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Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells
A goal of cancer research is to reveal cell subsets linked to continuous clinical outcomes to generate new therapeutic and biomarker hypotheses. We introduce a machine learning algorithm, Risk Assessment Population IDentification (RAPID), that is unsupervised and automated, identifies phenotypically...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7340505/ https://www.ncbi.nlm.nih.gov/pubmed/32573435 http://dx.doi.org/10.7554/eLife.56879 |
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author | Leelatian, Nalin Sinnaeve, Justine Mistry, Akshitkumar M Barone, Sierra M Brockman, Asa A Diggins, Kirsten E Greenplate, Allison R Weaver, Kyle D Thompson, Reid C Chambless, Lola B Mobley, Bret C Ihrie, Rebecca A Irish, Jonathan M |
author_facet | Leelatian, Nalin Sinnaeve, Justine Mistry, Akshitkumar M Barone, Sierra M Brockman, Asa A Diggins, Kirsten E Greenplate, Allison R Weaver, Kyle D Thompson, Reid C Chambless, Lola B Mobley, Bret C Ihrie, Rebecca A Irish, Jonathan M |
author_sort | Leelatian, Nalin |
collection | PubMed |
description | A goal of cancer research is to reveal cell subsets linked to continuous clinical outcomes to generate new therapeutic and biomarker hypotheses. We introduce a machine learning algorithm, Risk Assessment Population IDentification (RAPID), that is unsupervised and automated, identifies phenotypically distinct cell populations, and determines whether these populations stratify patient survival. With a pilot mass cytometry dataset of 2 million cells from 28 glioblastomas, RAPID identified tumor cells whose abundance independently and continuously stratified patient survival. Statistical validation within the workflow included repeated runs of stochastic steps and cell subsampling. Biological validation used an orthogonal platform, immunohistochemistry, and a larger cohort of 73 glioblastoma patients to confirm the findings from the pilot cohort. RAPID was also validated to find known risk stratifying cells and features using published data from blood cancer. Thus, RAPID provides an automated, unsupervised approach for finding statistically and biologically significant cells using cytometry data from patient samples. |
format | Online Article Text |
id | pubmed-7340505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-73405052020-07-13 Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells Leelatian, Nalin Sinnaeve, Justine Mistry, Akshitkumar M Barone, Sierra M Brockman, Asa A Diggins, Kirsten E Greenplate, Allison R Weaver, Kyle D Thompson, Reid C Chambless, Lola B Mobley, Bret C Ihrie, Rebecca A Irish, Jonathan M eLife Computational and Systems Biology A goal of cancer research is to reveal cell subsets linked to continuous clinical outcomes to generate new therapeutic and biomarker hypotheses. We introduce a machine learning algorithm, Risk Assessment Population IDentification (RAPID), that is unsupervised and automated, identifies phenotypically distinct cell populations, and determines whether these populations stratify patient survival. With a pilot mass cytometry dataset of 2 million cells from 28 glioblastomas, RAPID identified tumor cells whose abundance independently and continuously stratified patient survival. Statistical validation within the workflow included repeated runs of stochastic steps and cell subsampling. Biological validation used an orthogonal platform, immunohistochemistry, and a larger cohort of 73 glioblastoma patients to confirm the findings from the pilot cohort. RAPID was also validated to find known risk stratifying cells and features using published data from blood cancer. Thus, RAPID provides an automated, unsupervised approach for finding statistically and biologically significant cells using cytometry data from patient samples. eLife Sciences Publications, Ltd 2020-06-23 /pmc/articles/PMC7340505/ /pubmed/32573435 http://dx.doi.org/10.7554/eLife.56879 Text en © 2020, Leelatian et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Leelatian, Nalin Sinnaeve, Justine Mistry, Akshitkumar M Barone, Sierra M Brockman, Asa A Diggins, Kirsten E Greenplate, Allison R Weaver, Kyle D Thompson, Reid C Chambless, Lola B Mobley, Bret C Ihrie, Rebecca A Irish, Jonathan M Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells |
title | Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells |
title_full | Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells |
title_fullStr | Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells |
title_full_unstemmed | Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells |
title_short | Unsupervised machine learning reveals risk stratifying glioblastoma tumor cells |
title_sort | unsupervised machine learning reveals risk stratifying glioblastoma tumor cells |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7340505/ https://www.ncbi.nlm.nih.gov/pubmed/32573435 http://dx.doi.org/10.7554/eLife.56879 |
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