Deep neural network learning biological condition information refines gene-expression-based cell subtypes

Author:

Fan Zhenjiang1,Sun Jie2,Thorpe Henry3,Lee Stephen1,Kim Soyeon4567,Park Hyun Jung2ORCID

Affiliation:

1. Department of Computer Science, University of Pittsburgh , Pittsburgh, Pennsylvania 15213 , United States

2. Department of Human Genetics, University of Pittsburgh , Pittsburgh, Pennsylvania 15213 , United States

3. Department of Biostatistics, University of Pittsburgh , Pittsburgh, Pennsylvania 15213 , United States

4. Division of Pulmonary Medicine , Department of Pediatrics, UPMC Children’s Hospital of Pittsburgh, , Pittsburgh, PA , USA

5. University of Pittsburgh , Department of Pediatrics, UPMC Children’s Hospital of Pittsburgh, , Pittsburgh, PA , USA

6. Department of Pediatrics , School of Medicine, , Pittsburgh, PA , USA

7. University of Pittsburgh , School of Medicine, , Pittsburgh, PA , USA

Abstract

Abstract With the recent advent of single-cell level biological understanding, a growing interest is in identifying cell states or subtypes that are homogeneous in terms of gene expression and are also enriched in certain biological conditions, including disease samples versus normal samples (condition-specific cell subtype). Despite the importance of identifying condition-specific cell subtypes, existing methods have the following limitations: since they train models separately between gene expression and the biological condition information, (1) they do not consider potential interactions between them, and (2) the weights from both types of information are not properly controlled. Also, (3) they do not consider non-linear relationships in the gene expression and the biological condition. To address the limitations and accurately identify such condition-specific cell subtypes, we develop scDeepJointClust, the first method that jointly trains both types of information via a deep neural network. scDeepJointClust incorporates results from the power of state-of-the-art gene-expression-based clustering methods as an input, incorporating their sophistication and accuracy. We evaluated scDeepJointClust on both simulation data in diverse scenarios and biological data of different diseases (melanoma and non-small-cell lung cancer) and showed that scDeepJointClust outperforms existing methods in terms of sensitivity and specificity. scDeepJointClust exhibits significant promise in advancing our understanding of cellular states and their implications in complex biological systems.

Funder

UPMC Hillman Cancer Center Biostatistics Shared Resource

National Institutes of Health

Hillman Cancer Center Career Enhancement Program

Publisher

Oxford University Press (OUP)

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