Literature DB >> 34296082

DeepCOMBI: explainable artificial intelligence for the analysis and discovery in genome-wide association studies.

Bettina Mieth1, Alexandre Rozier1, Juan Antonio Rodriguez2, Marina M C Höhne1, Nico Görnitz3, Klaus-Robert Müller1.   

Abstract

Deep learning has revolutionized data science in many fields by greatly improving prediction performances in comparison to conventional approaches. Recently, explainable artificial intelligence has emerged as an area of research that goes beyond pure prediction improvement by extracting knowledge from deep learning methodologies through the interpretation of their results. We investigate such explanations to explore the genetic architectures of phenotypes in genome-wide association studies. Instead of testing each position in the genome individually, the novel three-step algorithm, called DeepCOMBI, first trains a neural network for the classification of subjects into their respective phenotypes. Second, it explains the classifiers' decisions by applying layer-wise relevance propagation as one example from the pool of explanation techniques. The resulting importance scores are eventually used to determine a subset of the most relevant locations for multiple hypothesis testing in the third step. The performance of DeepCOMBI in terms of power and precision is investigated on generated datasets and a 2007 study. Verification of the latter is achieved by validating all findings with independent studies published up until 2020. DeepCOMBI is shown to outperform ordinary raw P-value thresholding and other baseline methods. Two novel disease associations (rs10889923 for hypertension, rs4769283 for type 1 diabetes) were identified.
© The Author(s) 2021. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics.

Entities:  

Year:  2021        PMID: 34296082      PMCID: PMC8291080          DOI: 10.1093/nargab/lqab065

Source DB:  PubMed          Journal:  NAR Genom Bioinform        ISSN: 2631-9268


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