29c46a47cbb40f44c06103e8294e8864d82256a7
max
  Mon Aug 17 05:56:59 2026 -0700
lrSv: fix typos and HTML consistency in track description pages

GitHub capitalization, Continuous, missing article/period in HPRC2 row, 1000 Genomes capitalization, quote target/id attributes

diff --git src/hg/makeDb/trackDb/human/lrSv.html src/hg/makeDb/trackDb/human/lrSv.html
index e4eb02ad191..67ddadc1626 100644
--- src/hg/makeDb/trackDb/human/lrSv.html
+++ src/hg/makeDb/trackDb/human/lrSv.html
@@ -1,25 +1,25 @@
 <h2>Description</h2>
 <p>
 This track collection contains structural variant (SV) calls derived from long-read sequencing
 studies. Structural variants are genomic rearrangements larger than ~50 bp, including
 deletions, insertions, duplications, inversions, and translocations. Long-read sequencing
 technologies can span repetitive regions and resolve complex rearrangements
 that are difficult to detect with short-read methods.
 The long read datasets described below were produced with one of two sequencing technologies, Oxford Nanopore
 Technologies (ONT) or Pacific Biosciences (PacBio, whose highly accurate reads are also called
-HiFi, unlike the longer but less accurate CLR, Continous Long-Reads). </p>
+HiFi, unlike the longer but less accurate CLR, Continuous Long-Reads). </p>
 
 <h3>Available Datasets</h3>
 <p>
 SV length statistics (min / median / max) use the size of the variant in base
 pairs: the inserted-sequence length for insertions and the reference span for
 deletions and other types. (For insertions the <tt>svLen</tt> reference-span
 field is only a 1-2 bp placeholder, so the inserted length is reported
 instead.) Some tracks include sites of length 0, complex events where the
 reference and alternate alleles differ in sequence but not in length.
 For example, two different insertions, one in either sequence, is usually
 called a "complex" event.
 </p>
 <!-- <p>
 For short-read structural-variant comparators (CCDG 17,795, 1KG 3202,
 ToMMo 48K CNV) see the companion
@@ -238,36 +238,36 @@
   <td>Cystic fibrosis (CF) patients from the CF Canada-Sick Kids Program in Individual CF Therapy (CFIT). Long-read WGS used for GWAS LD fine-mapping</td>
   <td>Yes (all CF)</td>
   <td>~50x PacBio CLR (34, Sequel I) + ~76x HiFi (67, Sequel II)</td>
   <td>87,068</td>
   <td>4</td>
   <td>160</td>
   <td>1,321,484</td>
 </tr>
 </table>
 
 <p>
 Note: there is likely some overlap in sample composition across these collections.
 For example, 1000 Genomes samples are also included in HPRC and CoLoRSdb.
 </p>
 
-<h3 id='1000genomes'>1000 Genomes long-read callsets</h3>
+<h3 id="1000genomes">1000 Genomes long-read callsets</h3>
 <p>
 Several of the datasets above are long-read callsets on the 1000 Genomes
 Project samples, produced by different groups with different technologies and
 variant-calling strategies. The
-<a href="hgTrackUi?g=lrSv1kLin">1KG Lin merged</a> track combines these and added more 1000 genomes assemblies for a
+<a href="hgTrackUi?g=lrSv1kLin">1KG Lin merged</a> track combines these and added more 1000 Genomes assemblies for a
 single 1,218-individual callset (Lin et al., submitted). The table below
 summarizes all callsets obtained from 1000 Genomes samples.
 </p>
 <table class="stdTbl">
 <tr>
   <th>Callset</th>
   <th>N samples</th>
   <th>Study</th>
   <th>Data source</th>
   <th>Variant calling</th>
   <th>UCSC track</th>
 </tr>
 <tr>
   <td>Lin_1218</td>
   <td>1,218</td>
@@ -292,31 +292,31 @@
   <td>Linear-reference-based</td>
   <td><a href="hgTrackUi?g=gustafsonSv">1KG UW ONT</a></td>
 </tr>
 <tr>
   <td>Boehringer ONT 888</td>
   <td>888</td>
   <td>Noyvert et al., Imputation of structural variants using a multi-ancestry long-read sequencing panel enables identification of disease associations</td>
   <td>Oxford Nanopore long reads (5 ancestry groups)</td>
   <td>Sniffles2</td>
   <td><a href="hgTrackUi?g=noyvertSv">1KG Boehringer ONT 888</a></td>
 </tr>
 <tr>
   <td>HPRC2 Minigraph-Cactus</td>
   <td>232</td>
   <td>Lucas et al., HPRC2: a human pangenome reference with near-complete coverage of common genetic variation</td>
-  <td>Near-T2T assembly (30x-60x HiFi+ONT), <a target=_blank href="https://github.com/wwliao/hprc_release2_variant_calling">a linear callset</a> was included for Lin et al merge. </td>
+  <td>Near-T2T assembly (30x-60x HiFi+ONT), <a target="_blank" href="https://github.com/wwliao/hprc_release2_variant_calling">a linear callset</a> was included for the Lin et al. merge. </td>
   <td>Minigraph-cactus graph</td>
   <td><a href="hgTrackUi?g=hprc2v21Sv">HPRC v2.1</a></td>
 </tr>
 <tr>
   <td>HGSVC3</td>
   <td>65</td>
   <td>Logsdon et al., Complex genetic variation in nearly complete human genomes</td>
   <td>Near-T2T assembly (37-40x HiFi+ONT)</td>
   <td>Linear-reference-based</td>
   <td><a href="hgTrackUi?g=hgsvc3Sv">HGSVC3</a></td>
 </tr>
 </table>
 
 <h3><a href="hgTrackUi?g=colorsDbSv">CoLoRSdb SVs</a></h3>
 <p>