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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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| Autores principales: | , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2009
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| Materias: | |
| Acceso en línea: | 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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