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Precise inference of copy number alterations in tumor samples from SNP arrays
Motivation: The accurate detection of copy number alterations (CNAs) in human genomes is important for understanding susceptibility to cancer and mechanisms of tumor progression. CNA detection in tumors from single nucleotide polymorphism (SNP) genotyping arrays is a challenging problem due to pheno...
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2013
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3834792/ https://ncbi.nlm.nih.gov/pubmed/24021380 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btt521 |
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