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/cnpRedon.html src/hg/makeDb/trackDb/human/hg18/cnpRedon.html
index 7c641f638b2..8ceab130a0b 100644
--- src/hg/makeDb/trackDb/human/hg18/cnpRedon.html
+++ src/hg/makeDb/trackDb/human/hg18/cnpRedon.html
@@ -20,28 +20,28 @@
 <LI>
 <B><FONT COLOR="gray">Gray</FONT>:</B> gain or loss (unknown direction)
 </UL></P>
 
 <H2>Methods</H2>
 
 <P>Experiments were performed with the International HapMap DNA and cell-line collection
 using two technologies: comparative analysis of hybridization intensities on
 Affymetric GeneChip Human Mapping 500K early access arrays (500K EA)
 and comparative genomic hybridization with a Whole Genome TilePath (WGTP)
 array.
 
 <H2>Validation</H2>
 
 
-The authors utilized numerous quality meaures, including
+The authors utilized numerous quality measures, including
 repeated experiments on the WGTP for 82 individual and on the 500K EA for 15 individuals.
 The average false-positive rate per experiment was held beneath 5%.  Aberrant chromosomes were
 removed from the analysis.    Further details are available in the Nature paper cited below.
 
 <H2>References</H2>
 
 <P>
 Redon, R., Ishikawa, S., Fitch, K., Feuk, L., Perry, G., Andrews, T., Fiegler, H.,
 Lee, C., Jones, K., Scherer, S., Hurles, M. <em>et al</em>.
 <A HREF="https://www.nature.com/articles/nature05329" TARGET=_blank>
 Global variation in copy number in the human genome</A>.
 <em>Nature</em> <B>444</B>(7118), 444-454 (2006).