ec36719c2512042954514a774bc6cb9719de826c gperez2 Wed Aug 14 09:41:51 2024 -0700 Announcing the new pop-up dialogue box for item details feature, refs #33216 diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html index 0cfea7a..03e0530 100755 --- src/hg/htdocs/goldenPath/newsarch.html +++ src/hg/htdocs/goldenPath/newsarch.html @@ -54,30 +54,59 @@
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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 excited to introduce the new Item Details feature which simplifies the user experience by +displaying track item details in a pop-up dialogue box. This feature allows the information to be +viewed without the need to navigate away from the current page:
++When a track item is clicked in either pack or full mode, the Item Details dialogue box will +appear. This box can be resized by clicking and dragging the button located in its lower-right +corner. For users who prefer viewing item details on a separate page, clicking the new window +button in the upper-right corner will load the information in a new tab. The dialogue box can be +closed by clicking the x button, the button, pressing +the Escape key, or by clicking outside the box.
++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.
+We 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