Correlation set analysis: detecting active regulators in disease populations using prior causal knowledge.

Correlation set analysis: detecting active regulators in disease populations using prior causal knowledge.
复制标题

DOI:
10.1186/1471-2105-13-46
复制
发表时间:
2012-03-23
期刊:
影响因子:
3
通讯作者:
Ziemek D
Ziemek D
中科院分区:
生物学4区
文献类型:
--
作者:
Huang CL;Lamb J;Chindelevitch L;Kostrowicki J;Guinney J;Delisi C;Ziemek D

文献摘要

参考文献

被引文献

相似文献

Identification of active causal regulators is a crucial problem in understanding mechanism of diseases or finding drug targets. Methods that infer causal regulators directly from primary data have been proposed and successfully validated in some cases. These methods necessarily require very large sample sizes or a mix of different data types. Recent studies have shown that prior biological knowledge can successfully boost a method's ability to find regulators. We present a simple data-driven method, Correlation Set Analysis (CSA), for comprehensively detecting active regulators in disease populations by integrating co-expression analysis and a specific type of literature-derived causal relationships. Instead of investigating the co-expression level between regulators and their regulatees, we focus on coherence of regulatees of a regulator. Using simulated datasets we show that our method performs very well at recovering even weak regulatory relationships with a low false discovery rate. Using three separate real biological datasets we were able to recover well known and as yet undescribed, active regulators for each disease population. The results are represented as a rank-ordered list of regulators, and reveals both single and higher-order regulatory relationships. CSA is an intuitive data-driven way of selecting directed perturbation experiments that are relevant to a disease population of interest and represent a starting point for further investigation. Our findings demonstrate that combining co-expression analysis on regulatee sets with a literature-derived network can successfully identify causal regulators and help develop possible hypothesis to explain disease progression.
DOI: 10.1186/gb-2010-11-2-r23
发表时间: 2010
期刊: Genome biology
影响因子: 12.3
作者:
Hung JH;Whitfield TW;Yang TH;Hu Z;Weng Z;DeLisi C
通讯作者: DeLisi C
3T3-L1 细胞早期脂肪形成的转录组分析和启动子序列研究。
DOI: 10.4162/nrp.2007.1.1.19
发表时间: 2007
影响因子: 2.4
作者:
Kim, Su-Jong;Lee, Ki-Hwan;Lee, Yong-Sung;Mun, Eun-Gyeng;Kwon, Dae-Young;Cha, Youn-Soo
通讯作者: Cha, Youn-Soo
DOI: 10.1152/ajpendo.90511.2008
发表时间: 2009-06
期刊: American journal of physiology. Endocrinology and metabolism
影响因子: --
作者:
Madani R;Karastergiou K;Ogston NC;Miheisi N;Bhome R;Haloob N;Tan GD;Karpe F;Malone-Lee J;Hashemi M;Jahangiri M;Mohamed-Ali V
通讯作者: Mohamed-Ali V
以TF为中心的下游基因集富集分析:通过整合TF-DNA相互作用和蛋白质翻译后修饰信息来推断因果调节因子
DOI: 10.1186/1471-2105-11-s11-s5
发表时间: 2010-12-14
期刊: BMC bioinformatics
影响因子: 3
作者:
Liu Q;Tan Y;Huang T;Ding G;Tu Z;Liu L;Li Y;Dai H;Xie L
通讯作者: Xie L
DOI: 10.1074/jbc.m109.093955
发表时间: 2010-03-19
影响因子: 4.8
作者:
Pi, Jingbo;Leung, Laura;Chan, Jefferson Y.
通讯作者: Chan, Jefferson Y.