Cargando…
High-Sensitivity Transcriptome Data Structure and Implications for Analysis and Biologic Interpretation
Novel microarray technologies such as the AB1700 platform from Applied Biosystems promise significant increases in the signal dynamic range and a higher sensitivity for weakly expressed transcripts. We have compared a representative set of AB1700 data with a similarly representative Affymetrix HG-U1...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2006
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054080/ https://www.ncbi.nlm.nih.gov/pubmed/17531797 http://dx.doi.org/10.1016/S1672-0229(07)60002-3 |
_version_ | 1782458521761087488 |
---|---|
author | Noth, Sebastian Brysbaert, Guillaume Pellay, François-Xavier Benecke, Arndt |
author_facet | Noth, Sebastian Brysbaert, Guillaume Pellay, François-Xavier Benecke, Arndt |
author_sort | Noth, Sebastian |
collection | PubMed |
description | Novel microarray technologies such as the AB1700 platform from Applied Biosystems promise significant increases in the signal dynamic range and a higher sensitivity for weakly expressed transcripts. We have compared a representative set of AB1700 data with a similarly representative Affymetrix HG-U133A dataset. The AB1700 design extends the signal dynamic detection range at the lower bound by one order of magnitude. The lognormal signal distribution profiles of these high-sensitivity data need to be represented by two independent distributions. The additional second distribution covers those transcripts that would have gone undetected using the Affymetrix technology. The signal-dependent variance distribution in the AB1700 data is a non-trivial function of signal intensity, describable using a composite function. The drastically different structure of these high-sensitivity transcriptome profiles requires adaptation or even redevelopment of the standard microarray analysis methods. Based on the statistical properties, we have derived a signal variance distribution model for AB1700 data that is necessary for such development. Interestingly, the dual lognormal distribution observed in the AB1700 data reflects two fundamentally different biologic mechanisms of transcription initiation. |
format | Online Article Text |
id | pubmed-5054080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-50540802016-10-14 High-Sensitivity Transcriptome Data Structure and Implications for Analysis and Biologic Interpretation Noth, Sebastian Brysbaert, Guillaume Pellay, François-Xavier Benecke, Arndt Genomics Proteomics Bioinformatics Article Novel microarray technologies such as the AB1700 platform from Applied Biosystems promise significant increases in the signal dynamic range and a higher sensitivity for weakly expressed transcripts. We have compared a representative set of AB1700 data with a similarly representative Affymetrix HG-U133A dataset. The AB1700 design extends the signal dynamic detection range at the lower bound by one order of magnitude. The lognormal signal distribution profiles of these high-sensitivity data need to be represented by two independent distributions. The additional second distribution covers those transcripts that would have gone undetected using the Affymetrix technology. The signal-dependent variance distribution in the AB1700 data is a non-trivial function of signal intensity, describable using a composite function. The drastically different structure of these high-sensitivity transcriptome profiles requires adaptation or even redevelopment of the standard microarray analysis methods. Based on the statistical properties, we have derived a signal variance distribution model for AB1700 data that is necessary for such development. Interestingly, the dual lognormal distribution observed in the AB1700 data reflects two fundamentally different biologic mechanisms of transcription initiation. Elsevier 2006 2007-05-23 /pmc/articles/PMC5054080/ /pubmed/17531797 http://dx.doi.org/10.1016/S1672-0229(07)60002-3 Text en © 2006 Beijing Institute of Genomics http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open access article under the CC BY-NC-SA license (http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Article Noth, Sebastian Brysbaert, Guillaume Pellay, François-Xavier Benecke, Arndt High-Sensitivity Transcriptome Data Structure and Implications for Analysis and Biologic Interpretation |
title | High-Sensitivity Transcriptome Data Structure and Implications for Analysis and Biologic Interpretation |
title_full | High-Sensitivity Transcriptome Data Structure and Implications for Analysis and Biologic Interpretation |
title_fullStr | High-Sensitivity Transcriptome Data Structure and Implications for Analysis and Biologic Interpretation |
title_full_unstemmed | High-Sensitivity Transcriptome Data Structure and Implications for Analysis and Biologic Interpretation |
title_short | High-Sensitivity Transcriptome Data Structure and Implications for Analysis and Biologic Interpretation |
title_sort | high-sensitivity transcriptome data structure and implications for analysis and biologic interpretation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054080/ https://www.ncbi.nlm.nih.gov/pubmed/17531797 http://dx.doi.org/10.1016/S1672-0229(07)60002-3 |
work_keys_str_mv | AT nothsebastian highsensitivitytranscriptomedatastructureandimplicationsforanalysisandbiologicinterpretation AT brysbaertguillaume highsensitivitytranscriptomedatastructureandimplicationsforanalysisandbiologicinterpretation AT pellayfrancoisxavier highsensitivitytranscriptomedatastructureandimplicationsforanalysisandbiologicinterpretation AT beneckearndt highsensitivitytranscriptomedatastructureandimplicationsforanalysisandbiologicinterpretation |