Facilitating Collaboration in Rare Genetic Disorders Through Effective Matchmaking in DECIPHER. Issue 10 (20th August 2015) - Chatzimichali, Eleni A.
Abstract DECIPHER helps the clinical community share and compare human genome variants and phenotypes in a database of thousands of anonymous consented patients worldwide. Matchmaking using DECIPHER has resulted in the discovery of many new syndromes and led to over 700 peer‐reviewed publications.