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We are happy to announce the release of the new COSMIC track for hg19/GRCh37 and an update for the hg38/GRCh38 COSMIC track. More information is available at genome.ucsc.edu/goldenPath/new….

The Clinical Interpretation of Variants in Cancer (CIViC) track for hg19/GRCh37 and hg38/GRCh38 is now available. The details page for a feature will list diseases and therapies that have been associated with a genomic variant. Learn more at: genome.ucsc.edu/goldenPath/new…

We are happy to announce the release of new highlight features for track hubs. Items can now be striped with a colored background to appear "highlighted" compared to the other items in the display. Learn more about this release at: genome.ucsc.edu/goldenPath/new…

We are pleased to announce the release of the MITOMAP track for hg38/hg19. MITOMAP is a human mitochondrial genome database. This release includes the MITOMAP Control and Coding Variants track & the MITOMAP Disease Mutations track. Learn more at genome.ucsc.edu/goldenPath/new….

We are excited to share AlphaMissense tracks for the hg38/hg19 human assemblies. AlphaMissense scores, generated by Google DeepMind, predict the pathogenicity of missense variants for all possible single AA substitutions in the human proteome. Learn more: genome.ucsc.edu/goldenPath/new…

We are excited to announce the release of two denovo-db tracks for hg19/GRCh37. denovo-db is a curated database of germline de novo variants in the human genome, defined as variants present in children but absent in their parents. Learn more at: genome.ucsc.edu/goldenPath/new…

A new hub has been added to the Public Hubs listing, EPIration - an atlas of candidate enhancer-gene interactions in human tissues and cell lines. View this hub using the following URL: genome.ucsc.edu/cgi-bin/hgHubC… We want to thank the Guigó Lab for making this data available.

Announcing the new Pseudogenes track for hg38! The composite track contains pseudogene predictions and their corresponding parent genes, as identified by PseudoPipe. This release includes the Pseudogene Parents and Pseudogenes tracks. Learn more at genome.ucsc.edu/goldenPath/new….

We are happy to announce an update to the VISTA Enhancers tracks for hg38, hg19, mm39, and mm10. Learn more about the release from the following news post: genome.ucsc.edu/goldenPath/new…

New tracks now available: GENCODE "knownGene" V48 for human (hg38/hg19) and VM37 for mouse (mm39). Read more about this release in this news post: genome.ucsc.edu/goldenPath/new…

We are excited to announce the release of the Varaico tracks for human assemblies hg38 and hg19. Varaico stands for "Variation Research Advancing Insight in Complex Organisms". Varaico was created using literature mining, similar to AVADA. Learn more at: genome.ucsc.edu/goldenPath/new…

Are you at #eshg2025? Visit us at booth 226! We will also be co-presenting a workshop on Monday, 5/26, with Ensembl at 14:15.

We are happy to announce the release of the EVA SNP Release 7 tracks, now available for 40 assemblies and covering nearly 910 million variants. Learn more at genome.ucsc.edu/goldenPath/new….