3b3ce5f1e11f04b4a4919f8aa05bac11c8310067 gperez2 Tue May 16 16:36:12 2023 -0700 Fixing grammar errors for the DGV Gold Standard track announcement found by b0b, refs #30908 diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html index 7e59ddb..6f5a6bc 100755 --- src/hg/htdocs/goldenPath/newsarch.html +++ src/hg/htdocs/goldenPath/newsarch.html @@ -181,31 +181,31 @@ assigned to variants that have not been characterized yet. </ul> <p> We would like to thank the <a href="https://www.ebi.ac.uk/eva/" target="_blank">European Variation Archive</a> making this data publically available. We would also like to thank Luis Nassar and Jairo Navarro for the creation and release of these tracks. </p> <a name="042423"></a> <h2>Apr. 24, 2023 New DGV Gold Standard track for hg38</h2> <p> We are pleased to announce the addition of the new <a href="/cgi-bin/hgTrackUi?db=hg38&g=dgvPlus" target="_blank">DGV Gold Standard track</a> for hg38. The track displays curated variants from a selected number of studies in the <a href="http://dgv.tcag.ca/dgv/app/home" target="_blank">Database of Genomic Variants</a> (DGV) -with a criteria that require a variant to be found in at least two different studies and found in +with a criterion that requires a variant to be found in at least two different studies and found in at least two different samples. More information on this track can be found on the <a href="/cgi-bin/hgTrackUi?db=hg38&g=dgvPlus#TRACK_HTML" target="_blank">track description page</a>.</p> <p> We would like to thank the Database of Genomic Variants for making these data available. We would also like to thank Lou Nassar, Anna Benet-Pages, and Gerardo Perez for their efforts on this release.</p> <a name="041423"></a> <h2>Apr. 14, 2023 Problematic Regions for hg38 and a new public hub</h2> <p> We would like to announce the release of the <a target="_blank" href="/cgi-bin/hgTrackUi?db=hg38&position=default&g=problematic">Problematic Regions</a> composite track to show problematic/special genomic regions for sequencing or very variable regions for GRCh38/hg38. This container track helps call out sections of the genome that often cause problems or