50d9c48ac1cbb26bfbbb5e132f69d5391d782f7d
jnavarr5
  Wed Mar 3 08:08:34 2021 -0800
Removing an 's' from deletions, refs #18492

diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html
index 82263fa..9b7e655 100755
--- src/hg/htdocs/goldenPath/newsarch.html
+++ src/hg/htdocs/goldenPath/newsarch.html
@@ -48,31 +48,31 @@
     </div>
   </div> 
 </div>
 
 <!-- ============= 2021 archived news ============= -->
 <a name="2021"></a>
 <a name="030221"></a>
 <h2>Mar. 02, 2021 &nbsp;&nbsp; CADD Scores now available for hg19 and hg38</h2>
 <p>
 We are happy to announce the release of a new track for human assemblies, 
 <a href="../cgi-bin/hgTrackUi?db=hg19&chr=chrX">hg19</a> and
 <a href="../cgi-bin/hgTrackUi?db=hg38&chr=chrX">hg38</a>. The new track shows
 <a href="https://cadd.gs.washington.edu/" target="_blank">Combined Annotation Dependent Depletion
 (CADD)</a> scores for each base in the genome and corresponds to the v1.6 developmental release.
 CADD is a tool for scoring the deleteriousness of single nucleotide variants as well as
-insertion/deletions variants in the human genome. CADD scores strongly correlate with allelic
+insertion/deletion variants in the human genome. CADD scores strongly correlate with allelic
 diversity, pathogenicity of both coding and non-coding variants, experimentally measured regulatory
 effects, and also highly rank causal variants within individual genome sequences. Finally, CADD
 scores of complex trait-associated variants from genome-wide association studies (GWAS) are
 significantly higher than matched controls and correlate with study sample size, likely reflecting
 the increased accuracy of larger GWAS.</p>
 
 <p>The supertrack consists of the following tracks:</p>
 <ul>
   <li><strong>CADD</strong> (composite track)
     <ul>
       <li>Mutation: A</li>
       <li>Mutation: C</li>
       <li>Mutation: G</li>
       <li>Mutation: T</li>
     </ul>