79b493d56edd2ffdafebdd20bc69528b3bdfee0a lrnassar Mon Sep 28 15:54:54 2026 -0700 News announcement for the redesigned BLAT search and results pages, with the matching indexNews.html item. The entry carries two anchors: #100726 for the usual date form and #newBLAT, which the blatNewFormNewsUrl hg.conf setting on the BLAT banner points at. The banner announces the switch to the new pages on October 28. refs #37996 diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html index 7c0a1336af5..b4089c6ceac 100644 --- src/hg/htdocs/goldenPath/newsarch.html +++ src/hg/htdocs/goldenPath/newsarch.html @@ -52,30 +52,88 @@
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Smaller software changes are not announced here. A summary of the three-weekly release changes can be found here. For the full list of our daily code changes head to our GitHub page. Lastly, see our credits page for acknowledgments of the data we host.
+ + ++We are happy to announce a redesign of our +BLAT sequence search tool. You can +reach the new pages from the banner on the current BLAT pages now, and they will +become the default on October 28. You will be able to opt out of the new page +and continue to use the classic interface after the change. +
+ ++If you have feedback on the new pages, we would love to hear from you at +our contact page. +We would like to thank Maximilian Haeussler, Lou Nassar, Gerardo Perez, Brian Raney, +and the entire QA team for the design, development, and testing of these features. +
+We are pleased to announce a new track showing the AlphaGenome Variant Impact (AVI) score from Google DeepMind's AlphaGenome Atlas, on the human GRCh38/hg38 assembly. The score combines AlphaGenome's predictions of how a variant affects gene regulation, covering expression, splicing, chromatin accessibility and transcription factor binding across hundreds of cell types, with AlphaMissense predictions for protein-altering changes. The result is a single number that ranks how damaging a substitution is likely to be. Unlike most prediction scores, it covers non-coding variants as well as coding ones, across the whole genome.