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A Statistical Change Point Model Approach for the Detection of DNA Copy Number Variations in Array CGH Data

Array comparative genomic hybridization (aCGH) provides a high-resolution and high-throughput technique for screening of copy number variations (CNVs) within the entire genome. This technique, compared to the conventional CGH, significantly improves the identification of chromosomal abnormalities. H...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Chen, Jie, Wang, Yu-Ping
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2009
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4154476/
https://ncbi.nlm.nih.gov/pubmed/19875853
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1109/TCBB.2008.129
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