An Effector Index to Predict Causal Genes at GWAS Loci

Forgetta, V.; Jiang, L.; Vulpescu, N. A.; Hogan, M. S.; Chen, S.; Morris, J. A.; Grinek, S.; Benner, C.; Mccarthy, M. I.; Fauman, E.; Greenwood, C. M.; Maurano, M. T.; Richards, J. B.

doi:10.1101/2020.06.28.171561

bioRxiv · 10.1101/2020.06.28.171561

An Effector Index to Predict Causal Genes at GWAS Loci

Forgetta, V.·Jiang, L.·Vulpescu, N. A.·Hogan, M. S.·Chen, S.·Morris, J. A.·Grinek, S.·Benner, C.·Mccarthy, M. I.·Fauman, E.·Greenwood, C. M.·Maurano, M. T.·Richards, J. B.

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Abstract

Drug development and biological discovery require effective strategies to map existing genetic associations to causal genes. To approach this problem, we began by identifying a set of positive control genes for 12 common diseases and traits that cause a Mendelian form of the disease or are the target of a medicine used for disease treatment. We then identified a widely-available set of genomic features enriching GWAS-associated single nucleotide variants (SNVs) for these positive control genes. Using these features, we trained and validated the Effector Index (Ei), a causal gene mapping algorithm using the 12 common diseases and traits. The area under Eis receiver operator curve to identify positive control genes was 80% and area under the precision recall curve was 29%. Using an enlarged set of independently curated positive control genes for type 2 diabetes which included genes identified by large-scale exome sequencing, these areas increased to 85% and 61%, respectively. The best predictors were coding or transcript altering SNVs, distance to gene and open chromatin-based metrics. We provide the Ei algorithm for its widespread use and have created a web-portal to facilitate understanding of results. This work outlines a simple, understandable approach to prioritize genes at GWAS loci for functional follow-up and drug development. Author summaryIn order to derive biological insight, or develop drugs based on genome-wide association studies (GWAS) data, causal genes at associated loci need to be identified. GWAS usually identify large genome regions containing many genes, but seldomly identifies specific causal genes. We have developed an algorithm to predict which genes in a region of disease association are likely causal and have named this algorithm the Effector Index. The Effector Index was optimized on diseases that have known causal or drug target genes, and further validated to predict these types of genes in independent datasets. The Effector Index formalizes these predictive features into a tool that can be used by researchers, and results from the traits and diseases studied here are available via the Accelerating Medicine Partnership web-portal at http://hugeamp.org/effectorgenes.html.

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Forgetta, V., Jiang, L., Vulpescu, N. A., Hogan, M. S., Chen, S., Morris, J. A., Grinek, S., Benner, C., Mccarthy, M. I., Fauman, E., Greenwood, C. M., Maurano, M. T., Richards, J. B.. 2020-06-28. An Effector Index to Predict Causal Genes at GWAS Loci. https://doi.org/10.1101/2020.06.28.171561

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