Markov Models for Inferring Copy Number Variations from Genotype Data on Illumina Platforms

BACKGROUND/AIMS: Illumina genotyping arrays provide information on DNA copy number. Current methodology for their analysis assumes linkage equilibrium across adjacent markers. This is unrealistic, given the markers high density, and can result in reduced specificity. Another limitation of current me...

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Enregistré dans:
Détails bibliographiques
Auteurs principaux: Wang, Hui, Veldink, Jan H., Blauw, Hylke, van den Berg, Leonard H., Ophoff, Roel A., Sabatti, Chiara
Format: Artigo
Langue:Inglês
Publié: S. Karger AG 2009
Sujets:
Original Paper
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2880724/
https://ncbi.nlm.nih.gov/pubmed/19339782
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000210445
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