Deep learning predicts gene expression as an intermediate data modality to identify susceptibility patterns in Mycobacterium tuberculosis infected Diversity Outbred mice.

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Abstract

Machine learning sustains successful application to many diagnostic and prognostic problems in computational histopathology. Yet, few efforts have been made to model gene expression from histopathology. This study proposes a methodology which predicts selected gene expression values (microarray) from haematoxylin and eosin whole-slide images as an intermediate data modality to identify fulminant-like pulmonary tuberculosis (‘supersusceptible’) in an experimentally infected cohort of Diversity Outbred mice (n=77).
Gradient-boosted trees were utilized as a novel feature selector to identify gene transcripts predictive of fulminant-like pulmonary tuberculosis. A novel attention-based multiple instance learning model for regression was used to predict selected genes’ expression from whole-slide images. Gene expression predictions were shown to be sufficiently replicated to identify supersusceptible mice using gradient-boosted trees trained on ground truth gene expression data.
The model was accurate, showing high positive correlations with ground truth gene expression on both cross-validation (nĀ =Ā 77, 0.63 ā‰¤ Ļ ā‰¤ 0.84) and external testing sets (nĀ =Ā 33, 0.65 ā‰¤ Ļ ā‰¤ 0.84). The sensitivity and specificity for gene expression predictions to identify supersusceptible mice (n=77) were 0.88 and 0.95, respectively, and for an external set of mice (n=33) 0.88 and 0.93, respectively.
Our methodology maps histopathology to gene expression with sufficient accuracy to predict a clinical outcome. The proposed methodology exemplifies a computational template for gene expression panels, in which relatively inexpensive and widely available tissue histopathology may be mapped to specific genes’ expression to serve as a diagnostic or prognostic tool.
National Institutes of Health and American Lung Association.
Copyright Ā© 2021 The Authors. Published by Elsevier B.V. All rights reserved.

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