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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Detalhes bibliográficos
Main Authors: Colella, Stefano, Yau, Christopher, Taylor, Jennifer M., Mirza, Ghazala, Butler, Helen, Clouston, Penny, Bassett, Anne S., Seller, Anneke, Holmes, Christopher C., Ragoussis, Jiannis
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2007
Assuntos:
Computational Biology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1874617/
https://ncbi.nlm.nih.gov/pubmed/17341461
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkm076
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