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DeCompress: tissue compartment deconvolution of targeted mRNA expression panels using compressed sensing
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 bio...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096278/ https://www.ncbi.nlm.nih.gov/pubmed/33524140 http://dx.doi.org/10.1093/nar/gkab031 |
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author | Bhattacharya, Arjun Hamilton, Alina M Troester, Melissa A Love, Michael I |
author_facet | Bhattacharya, Arjun Hamilton, Alina M Troester, Melissa A Love, Michael I |
author_sort | Bhattacharya, Arjun |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8096278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-80962782021-05-10 DeCompress: tissue compartment deconvolution of targeted mRNA expression panels using compressed sensing Bhattacharya, Arjun Hamilton, Alina M Troester, Melissa A Love, Michael I Nucleic Acids Res Methods Online 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. Oxford University Press 2021-02-01 /pmc/articles/PMC8096278/ /pubmed/33524140 http://dx.doi.org/10.1093/nar/gkab031 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Methods Online Bhattacharya, Arjun Hamilton, Alina M Troester, Melissa A Love, Michael I DeCompress: tissue compartment deconvolution of targeted mRNA expression panels using compressed sensing |
title | DeCompress: tissue compartment deconvolution of targeted mRNA expression panels using compressed sensing |
title_full | DeCompress: tissue compartment deconvolution of targeted mRNA expression panels using compressed sensing |
title_fullStr | DeCompress: tissue compartment deconvolution of targeted mRNA expression panels using compressed sensing |
title_full_unstemmed | DeCompress: tissue compartment deconvolution of targeted mRNA expression panels using compressed sensing |
title_short | DeCompress: tissue compartment deconvolution of targeted mRNA expression panels using compressed sensing |
title_sort | decompress: tissue compartment deconvolution of targeted mrna expression panels using compressed sensing |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096278/ https://www.ncbi.nlm.nih.gov/pubmed/33524140 http://dx.doi.org/10.1093/nar/gkab031 |
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