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Probe set filtering increases correlation between Affymetrix GeneChip and qRT-PCR expression measurements
BACKGROUND: Affymetrix GeneChip microarrays are popular platforms for expression profiling in two types of studies: detection of differential expression computed by p-values of t-test and estimation of fold change between analyzed groups. There are many different preprocessing algorithms for summari...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841208/ https://www.ncbi.nlm.nih.gov/pubmed/20181266 http://dx.doi.org/10.1186/1471-2105-11-104 |
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author | Mieczkowski, Jakub Tyburczy, Magdalena E Dabrowski, Michal Pokarowski, Piotr |
author_facet | Mieczkowski, Jakub Tyburczy, Magdalena E Dabrowski, Michal Pokarowski, Piotr |
author_sort | Mieczkowski, Jakub |
collection | PubMed |
description | BACKGROUND: Affymetrix GeneChip microarrays are popular platforms for expression profiling in two types of studies: detection of differential expression computed by p-values of t-test and estimation of fold change between analyzed groups. There are many different preprocessing algorithms for summarizing Affymetrix data. The main goal of these methods is to remove effects of non-specific hybridization, and to optimally combine information from multiple probes annotated to the same transcript. The methods are benchmarked by comparison with reference methods, such as quantitative reverse-transcription PCR (qRT-PCR). RESULTS: We present a comprehensive analysis of agreement between Affymetrix GeneChip and qRT-PCR results. We analyzed the influence of filtering by fraction Present calls introduced by J.N. McClintick and H.J. Edenberg (2006) and 2 mapping procedures: updated probe sets definitions proposed by Dai et al. (2005) and our "naive mapping" method. Because of evolution of genome sequence annotations since the time when microarrays were designed, we also studied the effect of the annotation release date. These comparisons were prepared for 6 popular preprocessing algorithms (MAS5, PLIER, RMA, GC-RMA, MBEI, and MBEImm) in the 2 above-mentioned types of studies. We used data sets from 6 independent biological experiments. As a measure of reproducibility of microarray and qRT-PCR values, we used linear and rank correlation coefficients. CONCLUSIONS: We show that filtering by fraction Present calls increased correlations for all 6 preprocessing algorithms. We observed the difference in performance of PM-MM and PM-only methods: using MM probes increased correlations in fold change studies, but PM-only methods proved to perform better in detection of differential expression. We recommend using GC-RMA for detection of differential expression and PLIER for estimation of fold change. The use of the more recent annotation improves the results in both types of studies, encouraging re-analysis of old data. |
format | Text |
id | pubmed-2841208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28412082010-03-18 Probe set filtering increases correlation between Affymetrix GeneChip and qRT-PCR expression measurements Mieczkowski, Jakub Tyburczy, Magdalena E Dabrowski, Michal Pokarowski, Piotr BMC Bioinformatics Methodology article BACKGROUND: Affymetrix GeneChip microarrays are popular platforms for expression profiling in two types of studies: detection of differential expression computed by p-values of t-test and estimation of fold change between analyzed groups. There are many different preprocessing algorithms for summarizing Affymetrix data. The main goal of these methods is to remove effects of non-specific hybridization, and to optimally combine information from multiple probes annotated to the same transcript. The methods are benchmarked by comparison with reference methods, such as quantitative reverse-transcription PCR (qRT-PCR). RESULTS: We present a comprehensive analysis of agreement between Affymetrix GeneChip and qRT-PCR results. We analyzed the influence of filtering by fraction Present calls introduced by J.N. McClintick and H.J. Edenberg (2006) and 2 mapping procedures: updated probe sets definitions proposed by Dai et al. (2005) and our "naive mapping" method. Because of evolution of genome sequence annotations since the time when microarrays were designed, we also studied the effect of the annotation release date. These comparisons were prepared for 6 popular preprocessing algorithms (MAS5, PLIER, RMA, GC-RMA, MBEI, and MBEImm) in the 2 above-mentioned types of studies. We used data sets from 6 independent biological experiments. As a measure of reproducibility of microarray and qRT-PCR values, we used linear and rank correlation coefficients. CONCLUSIONS: We show that filtering by fraction Present calls increased correlations for all 6 preprocessing algorithms. We observed the difference in performance of PM-MM and PM-only methods: using MM probes increased correlations in fold change studies, but PM-only methods proved to perform better in detection of differential expression. We recommend using GC-RMA for detection of differential expression and PLIER for estimation of fold change. The use of the more recent annotation improves the results in both types of studies, encouraging re-analysis of old data. BioMed Central 2010-02-24 /pmc/articles/PMC2841208/ /pubmed/20181266 http://dx.doi.org/10.1186/1471-2105-11-104 Text en Copyright ©2010 Mieczkowski et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology article Mieczkowski, Jakub Tyburczy, Magdalena E Dabrowski, Michal Pokarowski, Piotr Probe set filtering increases correlation between Affymetrix GeneChip and qRT-PCR expression measurements |
title | Probe set filtering increases correlation between Affymetrix GeneChip and qRT-PCR expression measurements |
title_full | Probe set filtering increases correlation between Affymetrix GeneChip and qRT-PCR expression measurements |
title_fullStr | Probe set filtering increases correlation between Affymetrix GeneChip and qRT-PCR expression measurements |
title_full_unstemmed | Probe set filtering increases correlation between Affymetrix GeneChip and qRT-PCR expression measurements |
title_short | Probe set filtering increases correlation between Affymetrix GeneChip and qRT-PCR expression measurements |
title_sort | probe set filtering increases correlation between affymetrix genechip and qrt-pcr expression measurements |
topic | Methodology article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841208/ https://www.ncbi.nlm.nih.gov/pubmed/20181266 http://dx.doi.org/10.1186/1471-2105-11-104 |
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