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Genome-wide identification of significant aberrations in cancer genome

  • Xiguo Yuan
  • , Guoqiang Yu
  • , Xuchu Hou
  • , Ie Ming Shih
  • , Robert Clarke
  • , Junying Zhang
  • , Eric P. Hoffman
  • , Roger R. Wang
  • , Zhen Zhang
  • , Yue Wang*
  • *此作品的通信作者
  • Xidian University
  • Virginia Polytechnic Institute and State University
  • Stanford University
  • Johns Hopkins University
  • Georgetown University
  • Children's National Medical Center
  • Richard Montgomery High School

研究成果: 期刊稿件文章同行評審

33 引文 斯高帕斯(Scopus)

摘要

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 Aberration in Cancer (SAIC), a new method for characterizing and assessing the statistical significance of recurrent CNA units. Three main features of SAIC include: (1) exploiting the intrinsic correlation among consecutive probes to assign a score to each CNA unit instead of single probes; (2) performing permutations on CNA units that preserve correlations inherent in the copy number data; and (3) iteratively detecting Significant Copy Number Aberrations (SCAs) and estimating an unbiased null distribution by applying an SCA-exclusive permutation scheme.Results: We test and compare the performance of SAIC against four peer methods (GISTIC, STAC, KC-SMART, CMDS) on a large number of simulation datasets. Experimental results show that SAIC outperforms peer methods in terms of larger area under the Receiver Operating Characteristics curve and increased detection power. We then apply SAIC to analyze structural genomic aberrations acquired in four real cancer genome-wide copy number data sets (ovarian cancer, metastatic prostate cancer, lung adenocarcinoma, glioblastoma). When compared with previously reported results, SAIC successfully identifies most SCAs known to be of biological significance and associated with oncogenes (e.g., KRAS, CCNE1, and MYC) or tumor suppressor genes (e.g., CDKN2A/B). Furthermore, SAIC identifies a number of novel SCAs in these copy number data that encompass tumor related genes and may warrant further studies.Conclusions: Supported by a well-grounded theoretical framework, SAIC has been developed and used to identify SCAs in various cancer copy number data sets, providing useful information to study the landscape of cancer genomes. Open-source and platform-independent SAIC software is implemented using C++, together with R scripts for data formatting and Perl scripts for user interfacing, and it is easy to install and efficient to use. The source code and documentation are freely available at http://www.cbil.ece.vt.edu/software.htm.

原文英語
文章編號342
期刊BMC Genomics
13
發行號1
DOIs
出版狀態已出版 - 27 07 2012
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UN SDG

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  1. SDG3 健康與福祉
    SDG3 健康與福祉

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