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.

Details

Title
DeepCOMBI: explainable artificial intelligence for the analysis and discovery in genome-wide association studies
Author
Mieth, Bettina 1   VIAFID ORCID Logo  ; Rozier, Alexandre 1 ; Rodriguez, Juan Antonio 2 ; Höhne, Marina M C 1 ; Görnitz, Nico 3 ; Klaus-Robert Müller 1 

 Machine Learning Group, Technische Universität Berlin , Berlin 10587, Germany 
 CNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST) , Barcelona 08003, Spain 
 123ai.de , Berlin 10319, Germany 
Publication year
2021
Publication date
Sep 2021
Publisher
Oxford University Press
e-ISSN
26319268
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3170915681
Copyright
© The Author(s) 2021. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.