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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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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2013
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| Assuntos: | |
| Acesso em linha: | 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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