QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

Array-based technologies have been used to detect chromosomal copy number changes (aneuploidies) in the human genome. Recent studies identified numerous copy number variants (CNV) and some are common polymorphisms that may contribute to disease susceptibility. We developed, and experimentally valida...

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Detalles Bibliográficos
Autores principales: Colella, Stefano, Yau, Christopher, Taylor, Jennifer M., Mirza, Ghazala, Butler, Helen, Clouston, Penny, Bassett, Anne S., Seller, Anneke, Holmes, Christopher C., Ragoussis, Jiannis
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
Materias:
Computational Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1874617/
https://www.ncbi.nlm.nih.gov/pubmed/17341461
http://dx.doi.org/10.1093/nar/gkm076

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1874617/
https://www.ncbi.nlm.nih.gov/pubmed/17341461
http://dx.doi.org/10.1093/nar/gkm076

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