,length=51304566> | ||
##contig=<ID=X,length=155270560> | ||
##contig=<ID=Y,length=59373566> | ||
##contig=<ID=MT,length=16569> | ||
##ALT=<ID=INS,Description="Insertion"> | ||
##ALT=<ID=DEL,Description="Deletion"> | ||
##ALT=<ID=DUP,Description="Duplication"> | ||
##ALT=<ID=INV,Description="Inversion"> | ||
##ALT=<ID=BND,Description="Breakend; Translocation"> | ||
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype"> | ||
##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype quality"> | ||
##FORMAT=<ID=DR,Number=1,Type=Integer,Description="Number of reference reads"> | ||
##FORMAT=<ID=DV,Number=1,Type=Integer,Description="Number of variant reads"> | ||
##FORMAT=<ID=ID,Number=1,Type=String,Description="Individual sample SV ID for multi-sample output"> | ||
##FILTER=<ID=PASS,Description="All filters passed"> | ||
##FILTER=<ID=GT,Description="Genotype filter"> | ||
##FILTER=<ID=SUPPORT_MIN,Description="Minimum read support filter"> | ||
##FILTER=<ID=STDEV_POS,Description="SV Breakpoint standard deviation filter"> | ||
##FILTER=<ID=STDEV_LEN,Description="SV length standard deviation filter"> | ||
##FILTER=<ID=COV_MIN,Description="Minimum coverage filter"> | ||
##FILTER=<ID=COV_CHANGE,Description="Coverage change filter"> | ||
##FILTER=<ID=COV_CHANGE_FRAC,Description="Coverage fractional change filter"> | ||
##FILTER=<ID=MOSAIC_AF,Description="Mosaic maximum allele frequency filter"> | ||
##FILTER=<ID=ALN_NM,Description="Length adjusted mismatch filter"> | ||
##FILTER=<ID=STRAND,Description="Strand support filter"> | ||
##FILTER=<ID=SVLEN_MIN,Description="SV length filter"> | ||
##INFO=<ID=PRECISE,Number=0,Type=Flag,Description="Structural variation with precise breakpoints"> | ||
##INFO=<ID=IMPRECISE,Number=0,Type=Flag,Description="Structural variation with imprecise breakpoints"> | ||
##INFO=<ID=MOSAIC,Number=0,Type=Flag,Description="Structural variation classified as putative mosaic"> | ||
##INFO=<ID=SVLEN,Number=1,Type=Integer,Description="Length of structural variation"> | ||
##INFO=<ID=SVTYPE,Number=1,Type=String,Description="Type of structural variation"> | ||
##INFO=<ID=CHR2,Number=1,Type=String,Description="Mate chromsome for BND SVs"> | ||
##INFO=<ID=SUPPORT,Number=1,Type=Integer,Description="Number of reads supporting the structural variation"> | ||
##INFO=<ID=SUPPORT_INLINE,Number=1,Type=Integer,Description="Number of reads supporting an INS/DEL SV (non-split events only)"> | ||
##INFO=<ID=SUPPORT_LONG,Number=1,Type=Integer,Description="Number of soft-clipped reads putatively supporting the long insertion SV"> | ||
##INFO=<ID=END,Number=1,Type=Integer,Description="End position of structural variation"> | ||
##INFO=<ID=STDEV_POS,Number=1,Type=Float,Description="Standard deviation of structural variation start position"> | ||
##INFO=<ID=STDEV_LEN,Number=1,Type=Float,Description="Standard deviation of structural variation length"> | ||
##INFO=<ID=COVERAGE,Number=.,Type=Float,Description="Coverages near upstream, start, center, end, downstream of structural variation"> | ||
##INFO=<ID=STRAND,Number=1,Type=String,Description="Strands of supporting reads for structural variant"> | ||
##INFO=<ID=AC,Number=.,Type=Integer,Description="Allele count, summed up over all samples"> | ||
##INFO=<ID=SUPP_VEC,Number=1,Type=String,Description="List of read support for all samples"> | ||
##INFO=<ID=CONSENSUS_SUPPORT,Number=1,Type=Integer,Description="Number of reads that support the generated insertion (INS) consensus sequence"> | ||
##INFO=<ID=RNAMES,Number=.,Type=String,Description="Names of supporting reads (if enabled with --output-rnames)"> | ||
##INFO=<ID=AF,Number=1,Type=Float,Description="Allele Frequency"> | ||
##INFO=<ID=NM,Number=.,Type=Float,Description="Mean number of query alignment length adjusted mismatches of supporting reads"> | ||
##INFO=<ID=PHASE,Number=.,Type=String,Description="Phasing information derived from supporting reads, represented as list of: HAPLOTYPE,PHASESET,HAPLOTYPE_SUPPORT,PHASESET_SUPPORT,HAPLOTYPE_FILTER,PHASESET_FILTER"> | ||
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT SAMPLE | ||
chr1 1000 Sniffles2.DEL.CM0 N <DEL> 54 PASS PRECISE;SVTYPE=DEL;SVLEN=-50;END=1049;SUPPORT=26;COVERAGE=41,41,42,41,39;STRAND=+-;AC=4;STDEV_LEN=23.094;STDEV_POS=2.887;SUPP_VEC=11 GT:GQ:DR:DV:ID 1/1:60:0:33:Sniffles2.DEL.3720S0 | ||
chr1 2000 Sniffles2.INS.0M0 N GTCCCTCTGTCTCTGCCAACCAGTTAACCTGCTGCTTCCTGGAGGAAGACAGTCCCTCTGTCCCTCTGTCTCTGCCAACCAGTTAACCTGCTGCTTCCTGGAGGCAGACAGTCCCTCT 56 PASS IMPRECISE;SVTYPE=INS;SVLEN=118;END=2000;SUPPORT=30;COVERAGE=31,30,30,30,30;STRAND=+-;AC=4;STDEV_LEN=0.000;STDEV_POS=0.000;SUPP_VEC=11 GT:GQ:DR:DV:ID 1/1:60:0:24:Sniffles2.INS.5S0 | ||
chr1 3000 Sniffles2.INV.215M0 N <INV> 59 PASS PRECISE;SVTYPE=INV;SVLEN=590;END=3589;SUPPORT=16;COVERAGE=39,19,20,20,40;STRAND=-;AC=2;STDEV_LEN=0.000;STDEV_POS=0.000;SUPP_VEC=11 GT:GQ:DR:DV:ID 0/1:24:27:10:Sniffles2.INV.9A95S0 | ||
chr1 4000 Sniffles2.DUP.2F0M1 N <DUP> 60 PASS PRECISE;SVTYPE=DUP;SVLEN=13584;END=17584;SUPPORT=20;COVERAGE=42,44,70,42,44;STRAND=+-;AC=2;STDEV_LEN=0.000;STDEV_POS=0.000;SUPP_VEC=11 GT:GQ:DR:DV:ID 0/1:60:43:18:Sniffles2.DUP.954CS1 | ||
chr1 5000 Sniffles2.BND.FFM0 N N]chrUn_JTFH01000344v1_decoy:679] 58 PASS PRECISE;SVTYPE=BND;SUPPORT=7;COVERAGE=44,30,42,42,40;STRAND=+-;AC=1;STDEV_LEN=0.000;STDEV_POS=0.000;SUPP_VEC=11 GT:GQ:DR:DV:ID 0/1:15:23:8:Sniffles2.BND.C83CS0 |
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