Comprehensive evaluation of transcriptome-based cell-type quantification methods for immuno-oncology

Author:

Sturm Gregor12,Finotello Francesca3,Petitprez Florent45,Zhang Jitao David6,Baumbach Jan1,Fridman Wolf H4,List Markus7,Aneichyk Tatsiana28

Affiliation:

1. Chair of Experimental Bioinformatics, TUM School of Life Sciences Weihenstephan, Technical University of Munich, Freising, Germany

2. Pieris Pharmaceuticals GmbH, Freising, Germany

3. Biocenter, Division of Bioinformatics, Medical University of Innsbruck, Innsbruck, Austria

4. Cordeliers Research Centre, UMRS_1138, INSERM, University Paris-Descartes, Sorbonne University, Paris, France

5. Programme Cartes d’Identité des Tumeurs, Ligue Nationale Contre le Cancer, Paris, France

6. Roche Pharma Research and Early Development, Pharmaceutical Sciences, Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd, Basel, Switzerland

7. Big Data in BioMedicine Group, Chair of Experimental Bioinformatis, TUM School of Life Sciences Weihenstephan, Technical University of Munich, Freising, Germany

8. Independent Data Lab UG, Munich, Germany

Abstract

Abstract Motivation The composition and density of immune cells in the tumor microenvironment (TME) profoundly influence tumor progression and success of anti-cancer therapies. Flow cytometry, immunohistochemistry staining or single-cell sequencing are often unavailable such that we rely on computational methods to estimate the immune-cell composition from bulk RNA-sequencing (RNA-seq) data. Various methods have been proposed recently, yet their capabilities and limitations have not been evaluated systematically. A general guideline leading the research community through cell type deconvolution is missing. Results We developed a systematic approach for benchmarking such computational methods and assessed the accuracy of tools at estimating nine different immune- and stromal cells from bulk RNA-seq samples. We used a single-cell RNA-seq dataset of ∼11 000 cells from the TME to simulate bulk samples of known cell type proportions, and validated the results using independent, publicly available gold-standard estimates. This allowed us to analyze and condense the results of more than a hundred thousand predictions to provide an exhaustive evaluation across seven computational methods over nine cell types and ∼1800 samples from five simulated and real-world datasets. We demonstrate that computational deconvolution performs at high accuracy for well-defined cell-type signatures and propose how fuzzy cell-type signatures can be improved. We suggest that future efforts should be dedicated to refining cell population definitions and finding reliable signatures. Availability and implementation A snakemake pipeline to reproduce the benchmark is available at https://github.com/grst/immune_deconvolution_benchmark. An R package allows the community to perform integrated deconvolution using different methods (https://grst.github.io/immunedeconv). Supplementary information Supplementary data are available at Bioinformatics online.

Funder

Austrian Cancer Aid

Austrian Science Fund

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

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