Functional-Network-Based Gene Set Analysis Using Gene-Ontology

被引:9
作者
Chang, Billy [1 ,2 ]
Kustra, Rafal [2 ]
Tian, Weidong [1 ]
机构
[1] Fudan Univ, State Key Lab Genet Engn, Inst Biostat, Shanghai 200433, Peoples R China
[2] Univ Toronto, Dalla Lana Sch Publ Hlth, Div Biostat, Toronto, ON, Canada
来源
PLOS ONE | 2013年 / 8卷 / 02期
基金
中国国家自然科学基金;
关键词
P53; EXPRESSION; AMPLIFICATION; BIOLOGY; ARREST; CELLS;
D O I
10.1371/journal.pone.0055635
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To account for the functional non-equivalence among a set of genes within a biological pathway when performing gene set analysis, we introduce GOGANPA, a network-based gene set analysis method, which up-weights genes with functions relevant to the gene set of interest. The genes are weighted according to its degree within a genome-scale functional network constructed using the functional annotations available from the gene ontology database. By benchmarking GOGANPA using a well-studied P53 data set and three breast cancer data sets, we will demonstrate the power and reproducibility of our proposed method over traditional unweighted approaches and a competing network-based approach that involves a complex integrated network. GOGANPA's sole reliance on gene ontology further allows GOGANPA to be widely applicable to the analysis of any gene-ontology-annotated genome.
引用
收藏
页数:13
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