Heterogeneous Network Edge Prediction: A Data Integration Approach to Prioritize Disease-Associated Genes

被引:97
|
作者
Himmelstein, Daniel S. [1 ]
Baranzini, Sergio E. [1 ,2 ,3 ]
机构
[1] Univ Calif San Francisco, Biol & Med Informat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Neurol, San Francisco, CA USA
[3] Univ Calif San Francisco, Inst Human Genet, San Francisco, CA 94143 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
GENOME-WIDE ASSOCIATION; RANDOM-WALK; C-REL; EXPRESSION; ONTOLOGY; REGULARIZATION; CELLS; TOOL; SET; MAP;
D O I
10.1371/journal.pcbi.1004259
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The first decade of Genome Wide Association Studies (GWAS) has uncovered a wealth of disease-associated variants. Two important derivations will be the translation of this information into a multiscale understanding of pathogenic variants and leveraging existing data to increase the power of existing and future studies through prioritization. We explore edge prediction on heterogeneous networks-graphs with multiple node and edge types-for accomplishing both tasks. First we constructed a network with 18 node types-genes, diseases, tissues, pathophysiologies, and 14 MSigDB (molecular signatures database) collections-and 19 edge types from high-throughput publicly-available resources. From this network composed of 40,343 nodes and 1,608,168 edges, we extracted features that describe the topology between specific genes and diseases. Next, we trained a model from GWAS associations and predicted the probability of association between each protein-coding gene and each of 29 well-studied complex diseases. The model, which achieved 132-fold enrichment in precision at 10% recall, outperformed any individual domain, highlighting the benefit of integrative approaches. We identified pleiotropy, transcriptional signatures of perturbations, pathways, and protein interactions as influential mechanisms explaining pathogenesis. Our method successfully predicted the results (with AUROC = 0.79) from a withheld multiple sclerosis (MS) GWAS despite starting with only 13 previously associated genes. Finally, we combined our network predictions with statistical evidence of association to propose four novel MS genes, three of which (JAK2, REL, RUNX3) validated on the masked GWAS. Furthermore, our predictions provide biological support highlighting REL as the causal gene within its gene-rich locus. Users can browse all predictions online (http://het.io). Heterogeneous network edge prediction effectively prioritized genetic associations and provides a powerful new approach for data integration across multiple domains.
引用
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页数:27
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