198c9b8daecc44fbda6a6494c566c723920f030a
lrnassar
  Wed Mar 11 18:25:21 2026 -0700
Fixing a few hundred clear typos with the help of Claude. Some are less important in code comments, but majority of them are in user-facing places. I manually approved 60%+ of the changes and didn't see any that were an incorrect suggestion, at worst it was potentially uncessesary, like a code comment having cant instead of can't. No RM.

diff --git src/hg/makeDb/trackDb/human/longReadVariants.html src/hg/makeDb/trackDb/human/longReadVariants.html
index 630ead4fa43..652de38b9ee 100644
--- src/hg/makeDb/trackDb/human/longReadVariants.html
+++ src/hg/makeDb/trackDb/human/longReadVariants.html
@@ -1,21 +1,21 @@
 <h2>Description</h2>
 <p>
 The tracks listed here contain variants using long-read sequencing technologies.</p>
 <ul>
     <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
+Hover over the feature to see more information, explained on the 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>