We are pleased to announce the release of the Genomenon Mastermind Variants track for the hg19/GRCh37 assembly. This track is composed of variants found in scientific publications collected by Genomenon Mastermind. Mastermind uses software that searches for disease-gene-variant associations in the scientific literature. The genome browser track shows only if a variant has been indexed by the search engine. Genomenon Mastermind Genomic Search Engine is a commercial database of variants likely to be mentioned in full-text scientific articles.
Genomic locations of variants are labeled with the nucleotide change. Hover over the features to -see the gene, the amino acid change, and the scores MMCNT1, MMCNT2 and MMCNT3, described below. All +see the gene, the amino acid change, and the support scores. All other information is shown on the respective Mastermind variant detail page, accessible via the "Link to Mastermind" at the top of the details page. -More information about this track and it's display can be found on the +More information about this track and its display can be found on the track description page.
We would like to give a big thank you to Mark Kiel, Steve Schwartz and Clayton Wheeler from Genomenon for making this data available as well as Max Haeussler, Conner Powell and the rest of the UCSC Genome Browser team for bringing this track to life.
We are pleased to announce the addition of GRCh38 patches to the GRCh38/hg38 database. Without a release date for the