First genome-wide CNV mapping in FELIS CATUS using next generation sequencing data-Reference-Cited by-同舟云学术

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First genome-wide CNV mapping in FELIS CATUS using next generation sequencing data

Published:2018-12 Issue:1 Volume:19 Page:
ISSN:1471-2164
Container-title:BMC Genomics
language:en
Short-container-title:BMC Genomics

Author:

Genova F., ,Longeri M.,Lyons L. A.,Bagnato A.,Strillacci M. G.^ORCID

Funder

Winn Feline Foundation and the George Sydney and Phyllis Redman Miller Trust

National Geographic Society Education Foundation

University of Missouri Gilbreath-McLorn Endowment

Cornell Feline Health Center

contributions from the 99 Lives Consortium participants

Associazione Nazionale Felina Italiana

Zoetis

Orivet Genetic Pet Care, Langford Veterinary Services, the World Cat Federation, and public donations

Università degli Studi di Milano

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Biotechnology

Link

http://link.springer.com/content/pdf/10.1186/s12864-018-5297-2.pdf

Reference57 articles.

1. Bridges CB. The bar “gene” a duplication. Science. 1936;83(2148):210–1.

2. Henrichsen CN, Chaignat E, Reymond A. Copy number variants, diseases and gene expression. Hum Mol Genet. 2009;18(R1):R1–8.

3. Levy S, Sutton G, Ng PC, Feuk L, Halpern AL, Walenz BP, et al. The diploid genome sequence of an individual human. PLoS Biol. 2007;5(10):e254.

4. Sebat J, Lakshmi B, Troge J, Alexander J, Young J, Lundin P, et al. Large-scale copy number polymorphism in the human genome. Science. 2004;305(5683):525–8.

5. Iafrate AJ, Feuk L, Rivera MN, Listewnik ML, Donahoe PK, Qi Y, et al. Detection of large-scale variation in the human genome. Nat Genet. 2004;36(9):949–51.

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