+You can sign-up to get these announcements via our Genome-announce email list. We send around one short announcement email every two weeks.
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 pleased to announce the release of the MITOMAP track for the +hg38/GRCh38 +and hg19/GRCh37 human assemblies. +MITOMAP +is a database of human mitochondrial DNA (mtDNA) variation, allowing users to look up human +mitochondrial gene loci, search public mitochondrial sequences, and browse or search for reported +nucleotide variants in both the general population and clinical disease studies. +
++This release includes two tracks within the MITOMAP composite track: +
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++More information on this composite track can be found on the +track description +page. +
++We would like to thank Shiping Zhang and the entire MITOMAP resource for making these annotations +available. We would also like to thank Max Haeussler, Luis Nassar, and Gerardo Perez for their +efforts on this release. +
+ +We are excited to announce the new Splicing Impact Prediction Scores and Databases super track for the hg38/GRCh38 and hg19/GRCh37 human assemblies. This super track includes the AbSplice Scores, SpliceAI, and, for hg38, the new SpliceVarDB track. SpliceVarDB is an online database consolidating over 50,000 variants assayed for their effects on