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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...

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Bibliografski detalji
Glavni autori: Chen, Jie, Wang, Yu-Ping
Format: Artigo
Jezik:Inglês
Izdano: 2009
Teme:
Online pristup: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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