Abstract

Tissue and cell-type identity lie at the core of human physiology and disease. Understanding the genetic underpinnings of complex tissues and individual cell lineages is crucial for developing improved diagnostics and therapeutics. We present genome-wide functional interaction networks for 144 human tissues and cell types developed using a data-driven Bayesian methodology that integrates thousands of diverse experiments spanning tissue and disease states. Tissue-specific networks predict lineage-specific responses to perturbation, identify the changing functional roles of genes across tissues and illuminate relationships among diseases. We introduce NetWAS, which combines genes with nominally significant genome-wide association study (GWAS) P values and tissue-specific networks to identify disease-gene associations more accurately than GWAS alone. Our webserver, GIANT, provides an interface to human tissue networks through multi-gene queries, network visualization, analysis tools including NetWAS and downloadable networks. GIANT enables systematic exploration of the landscape of interacting genes that shape specialized cellular functions across more than a hundred human tissues and cell types.

Keywords

BiologyGenome-wide association studyMulticellular organismComputational biologyCell typeGene regulatory networkGenomeGeneFunction (biology)DiseaseHuman genomeGeneticsCellGene expression

MeSH Terms

Alzheimer DiseaseBayes TheoremCellsCulturedGene Expression RegulationGene OntologyGene Regulatory NetworksGenome-Wide Association StudyHumansHypertensionModelsBiologicalMyocytesSmooth MuscleOrgan SpecificityParkinson DiseaseProtein Interaction Maps

Affiliated Institutions

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Publication Info

Year
2015
Type
article
Volume
47
Issue
6
Pages
569-576
Citations
889
Access
Closed

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Social media, news, blog, policy document mentions

Citation Metrics

889
OpenAlex
59
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Cite This

Casey S. Greene, Arjun Krishnan, Aaron K. Wong et al. (2015). Understanding multicellular function and disease with human tissue-specific networks. Nature Genetics , 47 (6) , 569-576. https://doi.org/10.1038/ng.3259

Identifiers

DOI
10.1038/ng.3259
PMID
25915600
PMCID
PMC4828725

Data Quality

Data completeness: 86%