2125538ce566450c32acefe3771d93c4857d1b2b
gperez2
  Thu Sep 1 11:53:30 2022 -0700
Updating news for Illumina Array tracks, refs #29309 #29492

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     <div class="col-sm-3">
       <ul>
         <li><a href="#2006">2006 News</a></li>
         <li><a href="#2005">2005 News</a></li>
         <li><a href="#2004">2004 News</a></li>
         <li><a href="#2003">2003 News</a></li>
         <li><a href="#2001">2001</a>-<a href="#2002">2002 News</a></li>
       </ul>
     </div>
   </div> 
 </div>
 
 <!-- ============= 2022 archived news ============= -->
 <a name="2022"></a>
 
+<a name="083122"></a>
+<h2>Aug. 31, 2022 &nbsp;&nbsp; New Illumina Array tracks for hg19 and hg38</h2>
+<p>
+We are pleased to announce the addition of new
+<a href="https://www.illumina.com/" target="_blank">Illumina</a> Array tracks for the
+<a href="../cgi-bin/hgTrackUi?db=hg38&g=genotypeArrays" target="_blank">GRCh38/hg38</a> and
+<a href="../cgi-bin/hgTrackUi?db=hg19&g=genotypeArrays" target="_blank">GRCh37/hg19</a>  human
+assemblies. These tracks are contained in the Array Probsets composite track.
+<ul>
+  <li><b>Illumina 450k</b> - Illumina 450k Methylation Array</li>
+  <li><b>Illumina 850k</b> - Illumina 850k EPIC Methylation Array</li>
+  <li><b>CytoSNP 850k</b> - Illumina 850k CytoSNP Array</li>
+</ul></p>
+<p>
+The Illumina 450k and 850k tracks quantitatively interrogate methylation sites across the genome at
+single-nucleotide resolution. The Illumina 850k CytoSNP track contains approximately 850,000
+empirically selected SNPs spanning the entire genome with enriched coverage for 3,262 genes of known
+cytogenetics relevance in both constitutional and cancer applications.</p>
+<p>
+We would like to thank Illumina for providing the data. We would also like to thank Jairo Navarro,
+Brooke Rhead, and Gerardo Perez for their efforts on this release.</p>
+
 <a name="082222"></a>
 <h2>Aug. 22, 2022 &nbsp;&nbsp; dbSNP build 155 tracks for hg19 and hg38</h2>
 <p>
 We are pleased to announce the release of
 <a href="https://www.ncbi.nlm.nih.gov/SNP/" target="_blank">NCBI's dbSNP</a> build 155 data for
 <a href="../cgi-bin/hgTrackUi?db=hg38&g=dbSnp155Composite" target="_blank">GRCh38/hg38</a> and
 <a href="../cgi-bin/hgTrackUi?db=hg19&g=dbSnp155Composite" target="_blank">GRCh37/hg19</a>  human
 assemblies. The release reaches a new milestone of over 1 billion RefSNP (rs) records. For hg38
 (GRCh38), approximately 998 million distinct variants (RefSNP clusters with rs# ids) have been
 mapped to more than 1.06 billion genomic locations including alternate haplotype and fix patch
 sequences. dbSNP remapped variants from hg38 to hg19 (GRCh37); approximately 981 million distinct
 variants were mapped to more than 1.02 billion genomic locations including alternate haplotype and
 fix patch sequences (not all of which are included in UCSC's hg19).</p>
 
 <p>