Single-cell gene regulatory network prediction by explainable AI

被引:22
|
作者
Keyl, Philipp [1 ,2 ,3 ]
Bischoff, Philip [1 ,2 ,3 ,4 ,5 ]
Dernbach, Gabriel [1 ,2 ,3 ,6 ]
Bockmayr, Michael [1 ,2 ,3 ,7 ,8 ]
Fritz, Rebecca [1 ,2 ,3 ]
Horst, David [1 ,2 ,3 ,5 ]
Bluethgen, Nils [1 ,2 ,3 ,9 ]
Montavon, Gregoire [6 ,10 ]
Mueller, Klaus-Robert [6 ,10 ,11 ,12 ]
Klauschen, Frederick [1 ,2 ,3 ,5 ,6 ,13 ,14 ]
机构
[1] Charite Univ Med Berlin, Inst Pathol, Charitepl 1, D-10117 Berlin, Germany
[2] Free Univ Berlin, Charitepl 1, D-10117 Berlin, Germany
[3] Humboldt Univ, Charitepl 1, D-10117 Berlin, Germany
[4] Charite Univ Med Berlin, Berlin Inst Hlth, Anna Louisa Karsch Str 2, D-10178 Berlin, Germany
[5] German Canc Res Ctr, German Canc Consortium DKTK, Berlin Partner Site, Berlin, Germany
[6] BIFOLD Berlin Inst Fdn Learning & Data, Berlin, Germany
[7] Univ Med Ctr Hamburg Eppendorf, Dept Pediat Hematol & Oncolog, Martinistr 52, D-20246 Hamburg, Germany
[8] Univ Med Ctr Hamburg Eppendorf, Mildred Scheel Canc Career Ctr HaTriCS4, Martinistr 52, D-20246 Hamburg, Germany
[9] Humboldt Univ, Free Univ Berlin, Inst Biol, Unter Linden 6, D-10099 Berlin, Germany
[10] Tech Univ Berlin, Machine Learning Grp, Marchstr 23, D-10587 Berlin, Germany
[11] Korea Univ, Dept Artificial Intelligence, Seoul 136713, South Korea
[12] Max Planck Inst Informat, Stuhlsatzenhausweg 4, D-66123 Saarbrucken, Germany
[13] Ludwig Maximilians Univ Munchen, Inst Pathol, Thalkirchner Str 36, D-80337 Munich, Germany
[14] German Canc Res Ctr, German Canc Consortium DKTK, Munich Partner Site, Munich, Germany
关键词
CANCER; HETEROGENEITY; EXPRESSION; MUTATIONS;
D O I
10.1093/nar/gkac1212
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The 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.
引用
收藏
页码:E20 / E20
页数:14
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