da9a225ac1d17c6c6659209c0dfb4534e6ab51d7
jnavarr5
  Tue Sep 30 16:16:07 2025 -0700
Fixing a typo in CoLoRSdb (missing S). Bolding the track names. Using lowercase s in 'small' and 'structural', refs #34120

diff --git src/hg/makeDb/trackDb/human/longReadVariants.html src/hg/makeDb/trackDb/human/longReadVariants.html
index 703efc0c8a4..630ead4fa43 100644
--- src/hg/makeDb/trackDb/human/longReadVariants.html
+++ src/hg/makeDb/trackDb/human/longReadVariants.html
@@ -1,19 +1,21 @@
 <h2>Description</h2>
 <p>
 The tracks listed here contain variants using long-read sequencing technologies.</p>
 <ul>
-    <li>CoLoRSdb Small variants: small genetic variants (single nucleotide polymorphisms and short
-        insertions and deletions) called with DeepVariant and merged with GLnexus/bcftools.</li>
-    <li>CoLoRdb Structural variants: structural variants (insertions, deletions, and inversions)
-        discovered with pbsv and merged across samples using Jasmine.</li>
+    <li>
+      <b>CoLoRSdb small variants:</b> small genetic variants (single nucleotide polymorphisms and
+      short insertions and deletions) called with DeepVariant and merged with GLnexus/bcftools.</li>
+    <li>
+      <b>CoLoRSdb structural variants:</b> structural variants (insertions, deletions, and
+      inversions) discovered with pbsv and merged across samples using Jasmine.</li>
 </ul>
 
 <h2>Display conventions</h2>
 <p>
 Hover over the feature to see more information, explained on teh track details page of the
 particular track or when clicking onto the feature.</p>
 
 <h2>Credits</h2>
 <p>
 For data provenance, access and descriptions, please click the documentation via the link above.
 </p>