CNVDeep: deep association of copy number variants with neurocognitive disorders-Reference-Cited by-同舟云学术

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CNVDeep: deep association of copy number variants with neurocognitive disorders

Published:2024-08-29 Issue:1 Volume:25 Page:
ISSN:1471-2105
Container-title:BMC Bioinformatics
language:en
Short-container-title:BMC Bioinformatics

Author:

Rahaie Zahra,Rabiee Hamid R.,Alinejad-Rokny Hamid

Funder

IR National Science Foundation

UNSW Scientia Program Fellowship and the Australian Research Council Discovery Early Career Researcher Award

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1186/s12859-024-05874-8.pdf

Reference30 articles.

1. Zarrei M, MacDonald JR, Merico D, Scherer SW. A copy number variation map of the human genome. Nat Rev Genet. 2015;16(3):172–83. https://doi.org/10.1038/nrg3871.

2. Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD, Fiegler H, Shapero MH, Carson AR, Chen W, Cho EK. Global variation in copy number in the human genome. Nature. 2006;444(7118):444–54. https://doi.org/10.1038/nature05329.

3. St CD. Copy number variation and schizophrenia. Schizophr Bull. 2009;35(1):9–12. https://doi.org/10.1093/schbul/sbn147.

4. Forer L, Schönherr S, Weissensteiner H, Haider F, Kluckner T, Gieger C, Wichmann HE, Specht G, Kronenberg F, Kloss-Brandstätter A. CONAN: copy number variation analysis software for genome-wide association studies. BMC Bioinformatics. 2010;11(1):1–9. https://doi.org/10.1186/1471-2105-11-318.

5. Xu Y, Peng B, Fu Y, Amos CI. Genome-wide algorithm for detecting CNV associations with diseases. BMC Bioinformatics. 2011;12(1):1. https://doi.org/10.1186/1471-2105-12-331.

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