tmVar 2.0: integrating genomic variant information from literature with dbSNP and ClinVar for precision medicine.

Wei, Chih-Hsuan; Phan, Lon; Feltz, Juliana; Maiti, Rama; Hefferon, Tim; Lu, Zhiyong

Wei, Chih-Hsuan; Phan, Lon; Feltz, Juliana; Maiti, Rama; Hefferon, Tim; Lu, Zhiyong.

Affiliation

Wei CH; National Center for Biotechnology Information (NCBI), National Library of Medicine (NLM), Bethesda, MD 20894, USA.
Phan L; National Center for Biotechnology Information (NCBI), National Library of Medicine (NLM), Bethesda, MD 20894, USA.
Feltz J; National Center for Biotechnology Information (NCBI), National Library of Medicine (NLM), Bethesda, MD 20894, USA.
Maiti R; National Center for Biotechnology Information (NCBI), National Library of Medicine (NLM), Bethesda, MD 20894, USA.
Hefferon T; National Center for Biotechnology Information (NCBI), National Library of Medicine (NLM), Bethesda, MD 20894, USA.
Lu Z; National Center for Biotechnology Information (NCBI), National Library of Medicine (NLM), Bethesda, MD 20894, USA.

Bioinformatics ; 34(1): 80-87, 2018 01 01.

Article in En | MEDLINE | ID: mdl-28968638

Subject(s)

Data Mining/methods; Mutation; Polymorphism, Genetic; Precision Medicine/methods; Software; Data Curation; Databases, Factual; Genetic Predisposition to Disease; Genomics/methods; Humans; Phenotype; PubMed; Publications

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Full text: 1 Database: MEDLINE Main subject: Polymorphism, Genetic / Software / Precision Medicine / Data Mining / Mutation Limits: Humans Language: En Journal: Bioinformatics Journal subject: INFORMATICA MEDICA Year: 2018 Type: Article Affiliation country: United States

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