SNPnexus: assessing the functional relevance of genetic variation to facilitate the promise of precision medicine-Reference-Cited by-同舟云学术

SNPnexus: assessing the functional relevance of genetic variation to facilitate the promise of precision medicine

Published:2018-05-11 Issue:W1 Volume:46 Page:W109-W113
ISSN:0305-1048
Container-title:Nucleic Acids Research
language:en
Short-container-title:

Author:

Dayem Ullah Abu Z¹,Oscanoa Jorge¹,Wang Jun²^ORCID,Nagano Ai²,Lemoine Nicholas R²,Chelala Claude¹³

Affiliation:

1. Bioinformatics Unit, Centre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London, London EC1M 6BQ, UK

2. Centre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London, London EC1M 6BQ, UK

3. Centre for Computational Biology, Life Sciences Initiative, Queen Mary University of London, London EC1M 6BQ, UK

Funder

London Charity Strategic Research Large Project

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/46/W1/W109/25110473/gky399.pdf

Reference30 articles.

1. SNPnexus: a web server for functional annotation of novel and publicly known genetic variants (2012 update);Dayem Ullah;Nucleic Acids Res.,2012

2. SNPnexus: a web database for functional annotation of newly discovered and public domain Single Nucleotide Polymorphisms;Chelala;Bioinformatics,2009

3. A practical guide for the functional annotation of genetic variations using SNPnexus;Dayem Ullah;Brief Bioinform.,2013

4. Tabix: fast retrieval of sequence features from generic TAB-delimited files;Li;Bioinformatics,2011

5. dbSNP: the NCBI database of genetic variation;Sherry;Nucleic Acids Res.,2001

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