A Bayesian Analysis for Identifying DNA Copy Number Variations Using a Compound Poisson Process

To study chromosomal aberrations that may lead to cancer formation or genetic diseases, the array-based Comparative Genomic Hybridization (aCGH) technique is often used for detecting DNA copy number variants (CNVs). Various methods have been developed for gaining CNVs information based on aCGH data....

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Detalles Bibliográficos
Autores principales: Chen, Jie, Yiğiter, Ayten, Wang, Yu-Ping, Deng, Hong-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171362/
https://www.ncbi.nlm.nih.gov/pubmed/20976296
http://dx.doi.org/10.1155/2010/268513

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171362/
https://www.ncbi.nlm.nih.gov/pubmed/20976296
http://dx.doi.org/10.1155/2010/268513

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