DIagram connecting MME partners

The Matchmaker Exchange: A Platform for Rare Disease Discovery.

There are few better examples of the need for data sharing than in the rare disease community, where patients, physicians, and researchers must search for “the needle in a haystack” to uncover rare, novel causes of disease within the genome. Impeding the pace of discovery …

A rainbow graphic.

UCSC Receives $1M Simons Foundation Grant to Create Human Genetic Variation Map

NEW YORK (GenomeWeb) – Researchers at the University of California Santa Cruz’s Genomics Institute have received a grant for up to $1 million from the Simons Foundation that will support a one-year pilot project to create a comprehensive map of human genetic variation for biomedical …