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

Author:

Wei Chih-Hsuan1ORCID,Phan Lon1,Feltz Juliana1,Maiti Rama1,Hefferon Tim1,Lu Zhiyong1

Affiliation:

1. National Center for Biotechnology Information (NCBI), National Library of Medicine (NLM), Bethesda, MD, USA

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Reference34 articles.

1. OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders, Nuclear.;Amberger;Acids Res,2015

2. OSIRIS: a tool for retrieving literature about sequence variants;Bonis;Bioinformatics,2006

3. Hybrid curation of gene-mutation relations combining automated extraction and crowdsourcing;Burger;Database J. Biol. Datab. Cur,2014

4. MutationFinder: a high-performance system for extracting point mutation mentions from text;Caporaso;Bioinformatics,2007

5. Database resources of the National Center for Biotechnology Information;Coordinators;Nucleic Acids Res,2016

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