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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...
Gorde:
| Egile Nagusiak: | , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BioMed Central
2010
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3247090/ https://ncbi.nlm.nih.gov/pubmed/20868505 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-11-517 |
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