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ISOpureR: an R implementation of a computational purification algorithm of mixed tumour profiles
BACKGROUND: Tumour samples containing distinct sub-populations of cancer and normal cells present challenges in the development of reproducible biomarkers, as these biomarkers are based on bulk signals from mixed tumour profiles. ISOpure is the only mRNA computational purification method to date tha...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429941/ https://www.ncbi.nlm.nih.gov/pubmed/25972088 http://dx.doi.org/10.1186/s12859-015-0597-x |
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author | Anghel, Catalina V Quon, Gerald Haider, Syed Nguyen, Francis Deshwar, Amit G Morris, Quaid D Boutros, Paul C |
author_facet | Anghel, Catalina V Quon, Gerald Haider, Syed Nguyen, Francis Deshwar, Amit G Morris, Quaid D Boutros, Paul C |
author_sort | Anghel, Catalina V |
collection | PubMed |
description | BACKGROUND: Tumour samples containing distinct sub-populations of cancer and normal cells present challenges in the development of reproducible biomarkers, as these biomarkers are based on bulk signals from mixed tumour profiles. ISOpure is the only mRNA computational purification method to date that does not require a paired tumour-normal sample, provides a personalized cancer profile for each patient, and has been tested on clinical data. Replacing mixed tumour profiles with ISOpure-preprocessed cancer profiles led to better prognostic gene signatures for lung and prostate cancer. RESULTS: To simplify the integration of ISOpure into standard R-based bioinformatics analysis pipelines, the algorithm has been implemented as an R package. The ISOpureR package performs analogously to the original code in estimating the fraction of cancer cells and the patient cancer mRNA abundance profile from tumour samples in four cancer datasets. CONCLUSIONS: The ISOpureR package estimates the fraction of cancer cells and personalized patient cancer mRNA abundance profile from a mixed tumour profile. This open-source R implementation enables integration into existing computational pipelines, as well as easy testing, modification and extension of the model. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-015-0597-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4429941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44299412015-05-14 ISOpureR: an R implementation of a computational purification algorithm of mixed tumour profiles Anghel, Catalina V Quon, Gerald Haider, Syed Nguyen, Francis Deshwar, Amit G Morris, Quaid D Boutros, Paul C BMC Bioinformatics Software BACKGROUND: Tumour samples containing distinct sub-populations of cancer and normal cells present challenges in the development of reproducible biomarkers, as these biomarkers are based on bulk signals from mixed tumour profiles. ISOpure is the only mRNA computational purification method to date that does not require a paired tumour-normal sample, provides a personalized cancer profile for each patient, and has been tested on clinical data. Replacing mixed tumour profiles with ISOpure-preprocessed cancer profiles led to better prognostic gene signatures for lung and prostate cancer. RESULTS: To simplify the integration of ISOpure into standard R-based bioinformatics analysis pipelines, the algorithm has been implemented as an R package. The ISOpureR package performs analogously to the original code in estimating the fraction of cancer cells and the patient cancer mRNA abundance profile from tumour samples in four cancer datasets. CONCLUSIONS: The ISOpureR package estimates the fraction of cancer cells and personalized patient cancer mRNA abundance profile from a mixed tumour profile. This open-source R implementation enables integration into existing computational pipelines, as well as easy testing, modification and extension of the model. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-015-0597-x) contains supplementary material, which is available to authorized users. BioMed Central 2015-05-14 /pmc/articles/PMC4429941/ /pubmed/25972088 http://dx.doi.org/10.1186/s12859-015-0597-x Text en © Anghel et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Software Anghel, Catalina V Quon, Gerald Haider, Syed Nguyen, Francis Deshwar, Amit G Morris, Quaid D Boutros, Paul C ISOpureR: an R implementation of a computational purification algorithm of mixed tumour profiles |
title | ISOpureR: an R implementation of a computational purification algorithm of mixed tumour profiles |
title_full | ISOpureR: an R implementation of a computational purification algorithm of mixed tumour profiles |
title_fullStr | ISOpureR: an R implementation of a computational purification algorithm of mixed tumour profiles |
title_full_unstemmed | ISOpureR: an R implementation of a computational purification algorithm of mixed tumour profiles |
title_short | ISOpureR: an R implementation of a computational purification algorithm of mixed tumour profiles |
title_sort | isopurer: an r implementation of a computational purification algorithm of mixed tumour profiles |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429941/ https://www.ncbi.nlm.nih.gov/pubmed/25972088 http://dx.doi.org/10.1186/s12859-015-0597-x |
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