Variational Inference for Coupled Hidden Markov Models Applied to the Joint Detection of Copy Number Variations
Author:
Affiliation:
1. School of Mathematics and Statistics , Shandong University (Weihai) , Weihai, Shandong , China
2. UMR MIA-Paris, AgroParisTech, INRA , Université Paris-Saclay , Paris , France
Abstract
Publisher
Walter de Gruyter GmbH
Subject
Statistics, Probability and Uncertainty,General Medicine,Statistics and Probability
Link
https://www.degruyter.com/document/doi/10.1515/ijb-2018-0023/pdf
Reference53 articles.
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2. Lucito R, Healy J, Alexander J, Reiner A, Esposito D, Chi M, et al. Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation. Genome Res. 2003;13:2291–305.
3. 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;305:525–8.
4. MacDonald JR, Ziman R, Yuen RKC, Feuk L, Scherer SW. The database of genomic variants: a curated collection of structural variation in the human genome. Nucleic Acids Res. 2014;42:D986–92.
5. Carvalho CM, Lupski JR. Mechanisms underlying structural variant formation in genomic disorders. Nat Rev Genet. 2016;17:224–38.
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