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Genome-wide estimation of transcript concentrations from spotted cDNA microarray data
A method providing absolute transcript concentrations from spotted microarray intensity data is presented. Number of transcripts per µg total RNA, mRNA or per cell, are obtained for each gene, enabling comparisons of transcript levels within and between tissues. The method is based on Bayesian stati...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1243803/ https://www.ncbi.nlm.nih.gov/pubmed/16204447 http://dx.doi.org/10.1093/nar/gni141 |
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author | Frigessi, Arnoldo van de Wiel, Mark A. Holden, Marit Svendsrud, Debbie H. Glad, Ingrid K. Lyng, Heidi |
author_facet | Frigessi, Arnoldo van de Wiel, Mark A. Holden, Marit Svendsrud, Debbie H. Glad, Ingrid K. Lyng, Heidi |
author_sort | Frigessi, Arnoldo |
collection | PubMed |
description | A method providing absolute transcript concentrations from spotted microarray intensity data is presented. Number of transcripts per µg total RNA, mRNA or per cell, are obtained for each gene, enabling comparisons of transcript levels within and between tissues. The method is based on Bayesian statistical modelling incorporating available information about the experiment from target preparation to image analysis, leading to realistically large confidence intervals for estimated concentrations. The method was validated in experiments using transcripts at known concentrations, showing accuracy and reproducibility of estimated concentrations, which were also in excellent agreement with results from quantitative real-time PCR. We determined the concentration for 10 157 genes in cervix cancers and a pool of cancer cell lines and found values in the range of 10(5)–10(10) transcripts per µg total RNA. The precision of our estimates was sufficiently high to detect significant concentration differences between two tumours and between different genes within the same tumour, comparisons that are not possible with standard intensity ratios. Our method can be used to explore the regulation of pathways and to develop individualized therapies, based on absolute transcript concentrations. It can be applied broadly, facilitating the construction of the transcriptome, continuously updating it by integrating future data. |
format | Text |
id | pubmed-1243803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-12438032005-10-07 Genome-wide estimation of transcript concentrations from spotted cDNA microarray data Frigessi, Arnoldo van de Wiel, Mark A. Holden, Marit Svendsrud, Debbie H. Glad, Ingrid K. Lyng, Heidi Nucleic Acids Res Methods Online A method providing absolute transcript concentrations from spotted microarray intensity data is presented. Number of transcripts per µg total RNA, mRNA or per cell, are obtained for each gene, enabling comparisons of transcript levels within and between tissues. The method is based on Bayesian statistical modelling incorporating available information about the experiment from target preparation to image analysis, leading to realistically large confidence intervals for estimated concentrations. The method was validated in experiments using transcripts at known concentrations, showing accuracy and reproducibility of estimated concentrations, which were also in excellent agreement with results from quantitative real-time PCR. We determined the concentration for 10 157 genes in cervix cancers and a pool of cancer cell lines and found values in the range of 10(5)–10(10) transcripts per µg total RNA. The precision of our estimates was sufficiently high to detect significant concentration differences between two tumours and between different genes within the same tumour, comparisons that are not possible with standard intensity ratios. Our method can be used to explore the regulation of pathways and to develop individualized therapies, based on absolute transcript concentrations. It can be applied broadly, facilitating the construction of the transcriptome, continuously updating it by integrating future data. Oxford University Press 2005 2005-10-04 /pmc/articles/PMC1243803/ /pubmed/16204447 http://dx.doi.org/10.1093/nar/gni141 Text en © The Author 2005. Published by Oxford University Press. All rights reserved |
spellingShingle | Methods Online Frigessi, Arnoldo van de Wiel, Mark A. Holden, Marit Svendsrud, Debbie H. Glad, Ingrid K. Lyng, Heidi Genome-wide estimation of transcript concentrations from spotted cDNA microarray data |
title | Genome-wide estimation of transcript concentrations from spotted cDNA microarray data |
title_full | Genome-wide estimation of transcript concentrations from spotted cDNA microarray data |
title_fullStr | Genome-wide estimation of transcript concentrations from spotted cDNA microarray data |
title_full_unstemmed | Genome-wide estimation of transcript concentrations from spotted cDNA microarray data |
title_short | Genome-wide estimation of transcript concentrations from spotted cDNA microarray data |
title_sort | genome-wide estimation of transcript concentrations from spotted cdna microarray data |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1243803/ https://www.ncbi.nlm.nih.gov/pubmed/16204447 http://dx.doi.org/10.1093/nar/gni141 |
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