GeneYenta specifications

Information


Unique identifier OMICS_14130
Name GeneYenta
Interface Web user interface
Restrictions to use None
Programming languages Javascript
Database management system MySQL
Computer skills Basic
Stability Stable
Maintained Yes

Taxon


  • Primates
    • Homo sapiens

Documentation


Maintainer


  • person_outline Wyeth Wasserman <>

Publication for GeneYenta

GeneYenta in publication

PMCID: 4850887
PMID: 27148566
DOI: 10.1101/mcs.a000372

[…] among the groups and projects using the hpo are the u.k. 100,000 genomes project (rare diseases), the canadian care for rare, phenomecentral (https://phenomecentral.org/), the case matching system geneyenta (), the u.s. national institutes of health undiagnosed diseases program and network, and the sanger institute's deciphering developmental disorders (ddd) () and decipher () databases. […]


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GeneYenta institution(s)
Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, University of British Columbia, Vancouver, BC, Canada; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada; Stanford University, Stanford, CA, USA
GeneYenta funding source(s)
British Columbia Children’s Hospital Foundation as 1st Collaborative Area of Innovation; Genome BC (SOF-195); BC Clinical Genomics Network (#00032); the Canadian Institutes of Health Research (#301221); Canadian Institutes of Health Research Studentship Award; Genome BC and Genome Canada (ABC4DE Project).

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