bac95a147f49cd331052e597006e04b3deee40fc max Wed Apr 22 10:43:20 2026 -0700 lrSv/srSv: human-readable SV type filter labels, script cleanups Add human-readable labels to the supertrack-level svType filter on both the lrSv and srSv supertracks using the "CODE|CODE (Long name)" filterValues syntax: DEL -> "DEL (Deletion)", INS -> "INS (Insertion)", etc. Labels keep the short code up front so users can match what hgTracks shows next to each feature. Also sweep in the in-progress converter/as-file cleanups under scripts/lrSv/ and scripts/srSv/ (introduction of lrSvCommon.py helpers, consistent insLen / svLen / AC column naming, tightened field-description text) that had been piling up as an unstaged working tree. refs #36258 diff --git src/hg/makeDb/scripts/lrSv/lrSvGustafson.as src/hg/makeDb/scripts/lrSv/lrSvGustafson.as index 4196e8f9bf9..6284c533e81 100644 --- src/hg/makeDb/scripts/lrSv/lrSvGustafson.as +++ src/hg/makeDb/scripts/lrSv/lrSvGustafson.as @@ -1,19 +1,21 @@ table lrSvGustafson "Gustafson 2024 1000 Genomes ONT long-read structural variants (100 samples)" ( string chrom; "Chromosome" uint chromStart; "Start position" uint chromEnd; "End position" string name; "Variant ID" uint score; "Score" char[1] strand; "Strand" uint thickStart; "Thick start (same as chromStart)" uint thickEnd; "Thick end (same as chromEnd)" uint reserved; "Item color" string svType; "SV Type|DEL, INS, DUP or INV" - int svLen; "SV Length|Absolute length of the SV in base pairs" + int svLen; "SV Length|Length of the variant on the reference in base pairs" + int insLen; "Insertion Length|Length of inserted sequence, 0 for DEL/INV/CPX" + int AC; "Allele Count|Placeholder (2 * sampleCount); Gustafson callset is site-level" uint sampleCount; "Sample Count|Number of samples carrying this variant (SUPP)" uint varCalls; "Caller Support|Number of per-caller calls supporting this variant" uint precise; "Precise Boundaries|1 if the source caller flagged this variant PRECISE" string strands; "Strands|Strand orientation from the source caller" )