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Artikel ; 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  Band 43, Heft 6, Seite(n) 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-Begriff(e) Databases, Genetic ; Exome/genetics ; Genomics ; Humans ; Information Dissemination ; Phenotype
Sprache Englisch
Erscheinungsdatum 2022-03-21
Erscheinungsland United States
Dokumenttyp 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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Zs.A 3586: Hefte anzeigen Standort:
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Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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