iPcc: a novel feature extraction method for accurate disease class discovery and prediction

被引:16
|
作者
Ren, Xianwen [1 ,2 ]
Wang, Yong [3 ,4 ]
Zhang, Xiang-Sun [3 ,4 ]
Jin, Qi [1 ,2 ]
机构
[1] Chinese Acad Med Sci, MOH Key Lab Syst Biol Pathogens, Inst Pathogen Biol, Beijing 100730, Peoples R China
[2] Peking Union Med Coll, Beijing 100730, Peoples R China
[3] Chinese Acad Sci, Acad Math & Syst Sci, Beijing 100190, Peoples R China
[4] Chinese Acad Sci, Natl Ctr Math & Interdisciplinary Sci, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
GENE-EXPRESSION PROFILES; MICROARRAY ANALYSIS; FEATURE-SELECTION; CLASSIFICATION; CANCER; MODEL; ALGORITHM; CLUSTERS; SUBTYPES; RULES;
D O I
10.1093/nar/gkt343
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gene expression profiling has gradually become a routine procedure for disease diagnosis and classification. In the past decade, many computational methods have been proposed, resulting in great improvements on various levels, including feature selection and algorithms for classification and clustering. In this study, we present iPcc, a novel method from the feature extraction perspective to further propel gene expression profiling technologies from bench to bedside. We define 'correlation feature space' for samples based on the gene expression profiles by iterative employment of Pearson's correlation coefficient. Numerical experiments on both simulated and real gene expression data sets demonstrate that iPcc can greatly highlight the latent patterns underlying noisy gene expression data and thus greatly improve the robustness and accuracy of the algorithms currently available for disease diagnosis and classification based on gene expression profiles.
引用
收藏
页数:11
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