f09028646c6429d692a80cc38d214e805724e7fa lrnassar Sat Jun 13 10:51:38 2026 -0700 lrSv: default all subtracks to hide except lrSvAll (pack), add lrSvAll desc page. refs #36258 Set the 15 released lrSv subtracks to "visibility hide" so the supertrack opens with only the merged overview visible; lrSvAll stays "visibility pack". Add the missing lrSvAll.html description page (Description, Display Conventions, Methods, Data Access, Credits) describing the position-merged combined track. diff --git src/hg/makeDb/trackDb/human/lrSvAll.html src/hg/makeDb/trackDb/human/lrSvAll.html new file mode 100644 index 00000000000..29ef4d56918 --- /dev/null +++ src/hg/makeDb/trackDb/human/lrSvAll.html @@ -0,0 +1,81 @@ +

Description

+

+This track combines the structural-variant (SV) callsets from the individual +subtracks of the Long-read SVs supertrack into a +single, position-merged overview. Each item is an SV locus seen in one or more +of the contributing long-read databases. For every merged locus the track +records which databases report it, the summed allele count across those +databases, and the range of allele frequencies observed, making it useful for +quickly seeing how widely an SV has been reported across cohorts. +

+

+This is a summary view. For cohort-specific genotypes, per-population allele +frequencies, and dataset-specific annotations, use the individual subtracks of +the supertrack. The merge includes the released long-read callsets only; +preliminary or unpublished subtracks (e.g. the Kim PD brain, 1000 Genomes +linear, and HPRC Jasmine sets) are not part of this merged track. +

+ +

Display Conventions and Configuration

+

+Items are colored by SV type, matching the individual subtracks: +

+

+

+The mouseover shows the variant name, SV type, reference and insertion lengths, +the list of contributing source databases, the allele-frequency range across +those databases, and the total allele count. Filters are available for the +source database, SV type, SV length, insertion +length, total allele count, minimum and maximum allele +frequency, and the number of source databases reporting each locus. +The detail page lists the per-database allele counts. +

+ +

Methods

+

+The merged track is built by the lrSvMergeAll.py script, which reads +the bigBed of each contributing subtrack (configured in +databases.tsv) and groups records that share an identical +(chromosome, start, end) position and SV type. For each merged locus +the script records the set of contributing databases (sources), the +number of those databases (sourceCount), the sum of their allele counts +(AC), and the minimum and maximum allele frequency across databases +that report one (minAF, maxAF). The per-database allele counts +are carried as additional columns. +

+

+The step-by-step build commands are recorded in the UCSC makeDoc for this track +collection: + +doc/hg38/lrSv.txt. The merge script and autoSql schema live in + +makeDb/scripts/lrSv. +

+ +

Data Access

+

+The data can be explored interactively with the +Table Browser or the +Data Integrator, and accessed +programmatically through our API, +track=lrSvAll. +

+

+The bigBed is available from +our +download server as lrSvAll.bb. Example: +bigBedToBed http://hgdownload.soe.ucsc.edu/gbdb/$db/lrSv/lrSvAll.bb -chrom=chr21 -start=0 -end=100000000 stdout. +

+ +

Credits

+

+This merged view is derived entirely from the contributing long-read SV +callsets; please see the individual subtrack description pages for the data +producers and citations for each cohort. +