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/dbSnp155Composite.html src/hg/makeDb/trackDb/human/dbSnp155Composite.html
index 0dd59a48626..276dbf0738e 100644
--- src/hg/makeDb/trackDb/human/dbSnp155Composite.html
+++ src/hg/makeDb/trackDb/human/dbSnp155Composite.html
@@ -512,31 +512,31 @@
 We downloaded JSON files available from dbSNP at
 <a href="https://ftp.ncbi.nlm.nih.gov/snp/archive/b155/JSON/"
 target=_blank>https://ftp.ncbi.nlm.nih.gov/snp/archive/b155/JSON/</a>,
 extracted a subset of the information about each variant, and collated
 it into a bigBed file using the
 <a href="https://github.com/ucscGenomeBrowser/kent/blob/master/src/hg/lib/bigDbSnp.as"
 target=_blank>bigDbSnp.as</a> schema with the information
 necessary for filtering and displaying the variants,
 as well as a separate file containing more detailed information to be
 displayed on each variant's details page
 (<a href="https://github.com/ucscGenomeBrowser/kent/blob/master/src/hg/lib/dbSnpDetails.as"
 target=_blank>dbSnpDetails.as</a> schema).
 
 <h2>Data Access</h2>
 <p>
-<b>Note:</b> It is not recommeneded to use LiftOver to convert SNPs between assemblies,
+<b>Note:</b> It is not recommended to use LiftOver to convert SNPs between assemblies,
 and more information about how to convert SNPs between assemblies can be found on the following
 <a href="/FAQ/FAQreleases.html#snpConversion">FAQ entry</a>.</p>
 <p>
 Since dbSNP has grown to include over 1 billion variants, the size of the All dbSNP (155)
 subtrack can cause the
 <a href="../../cgi-bin/hgTables" target=_blank>Table Browser</a> and
 <a href="../../cgi-bin/hgIntegrator" target=_blank>Data Integrator</a>
 to time out, leading to a blank page or truncated output,
 unless queries are restricted to a chromosomal region, to particular defined regions, to a specific set 
 of rs# IDs (which can be pasted/uploaded into the Table Browser),
 or to one of the subset tracks such as Common (~15 million variants) or ClinVar (~0.8M variants).
 </p><p>
 For automated analysis, the track data files can be downloaded from the downloads server for
 <a href="http://hgdownload.soe.ucsc.edu/gbdb/hg19/snp/" target=_blank>hg19</a> and
 <a href="http://hgdownload.soe.ucsc.edu/gbdb/hg38/snp/" target=_blank>hg38</a>.