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Article ; Online: Variant-level matching for diagnosis and discovery: Challenges and opportunities.

Rodrigues, Eliete da S / Griffith, Sean / Martin, Renan / Antonescu, Corina / Posey, Jennifer E / Coban-Akdemir, Zeynep / Jhangiani, Shalini N / Doheny, Kimberly F / Lupski, James R / Valle, David / Bamshad, Michael J / Hamosh, Ada / Sheffer, Assaf / Chong, Jessica X / Einhorn, Yaron / Cupak, Miro / Sobreira, Nara

Human mutation

2022  Volume 43, Issue 6, Page(s) 782–790

Abstract: Here we describe MyGene2, Geno2MP, VariantMatcher, and Franklin; databases that provide variant-level information and phenotypic features to researchers, clinicians, healthcare providers and patients. Following the footsteps of the Matchmaker Exchange ... ...

Abstract Here we describe MyGene2, Geno2MP, VariantMatcher, and Franklin; databases that provide variant-level information and phenotypic features to researchers, clinicians, healthcare providers and patients. Following the footsteps of the Matchmaker Exchange project that connects exome, genome, and phenotype databases at the gene level, these databases have as one goal to facilitate connection to one another using Data Connect, a standard for discovery and search of biomedical data from the Global Alliance for Genomics and Health (GA4GH).
MeSH term(s) Databases, Genetic ; Exome/genetics ; Genomics ; Humans ; Information Dissemination ; Phenotype
Language English
Publishing date 2022-03-21
Publishing country United States
Document type Journal Article ; Research Support, N.I.H., Extramural
ZDB-ID 1126646-6
ISSN 1098-1004 ; 1059-7794
ISSN (online) 1098-1004
ISSN 1059-7794
DOI 10.1002/humu.24359
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