c551260410980f8ab037a8cd7fcf9ee1467bc001
katrina
  Wed Oct 22 15:47:07 2014 -0700
fixing typo in dbSNP announcement: assembies to assemblies
diff --git src/hg/htdocs/indexNews.html src/hg/htdocs/indexNews.html
index 255c2af..a5bd31b 100755
--- src/hg/htdocs/indexNews.html
+++ src/hg/htdocs/indexNews.html
@@ -31,31 +31,31 @@
           training seminars by email, subscribe to the
           <A HREF="http://groups.google.com/a/soe.ucsc.edu/group/genome-announce?hl=en"
           TARGET=_blank>genome-announce</A> mailing list. Please see our
           <a href="http://genome.ucsc.edu/blog"
           target=_blank>blog</a> for posts about Genome Browser tools, features, projects and more.
           </p>
 
     <!-- start news -->
 	<hr>
         <p>
         <font face="courier" size="3"><b>20 October 2014 -
         dbSNP 141 Available for hg19 and hg38</b></font>
         <p>
         We are pleased to announce the release of four tracks derived from NCBI
         <a href="http://www.ncbi.nlm.nih.gov/SNP/" target="_blank">dbSNP</a> Build 141
-        data, available on the two most recent human assembies GRCh37/hg19 and GRCh38/hg38.
+        data, available on the two most recent human assemblies GRCh37/hg19 and GRCh38/hg38.
 	The new tracks contain additional annotation data not included in previous dbSNP
         tracks, with corresponding coloring and filtering options in the Genome Browser.
 	</p>
 	<p>
 	There are three SNP tracks available for the GRCh37/hg19 assembly. One is a track
         containing all mappings of reference SNPs to the human assembly, labeled
         "All SNPs (141)". The other two tracks are subsets of this track and show
         interesting and easily defined subsets of dbSNP:
         </p>
         <ul>
         <li>Common SNPs (141): uniquely mapped variants that appear in at least 1%
         of the population or are 100% non-reference
         <li>Flagged SNPs (141): uniquely mapped variants, excluding Common SNPs,
         that have been flagged by dbSNP as "clinically associated"
         </ul>
@@ -97,31 +97,31 @@
         target="_blank">2014 Ebola Epidemic</a>.
         </p>
         <p>
         If you have a suggestion for a blog post topic, please let us know via our
         <a href="/cgi-bin/hgUserSuggestion">suggestion box</a>.
         </p>
 
         <hr>
         <!-- staged for archive use.  NOTE: condense header line from .... </b></font><p> to </b>: </font>
 
 	<p>
         <font face="courier" size="3"><b>20 October 2014 -
         dbSNP 141 Available for hg19 and hg38</b>: </font>
         We are pleased to announce the release of four tracks derived from NCBI
         <a href="http://www.ncbi.nlm.nih.gov/SNP/" target="_blank">dbSNP</a> Build 141
-        data, available on the two most recent human assembies GRCh37/hg19 and GRCh38/hg38.
+        data, available on the two most recent human assemblies GRCh37/hg19 and GRCh38/hg38.
         <a href="goldenPath/newsarch.html#102014">Read more</a>.
 	</p>
 
         <p>
         <font face="courier" size="3"><b>07 October 2014 -
         Introducing the UCSC Genome Browser Blog</b>: </font>
         We're excited to introduce a new
         <a href="http://genome.ucsc.edu/blog" target="_blank">blog</a> that will feature posts by
         Genome Browser staff and guests.
         <a href="goldenPath/newsarch.html#100714">Read more</a>.
         </p> -->
 
         <!-- start archives -->
         <p>
 	<font face="courier" size="3"><b>30 September 2014 -