Evidence map›Paper›PMID 22443377›Full record

ArticleBMC bioinformatics2012

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

Chia-Ling Huang, John Lamb, Leonid Chindelevitch, Jarek Kostrowicki, Justin Guinney, Charles Delisi, Daniel Ziemek

Abstract read
In one paragraph

Article in BMC bioinformatics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Chia-Ling HuangBioinformatics Graduate Program, and Department of Biomedical Engineering, Boston University, 44 Cummington Street, Boston, MA 02215, USA.
John Lamb
Leonid Chindelevitch
Jarek Kostrowicki
Justin Guinney
Charles Delisi
Daniel Ziemek

Funding

Visant-Predictome: A System for Integration, Mining, Visualization and AnalysisR01GM103502 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI DELISI, CHARLES, HU, ZHENJUN · 2012 to 2015
$3.0M
Visant-Predictome: A System for Integration, Mining, Visualization and AnalysisR01RR022971 · NCRR · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI DELISI, CHARLES, HU, ZHENJUN · 2007 to 2011
$2.1M
NCRR NIH HHS 5R01RR022971-05NIGMS NIH HHS 8 R01 GM103502-05NIGMS NIH HHS R01 GM103502
6 · The paper itself

Abstract

backgroundIdentification 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.

resultsWe 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.

conclusionsCSA 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.

Indexed as

Gene Regulatory NetworksComputational BiologyComputer SimulationFemaleHumansLymphoma, B-CellMetabolic DiseasesOvarian NeoplasmsSample SizeTranscription, Genetic

Identifiers

PMID22443377
PMCPMC3382432

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.