增强子
生物
计算生物学
全基因组关联研究
基因组
调节顺序
基因调控网络
基因
人类基因组
电池类型
遗传学
转录因子
遗传关联
基因表达调控
疾病
基因组编辑
系统生物学
转录调控
细胞
基因表达
单核苷酸多态性
基因型
医学
病理
作者
Daniel Marbach,David Lamparter,Gerald Quon,M Kellis,Zoltán Kutalik,Sven Bergmann
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2016-03-07
卷期号:13 (4): 366-370
被引量:326
摘要
This resource contains 394 human cell type– and tissue-specific transcriptional networks and finds that disease-associated genetic variants often perturb regulatory modules in tissues specific for that disease. Mapping perturbed molecular circuits that underlie complex diseases remains a great challenge. We developed a comprehensive resource of 394 cell type– and tissue-specific gene regulatory networks for human, each specifying the genome-wide connectivity among transcription factors, enhancers, promoters and genes. Integration with 37 genome-wide association studies (GWASs) showed that disease-associated genetic variants—including variants that do not reach genome-wide significance—often perturb regulatory modules that are highly specific to disease-relevant cell types or tissues. Our resource opens the door to systematic analysis of regulatory programs across hundreds of human cell types and tissues ( http://regulatorycircuits.org ).
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