94d4368e9b539a8c369e16a8a950e14799f03cab
jnavarr5
  Tue Aug 11 16:13:45 2026 -0700
Announcing the ClinPred pathogenicity score track for hg19 and hg38, refs #37510

Co-Authored-By: Claude Opus 5 (1M context) <noreply@anthropic.com>

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 <p>You can sign-up to get these announcements via our 
 <a target=_blank href="https://groups.google.com/a/soe.ucsc.edu/g/genome-announce?hl=en">Genome-announce</a>
 email list. We send around one short announcement email every two weeks.</p>
 
 <p>Smaller software changes are not announced here.  A summary of the three-weekly release changes can be 
 found <a target=_blank href="https://genecats.gi.ucsc.edu/builds/versions.html">here</a>. 
 For the full list of our daily code changes head to our <a
 href="https://github.com/ucscGenomeBrowser/kent/commits/master"
 target=_blank>GitHub page</a>. Lastly, see our <a href="credits.html" target="_blank">
 credits page</a> for acknowledgments of the data we host.</p>
 
 <!-- ============= 2026 archived news ============= -->
 
 <a name="2026"></a>
 
+<a name="081126"></a>
+<h2>Aug. 11, 2026 &nbsp;&nbsp; Deleteriousness Predictions: ClinPred for hg19 and hg38</h2>
+<p>
+We are pleased to announce the release of the ClinPred pathogenicity score track for
+<a href="/cgi-bin/hgTrackUi?db=hg19&g=clinPred" target="_blank">hg19</a> and
+<a href="/cgi-bin/hgTrackUi?db=hg38&g=clinPred" target="_blank">hg38</a>.
+ClinPred is a machine-learning predictor of pathogenicity for nonsynonymous (missense)
+single-nucleotide variants, combining existing pathogenicity scores with population allele
+frequency from gnomAD. It was trained on confidently annotated disease-causing and benign
+variants from ClinVar. Pre-computed scores are provided for all possible human missense
+variants in the exome.
+</p>
+
+<p>
+Scores range from 0 to 1, with higher values indicating a greater predicted likelihood
+that a variant is disease-relevant. The authors recommend a score of &ge; 0.5 as evidence
+of pathogenicity. As with any pathogenicity prediction score, ClinPred is intended as
+supporting evidence rather than a stand-alone classifier.
+</p>
+
+<p>
+There are four subtracks in this collection, one for each possible alternate nucleotide
+(A, C, G, T). At every exome position covered by ClinPred, three of the four subtracks
+show a score (one per non-reference base), and the fourth, corresponding to the reference
+base, is set to 0. Synonymous alternates are also set to 0, since ClinPred only scores
+missense variants. Positions with no exome coverage are shown as gaps.
+</p>
+
+<div class="text-center" style="margin-top: 1.5em;">
+<a href="https://genome.ucsc.edu/s/bkitiyakara/share_JMwPz7ty" target="_blank">
+<img alt="Genome Browser screenshot of the ClinPred track" src="/images/newsArchImages/ClinPred.png"
+width='55%'></a>
+<p class="gbsCaption"><em>ClinPred pathogenicity scores for all possible single-nucleotide
+substitutions (A, C, G, and T) at a genomic locus (chr7, GRCh38/hg38). The four ClinPred
+subtracks display predicted pathogenicity scores for each possible alternate allele, where
+higher scores indicate a greater likelihood that the variant is disease-causing.</em></p>
+</div>
+
+<p>
+Items in this track are colored according to score:
+</p>
+
+<ul>
+  <li><span style="color:red;"><b>Red</b></span> &ndash; Likely pathogenic (&ge; 0.5)</li>
+  <li><span style="color:blue;"><b>Blue</b></span> &ndash; Likely benign (&lt; 0.5)</li>
+</ul>
+
+<p>
+<b>Note:</b> Zoom in until every base is visible at the top of the display; otherwise,
+multiple nucleotides will fall under a single pixel, and no score will be shown on the
+mouseover tooltip.
+</p>
+
+<p>
+We would like to thank the ClinPred authors for making the pre-computed scores publicly
+available. This track was developed by Lou Nassar and Max Haeussler with QA by Eliza Alde,
+Jairo Navarro, and Barali Kitiyakara.
+</p>
+
 <a name="072226"></a>
 <h2>Jul. 22, 2026 &nbsp;&nbsp; ENCODE4 cCREs and ENCODE4 Regulation tracks released for human (hg38) and mouse (mm10)</h2>
 <p>
 We are excited to announce our major release of the ENCODE4 data collection on the
 UCSC Genome Browser for both the human (hg38/GRCh38) and mouse (mm10/GRCm38)
 assemblies. This release consists of two major components: the
 <a href="/cgi-bin/hgTrackUi?db=hg38&c=chr7&g=cCREs&position=default" target="_blank">
 <b>ENCODE Registry of cCREs</b></a> (candidate Cis-Regulatory Elements) container,
 and the new
 <a href="/cgi-bin/hgTrackUi?db=hg38&c=chr7&g=wgEncodeReg4&position=default" target="_blank">
 <b>ENCODE4 Regulation</b></a> container, both described in
 <a href="https://www.nature.com/articles/s41586-025-09909-9" target="_blank">
 Moore <em>et al</em>., <em>Nature</em> 2026</a>.
 </p>