Deciphering highly similar multigene family transcripts from Iso-Seq data with IsoCon-Reference-Cited by-同舟云学术

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Deciphering highly similar multigene family transcripts from Iso-Seq data with IsoCon

Published:2018-11-02 Issue:1 Volume:9 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Sahlin Kristoffer,Tomaszkiewicz Marta,Makova Kateryna D.,Medvedev Paul

Funder

U.S. Department of Health & Human Services | NIH | National Center for Advancing Translational Sciences

NSF | BIO | Division of Biological Infrastructure

NSF | Directorate for Computer & Information Science and Engineering | Division of Information and Intelligent Systems

NSF | Directorate for Computer & Information Science and Engineering | Division of Computing and Communication Foundations

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/s41467-018-06910-x.pdf

Reference69 articles.

1. Zarrei, M., MacDonald, J. R., Merico, D. & Scherer, S. W. A copy number variation map of the human genome. Nat. Rev. Genet. 16, 172–183 (2015).

2. Carter, N. P. Methods and strategies for analyzing copy number variation using DNA microarrays. Nat. Genet. 39, S16–S21 (2007).

3. Sudmant, P. H. et al. Diversity of human copy number variation and multicopy genes. Science 330, 641–646 (2010).

4. Redon, R. et al. Global variation in copy number in the human genome. Nature 444, 444–454 (2006).

5. Bailey, J. A., Kidd, J. M. & Eichler, E. E. Human copy number polymorphic genes. Cytogenet. Genome Res. 123, 234–243 (2008).

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