fe12d67496ceaf04165c6a5174241906f25a08d5 jnavarr5 Mon Aug 19 16:18:57 2024 -0700 Fixing a typo found via code review, refs #34313 diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html index 03e0530..54f9e3a 100755 --- src/hg/htdocs/goldenPath/newsarch.html +++ src/hg/htdocs/goldenPath/newsarch.html @@ -86,31 +86,31 @@

If desired, this feature can be disabled by unchecking the "Enable pop-up when clicking items option" on the Configure page. You can access the Configure page by selecting Configure under Genome Browser in the blue bar menu, by clicking the button below the browser graphic, or by using the keyboard shortcut "c f".

We would like to thank Christopher Lee, Lou Nassar, Jairo Navarro, and Gerardo Perez for their work on this release.

Aug. 12, 2024    Illumina SpliceAI tracks for human (hg38 and hg19)

-We pleased to announce the release of the Illumina SpliceAI tracks for the +We are pleased to announce the release of the Illumina SpliceAI tracks for the hg38 and hg19 human assemblies. SpliceAI is an open-source deep learning splicing prediction algorithm that can predict splicing alterations caused by DNA variations. Such variants may activate nearby cryptic splice sites, leading to abnormal transcript isoforms. SpliceAI was developed at Illumina; a lookup tool is provided by the Broad institute.

Important: The SpliceAI data on the UCSC Genome Browser is directly from Illumina. However, since SpliceAI refers to the algorithm, and not the computed dataset, the data on the Broad server or other sources may have some differences between them. The SpliceAI scores are made available by Illumina only for academic or not-for-profit research only. By accessing the SpliceAI data, you acknowledge and agree that you may only use this data for your own personal academic or not-for-profit research only, and not for any other purposes.