9a63ecfed718d4ad0b2c5212c7ad8844c9d23531
lrnassar
  Mon Jun 29 14:21:07 2026 -0700
lrSv: add GitHub source links (makedoc, scripts, trackDb.ra) to all description pages. refs #36258

Per the updated qa-track standard, link the track's UCSC source artifacts on
github.com/ucscGenomeBrowser/kent from every lrSv description page:
- Add the missing links to the lrSv supertrack page and colorsDbSv.
- Backfill the trackDb.ra link (third artifact) across the subtrack pages that
already linked the makedoc + scripts dir.
lrSv1kLin is left as its placeholder (staged, not released).

diff --git src/hg/makeDb/trackDb/human/chirmade101Sv.html src/hg/makeDb/trackDb/human/chirmade101Sv.html
index dc35b075c66..5f9b2a575e6 100644
--- src/hg/makeDb/trackDb/human/chirmade101Sv.html
+++ src/hg/makeDb/trackDb/human/chirmade101Sv.html
@@ -1,120 +1,120 @@
 <h2>Description</h2>
 <p>
 This track shows structural variants (SVs) identified by long-read
 whole-genome sequencing of 101 individuals, released together with the
 <a href="https://svatalog.research.sickkids.ca/" target="_blank">GWAS SVatalog</a>
 web tool described in Chirmade et al. 2026. GWAS SVatalog computes and
 visualizes linkage disequilibrium between these SVs and GWAS-associated
 SNPs so that investigators can assess whether a SNP association signal
 may be tagging an underlying SV.
 </p>
 <p>
 The table contains 87,068 SVs (42,435 deletions, 41,619 insertions,
 1,394 duplications, 912 inversions, 708 complex events; byte-identical
 duplicate records have been removed). Each SV is
 annotated with gene overlaps, GC content, repeat context, ClinGen
 haploinsufficiency / triplosensitivity scores, gnomAD per-gene constraint
 metrics (pLI, LOEUF, missense O/E), OMIM phenotype associations, ClinVar
 variant IDs, and overlaps with DGV, Decipher and ClinGen regional
 annotations.
 </p>
 
 <h2>Display Conventions and Configuration</h2>
 <p>
 Items are colored by SV type:
 <ul>
 <li><span style="color: rgb(200,0,0);">Deletions (del)</span> - red</li>
 <li><span style="color: rgb(0,0,200);">Insertions (ins)</span> - blue</li>
 <li><span style="color: rgb(0,160,0);">Duplications (dup)</span> - green</li>
 <li><span style="color: rgb(230,140,0);">Inversions (inv)</span> - orange</li>
 <li><span style="color: rgb(140,0,200);">Complex</span> - purple</li>
 </ul>
 </p>
 <p>
 Filters are available for SV type, SV length and the number of overlapping
 genes. The detail page shows the full annotation row: gene-level constraint
 scores (per overlapping gene), ClinGen / Decipher / ClinVar region matches,
 OMIM phenotype annotations and gnomAD SV frequencies at &gt;=90% reciprocal
 overlap. Because most genomic regions carry no clinical annotation, many
 columns will be blank for an arbitrary SV.
 </p>
 
