Assembling cell context-specific gene sets: a case in cardiomyopathy

An increasing amount of evidence suggests that canonical pathways and standard molecular signature databases are incomplete and inadequate to model the complex behavior of cell physiology and pathology. Yet, many Gene Set Analysis (GSA) studies still rely on these databases to identify disease bioma...

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Bibliographic Details
Main Authors: Liu Mingming, King Vanessa, Lim Wei Keat
Format: Article
Language:English
Published: De Gruyter 2013-03-01
Series:Journal of Integrative Bioinformatics
Online Access:http://www.degruyter.com/view/j/jib.2013.10.issue-1/biecoll-jib-2013-234/biecoll-jib-2013-234.xml?format=INT
Description
Summary:An increasing amount of evidence suggests that canonical pathways and standard molecular signature databases are incomplete and inadequate to model the complex behavior of cell physiology and pathology. Yet, many Gene Set Analysis (GSA) studies still rely on these databases to identify disease biomarkers and molecular mechanisms within a specific cell context. While tremendous effort has been invested in developing GSA tools, there is limited number of studies focusing on de novo assembly of context-specific gene sets as opposed to simply applying GSA using the standard gene set database.
ISSN:1613-4516