DeCompress: tissue compartment deconvolution of targeted mRNA expression panels using compressed sensing

Author:

Bhattacharya Arjun1ORCID,Hamilton Alina M2,Troester Melissa A23,Love Michael I45

Affiliation:

1. Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, CA 90095, USA

2. Department of Pathology and Laboratory Medicine, University of North Carolina-Chapel Hill, Chapel Hill, NC 27516, USA

3. Department of Epidemiology, University of North Carolina-Chapel Hill, Chapel Hill, NC 27516, USA

4. Department of Biostatistics, University of North Carolina-Chapel Hill, Chapel Hill, NC 27516, USA

5. Department of Genetics, University of North Carolina-Chapel Hill, Chapel Hill, NC 27516, USA

Abstract

Abstract Targeted mRNA expression panels, measuring up to 800 genes, are used in academic and clinical settings due to low cost and high sensitivity for archived samples. Most samples assayed on targeted panels originate from bulk tissue comprised of many cell types, and cell-type heterogeneity confounds biological signals. Reference-free methods are used when cell-type-specific expression references are unavailable, but limited feature spaces render implementation challenging in targeted panels. Here, we present DeCompress, a semi-reference-free deconvolution method for targeted panels. DeCompress leverages a reference RNA-seq or microarray dataset from similar tissue to expand the feature space of targeted panels using compressed sensing. Ensemble reference-free deconvolution is performed on this artificially expanded dataset to estimate cell-type proportions and gene signatures. In simulated mixtures, four public cell line mixtures, and a targeted panel (1199 samples; 406 genes) from the Carolina Breast Cancer Study, DeCompress recapitulates cell-type proportions with less error than reference-free methods and finds biologically relevant compartments. We integrate compartment estimates into cis-eQTL mapping in breast cancer, identifying a tumor-specific cis-eQTL for CCR3 (C–C Motif Chemokine Receptor 3) at a risk locus. DeCompress improves upon reference-free methods without requiring expression profiles from pure cell populations, with applications in genomic analyses and clinical settings.

Funder

National Institutes of Health

National Cancer Institute

National Human Genome Research Institute

National Institute of Environmental Health Sciences

National Institute of General Medical Sciences

University of North Carolina at Chapel Hill

Publisher

Oxford University Press (OUP)

Subject

Genetics

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