Innovative strategies for annotating the "relationSNP" between variants and molecular phenotypes.

Miller, Jason E; Veturi, Yogasudha; Ritchie, Marylyn D

Miller, Jason E; Veturi, Yogasudha; Ritchie, Marylyn D.

Afiliación

Miller JE; Department of Genetics, Institute for Biomedical Informatics, Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Blvd., Philadelphia, PA 19104 USA.
Veturi Y; Department of Genetics, Institute for Biomedical Informatics, Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Blvd., Philadelphia, PA 19104 USA.
Ritchie MD; Department of Genetics, Institute for Biomedical Informatics, Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Blvd., Philadelphia, PA 19104 USA.

BioData Min ; 12: 10, 2019.

Article en En | MEDLINE | ID: mdl-31114635

Palabras clave

Deep-learning; Machine-learning; Mutation; Non-coding; Non-synonymous; Precision medicine; Resource; SNP; Software; Synonymous; Tools; Variant

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: BioData Min Año: 2019 Tipo del documento: Article

Texto completo

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: BioData Min Año: 2019 Tipo del documento: Article