Single-cell gene regulatory network prediction by explainable AI

Author:

Keyl Philipp1ORCID,Bischoff Philip123,Dernbach Gabriel14,Bockmayr Michael156,Fritz Rebecca1,Horst David13,Blüthgen Nils17ORCID,Montavon Grégoire48,Müller Klaus-Robert48910ORCID,Klauschen Frederick1341112

Affiliation:

1. Institute of Pathology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität Berlin , Charitéplatz 1, 10117 Berlin, Germany

2. Berlin Institute of Health at Charité - Universitätsmedizin Berlin , Anna-Louisa-Karsch-Straße 2, 10178 Berlin, Germany

3. German Cancer Consortium (DKTK), German Cancer Research Center (DKFZ) , Berlin partner site, Germany

4. BIFOLD – Berlin Institute for the Foundations of Learning and Data , Berlin, Germany

5. Department of Pediatric Hematology and Oncolog, University Medical Center Hamburg-Eppendorf , Martinistr. 52, 20246 Hamburg, Germany

6. Mildred Scheel Cancer Career Center HaTriCS4 , University Medical Center Hamburg-Eppendorf Martinistr. 52, 20246 Hamburg, Germany

7. Institut für Biologie, Humboldt University, Free University of Berlin , Unter den Linden 6, 10099 Berlin, Germany

8. Machine Learning Group, Technical University of Berlin , Marchstr. 23, 10587 Berlin, Germany

9. Department of Artificial Intelligence, Korea University , Seoul 136-713, South Korea

10. Max-Planck-Institute for Informatics , Stuhlsatzenhausweg 4, 66123 Saarbrücken, Germany

11. Institute of Pathology, Ludwig-Maximilians-University Munich , Thalkirchner Str. 36, 80337 München, Germany

12. German Cancer Consortium (DKTK), German Cancer Research Center (DKFZ) , Munich partner site, Germany

Abstract

AbstractThe molecular heterogeneity of cancer cells contributes to the often partial response to targeted therapies and relapse of disease due to the escape of resistant cell populations. While single-cell sequencing has started to improve our understanding of this heterogeneity, it offers a mostly descriptive view on cellular types and states. To obtain more functional insights, we propose scGeneRAI, an explainable deep learning approach that uses layer-wise relevance propagation (LRP) to infer gene regulatory networks from static single-cell RNA sequencing data for individual cells. We benchmark our method with synthetic data and apply it to single-cell RNA sequencing data of a cohort of human lung cancers. From the predicted single-cell networks our approach reveals characteristic network patterns for tumor cells and normal epithelial cells and identifies subnetworks that are observed only in (subgroups of) tumor cells of certain patients. While current state-of-the-art methods are limited by their ability to only predict average networks for cell populations, our approach facilitates the reconstruction of networks down to the level of single cells which can be utilized to characterize the heterogeneity of gene regulation within and across tumors.

Funder

Charité – Universitätsmedizin Berlin

Berlin Institute of Health at Charité

IITP

Korea government

MSIT

Korea University

BMBF

Institute of Pathology, Munich

Publisher

Oxford University Press (OUP)

Subject

Genetics

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