The missing indels: an estimate of indel variation in a human genome and analysis of factors that impede detection.

Saved in:
Bibliographic Details
Title: The missing indels: an estimate of indel variation in a human genome and analysis of factors that impede detection.
Authors: Jiang Y; Centre for Computational Medicine, Hospital for Sick Children, Toronto, ON, M5G 0A4, Canada Center for Biomedical Informatics, School of Computer Science and Technology, Harbin Institute of Technology, Harbin, Heilongjiang, 150001, China., Turinsky AL; Centre for Computational Medicine, Hospital for Sick Children, Toronto, ON, M5G 0A4, Canada., Brudno M; Centre for Computational Medicine, Hospital for Sick Children, Toronto, ON, M5G 0A4, Canada Program in Genetics and Genome Biology, Hospital for Sick Children, Toronto, ON, M5G 0A4, Canada Department of Computer Science, University of Toronto, Toronto, ON, M5S 3G4, Canada brudno@cs.toronto.edu.
Source: Nucleic acids research [Nucleic Acids Res] 2015 Sep 03; Vol. 43 (15), pp. 7217-28. Date of Electronic Publication: 2015 Jun 30.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1362-4962 (Electronic) Linking ISSN: 03051048 NLM ISO Abbreviation: Nucleic Acids Res Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1362-4962
DOI:10.1093/nar/gkv677