754e533ae2a773365fbd26d1db114d079659a001 dschmelt Thu Nov 18 14:26:09 2021 -0800 Last edits before announcing orphadata refs #14319 diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html index faccc83..7029dec 100755 --- src/hg/htdocs/goldenPath/newsarch.html +++ src/hg/htdocs/goldenPath/newsarch.html @@ -47,32 +47,32 @@ </ul> </div> </div> </div> <!-- ============= 2021 archived news ============= --> <a name="111821"></a> <h2>Nov. 18, 2021 New Clinical Rare Disease track - Orphadata</h2> <p> We are happy to share another clinical resource for genetic disease correlation, <a href="/cgi-bin/hgTrackUi?db=hg38&g=orphadata">the Orphadata track</a> from <a target="_blank" href="https://www.orpha.net/">the Orphanet consortium</a>. This track shows nearly 8000 genes, on hg19 and hg38, annotated with human disorders and epidemiological information including Human Phenotype Ontology (HPO) disorder name, association type, -modes of inheritance, age of first symptoms, and disease prevalence. This data -is gathered by a consortium of more than 40 countries, focusing +modes of inheritance, age of first symptoms, and disease prevalence (if available). +This data is gathered by a consortium of more than 40 countries, focusing on rare diseases. This track includes gene-disease display filters based on association type, inheritance mode, and age of symptom onset. </p> <p> Orphadata can be found on the Browser in the Phenotype and Literature track group, natively interfacing with other UCSC Genome Browser tools such as the JSON API, Table Browser, and Data Integrator. We would like to thank the Orphanet team for providing this data. We would also like to thank the UCSC affiliates Chris Lee, Tiana Pereira, and Daniel Schmelter for the creation and release of these tracks. </p> <a name="111721"></a> <h2>Nov. 17, 2021 Releasing A New Genome Browser Track Group: Single-Cell RNA-seq</h2> <p>