A research roadmap for next-generation sequencing informatics-Reference-Cited by-同舟云学术

A research roadmap for next-generation sequencing informatics

Published:2016-04-20 Issue:335 Volume:8 Page:
ISSN:1946-6234
Container-title:Science Translational Medicine
language:en
Short-container-title:Sci. Transl. Med.

Author:

Altman Russ B.¹,Prabhu Snehit²,Sidow Arend³,Zook Justin M.⁴⁵,Goldfeder Rachel⁶,Litwack David⁷,Ashley Euan⁸,Asimenos George⁹,Bustamante Carlos D.²,Donigan Katherine⁷,Giacomini Kathleen M.¹⁰,Johansen Elaine⁷,Khuri Natalia¹¹,Lee Eunice⁷,Liang Xueying Sharon⁷,Salit Marc⁴¹¹⁵,Serang Omar⁹,Tezak Zivana⁷,Wall Dennis P.¹²,Mansfield Elizabeth⁷,Kass-Hout Taha⁷

Affiliation:

1. Bioengineering, Genetics, and Medicine, Stanford University, Stanford, CA 94305, USA.

2. Biomedical Data Science and Genetics, Stanford University, Stanford, CA 94305, USA.

3. Pathology and Genetics, Stanford University, Stanford, CA 94305, USA.

4. Material Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, USA.

5. Material Measurement Laboratory, National Institute of Standards and Technology, Stanford University, Stanford, CA 94305, USA.

6. Biomedical Informatics, Stanford University, Stanford, CA 94305, USA.

7. Food and Drug Administration, Silver Spring, MD 20993, USA.

8. Medicine, Genetics, and Pathology, Stanford University, Stanford, CA 94305, USA.

9. DNAnexus, Mountain View, CA 94040, USA.

10. Bioengineering and Therapeutic Sciences, University of California at San Francisco, San Francisco, CA 94143, USA.

11. Bioengineering, Stanford University, Stanford, CA 94305, USA.

12. Systems Medicine and Psychiatry, Stanford University, Stanford, CA 94305, USA.

Abstract

Progress in nine research areas will help generate the knowledge required to advance next-generation sequencing diagnostics to the clinic.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

Reference3 articles.

1. PMI https://www.whitehouse.gov/precision-medicine.

2. Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls

3. ART: a next-generation sequencing read simulator

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