bdd3f5a412a44554713624dbf478a7288653287f
mspeir
  Tue Mar 8 15:24:43 2016 -0800
Adding missing word to announcement. no redmine.

diff --git src/hg/htdocs/indexNews.html src/hg/htdocs/indexNews.html
index daefda1..733c8b4 100755
--- src/hg/htdocs/indexNews.html
+++ src/hg/htdocs/indexNews.html
@@ -28,31 +28,31 @@
           <P>
           To receive announcements of new genome 
           assembly releases, new software features, updates and 
           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>
   <font color="#006666" size="4"><b>8 Mar 2016
   - Combine Multiple Regions of the Genome Browser into a Single Visualization!</b></font>
   <p>
-  Have ever wished you could remove all of the intronic or intergenic regions from the
+  Have you ever wished you could remove all of the intronic or intergenic regions from the
   Genome Browser display? Have you ever dreamed of being able to visualize multiple
   far-flung regions of a genome? Well, now you can with the new &quot;multi-region&quot; option
   in the Genome Browser!
   </p>
 
   <p>
   The multi-region modes provide four different ways to manipulate the display.
   First, we have an &quot;exon-only&quot; mode that allows you to
   remove all of the intergenic and intronic sequences from the display, leaving you with
   only the exonic regions. Next, there is the &quot;gene-only&quot; mode allowing you to remove only
   the intergenic regions from the display, leaving the genes with exons and introns intact.
   Then there is the &quot;custom regions&quot; mode that allows you to use a remote BED file to
   specify the regions you are interested in viewing alongside each other. Lastly, for human
   assemblies hg17 and newer, there is the &quot;alternative haplotype&quot; mode that allows you to
   view a haplotype sequence inserted into its position in the reference genome.