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Selecting Reliable mRNA Expression Measurements Across Platforms Improves Downstream Analysis
With increasing use of publicly available gene expression data sets, the quality of the expression data is a critical issue for downstream analysis, gene signature development, and cross-validation of data sets. Thus, identifying reliable expression measurements by leveraging multiple mRNA expressio...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Libertas Academica
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4863871/ https://www.ncbi.nlm.nih.gov/pubmed/27199546 http://dx.doi.org/10.4137/CIN.S38590 |
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author | Tong, Pan Diao, Lixia Shen, Li Li, Lerong Heymach, John Victor Girard, Luc Minna, John D. Coombes, Kevin R. Byers, Lauren Averett Wang, Jing |
author_facet | Tong, Pan Diao, Lixia Shen, Li Li, Lerong Heymach, John Victor Girard, Luc Minna, John D. Coombes, Kevin R. Byers, Lauren Averett Wang, Jing |
author_sort | Tong, Pan |
collection | PubMed |
description | With increasing use of publicly available gene expression data sets, the quality of the expression data is a critical issue for downstream analysis, gene signature development, and cross-validation of data sets. Thus, identifying reliable expression measurements by leveraging multiple mRNA expression platforms is an important analytical task. In this study, we propose a statistical framework for selecting reliable measurements between platforms by modeling the correlations of mRNA expression levels using a beta-mixture model. The model-based selection provides an effective and objective way to separate good probes from probes with low quality, thereby improving the efficiency and accuracy of the analysis. The proposed method can be used to compare two microarray technologies or microarray and RNA sequencing measurements. We tested the approach in two matched profiling data sets, using microarray gene expression measurements from the same samples profiled on both Affymetrix and Illumina platforms. We also applied the algorithm to mRNA expression data to compare Affymetrix microarray data with RNA sequencing measurements. The algorithm successfully identified probes/genes with reliable measurements. Removing the unreliable measurements resulted in significant improvements for gene signature development and functional annotations. |
format | Online Article Text |
id | pubmed-4863871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Libertas Academica |
record_format | MEDLINE/PubMed |
spelling | pubmed-48638712016-05-19 Selecting Reliable mRNA Expression Measurements Across Platforms Improves Downstream Analysis Tong, Pan Diao, Lixia Shen, Li Li, Lerong Heymach, John Victor Girard, Luc Minna, John D. Coombes, Kevin R. Byers, Lauren Averett Wang, Jing Cancer Inform Original Research With increasing use of publicly available gene expression data sets, the quality of the expression data is a critical issue for downstream analysis, gene signature development, and cross-validation of data sets. Thus, identifying reliable expression measurements by leveraging multiple mRNA expression platforms is an important analytical task. In this study, we propose a statistical framework for selecting reliable measurements between platforms by modeling the correlations of mRNA expression levels using a beta-mixture model. The model-based selection provides an effective and objective way to separate good probes from probes with low quality, thereby improving the efficiency and accuracy of the analysis. The proposed method can be used to compare two microarray technologies or microarray and RNA sequencing measurements. We tested the approach in two matched profiling data sets, using microarray gene expression measurements from the same samples profiled on both Affymetrix and Illumina platforms. We also applied the algorithm to mRNA expression data to compare Affymetrix microarray data with RNA sequencing measurements. The algorithm successfully identified probes/genes with reliable measurements. Removing the unreliable measurements resulted in significant improvements for gene signature development and functional annotations. Libertas Academica 2016-05-10 /pmc/articles/PMC4863871/ /pubmed/27199546 http://dx.doi.org/10.4137/CIN.S38590 Text en © 2016 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 license. |
spellingShingle | Original Research Tong, Pan Diao, Lixia Shen, Li Li, Lerong Heymach, John Victor Girard, Luc Minna, John D. Coombes, Kevin R. Byers, Lauren Averett Wang, Jing Selecting Reliable mRNA Expression Measurements Across Platforms Improves Downstream Analysis |
title | Selecting Reliable mRNA Expression Measurements Across Platforms Improves Downstream Analysis |
title_full | Selecting Reliable mRNA Expression Measurements Across Platforms Improves Downstream Analysis |
title_fullStr | Selecting Reliable mRNA Expression Measurements Across Platforms Improves Downstream Analysis |
title_full_unstemmed | Selecting Reliable mRNA Expression Measurements Across Platforms Improves Downstream Analysis |
title_short | Selecting Reliable mRNA Expression Measurements Across Platforms Improves Downstream Analysis |
title_sort | selecting reliable mrna expression measurements across platforms improves downstream analysis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4863871/ https://www.ncbi.nlm.nih.gov/pubmed/27199546 http://dx.doi.org/10.4137/CIN.S38590 |
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