65091fe6f6487c23d650a144e947fc1c582d3f40 max Tue Apr 21 02:16:16 2026 -0700 abelSv: move under lrSv supertrack as short-read comparison subtrack Move the Abel et al. 2020 CCDG 17,795-genome SV callset from a top-level hg38 track to a subtrack of the lrSv supertrack (parallel to onekg3202Sr) and relabel shortLabel/longLabel to flag Illumina short-read provenance. The same bigBed is now visible on hg38 in the long-read SV browsing context. Also: - Clarify abelSv.html variant counts: 738,624 upstream unique SVs across both callsets, 737,998 after B37->hg38 liftOver (626 unmapped). B38=458,106, B37lift=279,892. - lrSv.html: fix triple-slash https:/// in the Ebert et al. Science reference URL. - bigBed.html: add closing on the extra-fields pipe-separator bullet and tighten a comma in the same sentence. refs #36258, refs #37376 diff --git src/hg/makeDb/trackDb/human/lrSv.ra src/hg/makeDb/trackDb/human/lrSv.ra index f51bf6bfca1..808454bdf4b 100644 --- src/hg/makeDb/trackDb/human/lrSv.ra +++ src/hg/makeDb/trackDb/human/lrSv.ra @@ -43,30 +43,69 @@ filterType.insType multipleListOr filterLabel.insType Insertion/Deletion Type filterValues.family Alu,HERVK,L1,LTR5_Hs,SVA filterType.family multipleListOr filterLabel.family Transposon Family filterByRange.svLen on filterLabel.svLen SV Length filterByRange.alleleFreq on filterLimits.alleleFreq 0:1 filterLabel.alleleFreq Allele Frequency filterByRange.alleleCount on filterLabel.alleleCount Allele Count skipEmptyFields on priority 2 + track abelSv + parent lrSv + bigDataUrl /gbdb/$D/abelSv/abelSv.bb + shortLabel CCDG 17795 SR SVs + longLabel Structural Variants from 17,795 Genomes - Illumina SHORT-READ CCDG callset (Abel et al. 2020) - included for comparison + type bigBed 9 + + itemRgb on + visibility dense + mouseOver $name ($svType) len=$svLength AF=$af AC=$ac/$an callset=$callset MSQ=$msq + skipEmptyFields on + skipFields mateChrom,matePos + filterValues.svType DEL|deletion,DUP|duplication,INV|inversion,MEI|mobile element insertion,BND|breakend/translocation + filterType.svType multipleListOr + filterLabel.svType SV Type + filterValues.callset B38|Native GRCh38 callset (14623 samples),B37lift|Lifted from GRCh37 callset (8417 samples) + filterType.callset multipleListOr + filterLabel.callset Source Callset + filterValues.filter PASS|High confidence,LOW|Low confidence + filterType.filter multipleListOr + filterLabel.filter Filter Status + filterByRange.af on + filter.af 0:1 + filterLimits.af 0:1 + filterLabel.af Allele Frequency (AF) + filterByRange.svLength on + filter.svLength 0:250000000 + filterLimits.svLength -1:250000000 + filterLabel.svLength SV Length (bp; -1 for BND) + filterByRange.msq on + filter.msq 0:500 + filterLimits.msq 0:500 + filterLabel.msq Mean Sample Quality (MSQ) + filterByRange.ac on + filter.ac 0:30000 + filterLimits.ac 0:30000 + filterLabel.ac Allele Count (AC) + url https://www.nature.com/articles/s41586-020-2371-0 + urlLabel Abel et al, Nature 2020: + track onekg3202Sr parent lrSv bigDataUrl /gbdb/$D/lrSv/onekg3202sr.bb shortLabel 1KG 3202 SR SVs longLabel 1000 Genomes 3202-sample Illumina SHORT-READ GATK-SV callset (Byrska-Bishop 2022) - included for comparison type bigBed 9 + itemRgb on visibility dense mouseOver $name ($svType) len=$svLen AF=$alleleFreq AC=$alleleCount/$alleleNumber popMax=$popmaxAf filterValues.svType DEL,INS,DUP,INV,CPX,CTX,CNV filterType.svType multipleListOr filterLabel.svType SV Type filter.svLen 0:154807729 filterByRange.svLen on filterLabel.svLen SV Length