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/hg18/cnp.html src/hg/makeDb/trackDb/human/hg18/cnp.html
index b75f4614a38..1f6a2657ac1 100644
--- src/hg/makeDb/trackDb/human/hg18/cnp.html
+++ src/hg/makeDb/trackDb/human/hg18/cnp.html
@@ -232,31 +232,31 @@
 matched prediction across a set of 12-24 individuals. The authors confirmed 51
 of 60 candidate variants by this criterion.
 </P>
 <P>
 The authors performed quantitative PCR in all 269 HapMap DNA samples for 11
 candidate deletions that overlapped the coding exons of genes and that were
 discovered in many individuals. At 10/11 loci, the authors observed three
 discrete clusters, identifying individuals with zero, one and two gene copies.
 All 60 trios displayed Mendelian inheritance for the ten deletions, as well as
 Hardy-Weinberg equilibrium in all four populations surveyed, and transmission
 rates close to 50%. This suggests that the deletions behave as a stable,
 heritable genetic polymorphism.
 </P>
 
 <H3>Redon analysis of HapMap data</H3>
-The authors utilized numerous quality meaures, including repeated experiments
+The authors utilized numerous quality measures, including repeated experiments
 on the WGTP array for 82 individuals and on the 500K EA array for 15
 individuals. The average false-positive rate per experiment was held beneath
 5%. Aberrant chromosomes were removed from the analysis.    
 </P>
 
 <H2>Credits</H2>
 <P>
 Thanks to Lars Feuk at <A HREF="https://www.sickkids.ca/" TARGET=_blank>The
 Hospital for Sick Children in Toronto</A> for providing these data in hg18
 coordinates.
 </P>
 
 
 <H2>References</H2>
 <P>