 <h2>Methods</h2>
 <p>
 Chirmade et al. 2026 called SVs from 101 whole-genome sequenced individuals
 enrolled in the CF Canada-SickKids Program in Individualized Therapy
 (CFIT), a predominantly-European cohort of people with cystic fibrosis.
 Each sample was sequenced with two long-read / linked-read technologies:
 PacBio continuous long reads on Sequel I (34 samples, 50x) or Sequel II
 (67 samples, 76x), and 10X Genomics linked reads on Illumina HiSeq X at
 ~30x. SVs were called per sample with pbsv v2.2.2 (pbmm2 alignments) and
 Sniffles v1.0.11 (NGMLR alignments) on the PacBio CLR data, and with Long
 Ranger, CNVnator v0.4, ERDS v1.1 and Manta v1.6.0 on the 10XG data.
 Per-platform and cross-platform calls were merged in three steps using a
 50% reciprocal overlap rule (pbsv anchored, tagged by Sniffles on PacBio;
 Manta anchored, augmented by CNVnator, ERDS and Long Ranger deletions on
 10XG; then a cross-platform merge with PacBio coordinates preferred), and
 SV records present in fewer than three participants were dropped. The
 released catalog contains 87,183 SVs (42,435 deletions, 41,734 insertions,
 1,394 duplications, 912 inversions and 708 complex events); the
 pre-computed GWAS SVatalog LD analyses use a common-SV subset of 35,732
 sites against 116,870 GWAS-Catalog SNPs.
 </p>
 <p>
 The annotation TSV <tt>sv_annotations.tsv</tt> was downloaded from the
 Zenodo companion record,
 <a href="https://zenodo.org/records/13367574" target="_blank">
 zenodo.org/records/13367574</a>. Coordinates in the TSV are 1-based closed
 and were converted to 0-based half-open BED for this track.
 </p>
 <p>
 The step-by-step build commands (download, coordinate shift, format
 conversion, bigBed build) are recorded in the UCSC makeDoc for this track
 container:
 <a href="https://github.com/ucscGenomeBrowser/kent/blob/master/src/hg/makeDb/doc/hg38/lrSv.txt" target="_blank">
 doc/hg38/lrSv.txt</a>. The conversion scripts and autoSql schemas live in
 <a href="https://github.com/ucscGenomeBrowser/kent/tree/master/src/hg/makeDb/scripts/lrSv" target="_blank">
-makeDb/scripts/lrSv</a>.
+makeDb/scripts/lrSv</a>, and the track configuration is in <a href="https://github.com/ucscGenomeBrowser/kent/blob/master/src/hg/makeDb/trackDb/human/lrSv.ra" target="_blank">trackDb/human/lrSv.ra</a>.
 </p>
 
 <h2>Data Access</h2>
 <p>
 The data can be explored interactively in table format with the
 <a href="../cgi-bin/hgTables">Table Browser</a> or the
 <a href="../cgi-bin/hgIntegrator">Data Integrator</a>, and accessed
 programmatically through our <a href="https://api.genome.ucsc.edu">API</a>,
 track=<i>chirmade101Sv</i>.
 </p>
 <p>
 The bigBed is available from
 <a href="http://hgdownload.soe.ucsc.edu/gbdb/hg38/lrSv/" target="_blank">our
 download server</a> as <tt>chirmade101.bb</tt>. Example:
 <tt>bigBedToBed http://hgdownload.soe.ucsc.edu/gbdb/hg38/lrSv/chirmade101.bb -chrom=chr21 -start=0 -end=100000000 stdout</tt>.
 </p>
 <p>
 The original annotation table is available on Zenodo:
 <a href="https://zenodo.org/records/13367574" target="_blank">zenodo.org/records/13367574</a>.
 The GWAS SVatalog web tool itself is at
 <a href="https://svatalog.research.sickkids.ca/" target="_blank">svatalog.research.sickkids.ca</a>.
 </p>
 
 <h2>Credits</h2>
 <p>
 Thanks to Chirmade, Strug and colleagues at The Hospital for Sick Children
 and the University of Toronto for releasing this annotated long-read SV
 callset alongside the GWAS SVatalog tool.
 </p>
 
 <h2>References</h2>
 
 
 <p>
 Chirmade S, Wang Z, Mastromatteo S, Sanders E, Thiruvahindrapuram B, Nalpathamkalam T, Pellecchia G,
 Lin F, Keenan K, Patel RV <em>et al</em>.
 <a href="https://doi.org/10.1038/s41437-025-00809-2" target="_blank">
 GWAS SVatalog: a visualization tool to aid fine-mapping of GWAS loci with structural variations</a>.
 <em>Heredity (Edinb)</em>. 2026 Mar;135(3):199-210.
 PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/41203876" target="_blank">41203876</a>; PMC: <a
 href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13031531/" target="_blank">PMC13031531</a>
 </p>