Cargando…
A robust penalized method for the analysis of noisy DNA copy number data
BACKGROUND: Deletions and amplifications of the human genomic DNA copy number are the causes of numerous diseases, such as, various forms of cancer. Therefore, the detection of DNA copy number variations (CNV) is important in understanding the genetic basis of many diseases. Various techniques and p...
| Autores principales: | , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2010
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247090/ https://www.ncbi.nlm.nih.gov/pubmed/20868505 http://dx.doi.org/10.1186/1471-2164-11-517 |