Core Module Network Construction for Breast Cancer Metastasis

被引:0
|
作者
Yang, Ruoting [1 ]
Daigle, Bernie J., Jr. [2 ]
Petzold, Linda R. [1 ,2 ,3 ]
Doyle, Francis J., III [1 ,4 ]
机构
[1] Univ Calif Santa Barbara, Inst Collaborat Biotechnol, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Comp Sci, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Mech Engn, Santa Barbara, CA 93106 USA
[4] Univ Calif Santa Barbara, Chem Engn, Santa Barbara, CA 93106 USA
关键词
Biomarker; Microarray; Network; Sensitivity; CLASSIFICATION; SIGNATURES; HALLMARKS; RESOURCE;
D O I
暂无
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
For prognostic and diagnostic purposes, it is crucial to be able to separate the group of "driver" genes and their first-degree neighbours, (i.e. "core module") from the general "disease module". To facilitate this task, we developed a novel computational framework COMBINER: COre Module Biomarker Identification with Network ExploRation. We applied COMBINER to three benchmark breast cancer datasets for identifying prognostic biomarkers. We generated a list of "driver genes" by finding the common core modules between two sets of COMBINER markers identified with different module inference protocols. Overlaying the markers on the map of "the hallmarks of cancer" and constructing a weighted regulatory network with sensitivity analysis, we validated 29 driver genes. Our results show the COMBINER framework to be a promising approach for identifying and characterizing core modules and driver genes of many complex diseases.
引用
收藏
页码:5083 / 5089
页数:7
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