Innovative strategies for annotating the “relationSNP” between variants and molecular phenotypes-Reference-Cited by-同舟云学术

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Innovative strategies for annotating the “relationSNP” between variants and molecular phenotypes

Published:2019-05-14 Issue:1 Volume:12 Page:
ISSN:1756-0381
Container-title:BioData Mining
language:en
Short-container-title:BioData Mining

Author:

Miller Jason E.,Veturi Yogasudha,Ritchie Marylyn D.^ORCID

Funder

National Human Genome Research Institute

National Institute of General Medical Sciences

Publisher

Springer Science and Business Media LLC

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Genetics,Molecular Biology,Biochemistry

Link

http://link.springer.com/content/pdf/10.1186/s13040-019-0197-9.pdf

Reference171 articles.

1. Venter JC, Adams MD, Myers EW, Li PW, Mural RJ, Sutton GG, et al. The sequence of the human genome. Science. American Association for the Advancement of Science. 2001;291:1304–51.

2. Collins FS, Morgan M, Patrinos A. The human genome project: lessons from large-scale biology. Science. 2003;300:286.

3. Collins FS, Patrinos A, Jordan E, Chakravarti A, Gesteland R, Walters L, et al. New Goals for the U.S. Human Genome Project: 1998–2003. Science. American Association for the Advancement of Science. 1998;282:682–9.

4. Gabriel C, Fürst D, Faé I, Wenda S, Zollikofer C, Mytilineos J, et al. HLA typing by next-generation sequencing - getting closer to reality. Tissue Antigens. Wiley/Blackwell. 2014;83(10.1111):65–75.

5. Narzisi G, Schatz MC. The challenge of small-scale repeats for indel discovery. Front Bioeng Biotechnol. 2015;3:8.

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