Understanding transcriptional regulatory networks using computational models

被引:30
作者
He, Bing [1 ,3 ,4 ]
Tan, Kai [1 ,2 ,3 ,4 ]
机构
[1] Univ Iowa, Interdisciplinary Grad Program Genet, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[3] Childrens Hosp Philadelphia, Div Oncol, Dept Biomed & Hlth Informat, Philadelphia, PA 19104 USA
[4] Childrens Hosp Philadelphia, Dept Biomed & Hlth Informat, Ctr Childhood Canc Res, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
GENOME-WIDE ANALYSIS; GENE-EXPRESSION DATA; BINDING; DNA; RECONSTRUCTION; INTEGRATION; MICROARRAY; INFERENCE; CIRCUITRY; PLURIPOTENCY;
D O I
10.1016/j.gde.2016.02.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Transcriptional regulatory networks (TRNs) encode instructions for animal development and physiological responses. Recent advances in genomic technologies and computational modeling have revolutionized our ability to construct models of TRNs. Here, we survey current computational methods for inferring TRN models using genome-scale data. We discuss their advantages and limitations. We summarize representative TRNs constructed using genome-scale data in both normal and disease development. We discuss lessons learned about the structure/function relationship of TRNs, based on examining various large-scale TRN models. Finally, we outline some open questions regarding TRNs, including how to improve model accuracy by integrating complementary data types, how to infer condition-specific TRNs, and how to compare TRNs across conditions and species in order to understand their structure/function relationship.
引用
收藏
页码:101 / 108
页数:8
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