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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...

詳細記述

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書誌詳細
主要な著者: Chen, Gary K., Chang, Xiao, Curtis, Christina, Wang, Kai
フォーマット: Artigo
言語:Inglês
出版事項: Oxford University Press 2013
主題:
オンライン・アクセス: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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