New Tool Developed to Identify Genetic Risk Factors

Using genome-wide association study (GWAS) phenotype-to-genes associations, and pathway data from a free, open-source, curated and peer reviewed pathway database Reactome, they connected human traits based on the common patterns of human biological pathways, detecting more pleiotropic effects, and expanding previous studies from a gene-centric approach to that of shared cell-processes.

PHPN supports the integration of genomic and phenotypic data to uncover significant links between traits, attributes, and disease. This offers tremendous potential in identifying risk factors for certain diseases. At the same time, it can reveal important targets for therapeutic intervention. The automatic classification of phenotypes into “phenotype classes,” using the network’s topological modularity and a standard community detection algorithm, showed very promising results. Two traits that were connected in the PHPN but did not share any common associated genes or any clear-cut biological relationship were von Willebrand factor and FVIII levels (vWF) and hippocampal atrophy (HA).

Christian Darabos, PhD, the lead author of the study, said, “The intuitive network representation of the knowledge mined from several large-scale datasets makes the information accessible to anyone. It lies at the crossroads of computational genetics, systems biology, information theory, and network science. As a proof of concept, the PHPN has proven capable of identifying well-documented interactions, and many novel links that remain to be explored in depth. The PHPN is a hypothesis-generating tool, potentially capable of identifying yet uncharacterized common drug targets.” As a next step, the scientists will refine statistical methods, isolate networks for optimal results, and compare previous work on phenotype networks. The study was published on January 25, 2014, in the journal BioDataMining.

Related Links:
Geisel School of Medicine at Dartmouth
Reactome