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Genome-wide identification of significant aberrations in cancer genome
BACKGROUND: Somatic Copy Number Alterations (CNAs) in human genomes are present in almost all human cancers. Systematic efforts to characterize such structural variants must effectively distinguish significant consensus events from random background aberrations. Here we introduce Significant Aberrat...
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| Главные авторы: | , , , , , , , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BioMed Central
2012
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3428679/ https://ncbi.nlm.nih.gov/pubmed/22839576 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-13-342 |
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