A Hidden Markov Model for Copy Number Variant prediction from whole genome resequencing data

MOTIVATION: Copy Number Variants (CNVs) are important genetic factors for studying human diseases. While high-throughput whole genome re-sequencing provides multiple lines of evidence for detecting CNVs, computational algorithms need to be tailored for different type or size of CNVs under different...

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Detalles Bibliográficos
Autores principales: Shen, Yufeng, Gu, Yiwei, Pe’er, Itsik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3194192/
https://www.ncbi.nlm.nih.gov/pubmed/21989326
http://dx.doi.org/10.1186/1471-2105-12-S6-S4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3194192/
https://www.ncbi.nlm.nih.gov/pubmed/21989326
http://dx.doi.org/10.1186/1471-2105-12-S6-S4

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