0bd565e053abc8c74475f352bedfd37e41312fd2
max
Wed Aug 12 02:15:40 2026 -0700
lrSv: update noyvertSv docs and align merged-track source labels, refs #37888
Follow-up to author (Boris Noyvert) feedback on the Noyvert/Boehringer
long-read SV dataset.
noyvertSv.html:
- restore neutral wording about the shared 1000G ONT reads; drop the
"independent reprocessing" phrasing and the call-level overlap
interpretation the authors objected to
- note that singletons (SVs in a single sample) were excluded, so the
panel is not exhaustive for the rarest variants
- add the medRxiv preprint link alongside the eLife reference
Give each dataset one consistent name across its subtrack and the merged
(lrSvAll) source filter (databases.tsv + lrSvAll.ra + lrSv.ra):
Noyvert 888 (1000G ONT) -> 1KG ONT Boehringer 888
1KG ONT Vienna 1,019 -> 1KG ONT 1019
1KG ONT 100 (Gustafson) -> 1KG ONT UW 100
The gustafsonSv subtrack short/long labels read 97 samples; the paper and
our track docs report 100 (Gustafson et al. 2024, PMID 39358015), so those
are corrected to 100 as well.
Rebuilt lrSvAll.bb with lrSvMergeAll.py; item count unchanged (2,582,278).
diff --git src/hg/makeDb/trackDb/human/lrSvAll.ra src/hg/makeDb/trackDb/human/lrSvAll.ra
index c07bbf83beb..8c4e3e6627d 100644
--- src/hg/makeDb/trackDb/human/lrSvAll.ra
+++ src/hg/makeDb/trackDb/human/lrSvAll.ra
@@ -1,28 +1,28 @@
# AUTO-GENERATED by ~/kent/src/hg/makeDb/scripts/lrSv/lrSvMergeAll.py
# Do not edit by hand - re-run the merge script and re-commit.
track lrSvAll
parent longReadVariants
bigDataUrl /gbdb/$D/lrSv/lrSvAll.bb
shortLabel All LR SVs merged
longLabel All long-read SVs merged across subtracks by exact position, with per-database AC
type bigBed 9 +
itemRgb on
visibility pack
mouseOver Var: $name ($svType)
SV len: $svLen
Ins len: $insLen
Sources: $sources
AF range: $minAF-$maxAF
AC: $AC
- filterValues.sources CoLoRSdb|CoLoRSdb 1427 (PacBio),1000G-ONT-Vienna|1KG ONT Vienna 1019,1000G-ONT|1KG ONT 100 (Gustafson),AoU1K|All of Us 1027 (PacBio),Han945|Han Chinese 945,TommoJapan|ToMMo 333 (Japanese),GA4K|GA4K 502 (rare disease),deCODE|deCODE 3622 (Icelandic),HPRCv2.1|HPRC v2.1 233,HGSVC2|HGSVC2 32,HGSVC3|HGSVC3 65,ArabUAE53|Arab APR 53,China58|CPC 58 (Chinese),Svatalog101|SVatalog 101,CARD|NIH CARD 351 (brain),Noyvert888|Noyvert 888 (1000G ONT)
+ filterValues.sources CoLoRSdb|CoLoRSdb 1427 (PacBio),1000G-ONT-Vienna|1KG ONT 1019,1000G-ONT|1KG ONT UW 100,AoU1K|All of Us 1027 (PacBio),Han945|Han Chinese 945,TommoJapan|ToMMo 333 (Japanese),GA4K|GA4K 502 (rare disease),deCODE|deCODE 3622 (Icelandic),HPRCv2.1|HPRC v2.1 233,HGSVC2|HGSVC2 32,HGSVC3|HGSVC3 65,ArabUAE53|Arab APR 53,China58|CPC 58 (Chinese),Svatalog101|SVatalog 101,CARD|NIH CARD 351 (brain),Noyvert888|1KG ONT Boehringer 888
filterType.sources multipleListOr
filterLabel.sources Source Database
filterValues.svType DEL,INS,DUP,INV,CPX,MIXED,INSDEL,TRA,BND
filterType.svType multipleListOr
filterLabel.svType SV Type
filter.svLen 0:30000000
filterByRange.svLen on
filterLabel.svLen SV Length (bp)
filter.insLen 0:600000
filterByRange.insLen on
filterLabel.insLen Insertion Length (bp)
filter.maxAF 0:1
filterByRange.maxAF on
filterLimits.maxAF 0:1
filterLabel.maxAF Max Allele Frequency (across DBs)