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A score system for quality evaluation of RNA sequence tags: an improvement for gene expression profiling
BACKGROUND: High-throughput molecular approaches for gene expression profiling, such as Serial Analysis of Gene Expression (SAGE), Massively Parallel Signature Sequencing (MPSS) or Sequencing-by-Synthesis (SBS) represent powerful techniques that provide global transcription profiles of different cel...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2701951/ https://www.ncbi.nlm.nih.gov/pubmed/19500384 http://dx.doi.org/10.1186/1471-2105-10-170 |
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author | Pinheiro, Daniel G Galante, Pedro AF de Souza, Sandro J Zago, Marco A Silva, Wilson A |
author_facet | Pinheiro, Daniel G Galante, Pedro AF de Souza, Sandro J Zago, Marco A Silva, Wilson A |
author_sort | Pinheiro, Daniel G |
collection | PubMed |
description | BACKGROUND: High-throughput molecular approaches for gene expression profiling, such as Serial Analysis of Gene Expression (SAGE), Massively Parallel Signature Sequencing (MPSS) or Sequencing-by-Synthesis (SBS) represent powerful techniques that provide global transcription profiles of different cell types through sequencing of short fragments of transcripts, denominated sequence tags. These techniques have improved our understanding about the relationships between these expression profiles and cellular phenotypes. Despite this, more reliable datasets are still necessary. In this work, we present a web-based tool named S3T: Score System for Sequence Tags, to index sequenced tags in accordance with their reliability. This is made through a series of evaluations based on a defined rule set. S3T allows the identification/selection of tags, considered more reliable for further gene expression analysis. RESULTS: This methodology was applied to a public SAGE dataset. In order to compare data before and after filtering, a hierarchical clustering analysis was performed in samples from the same type of tissue, in distinct biological conditions, using these two datasets. Our results provide evidences suggesting that it is possible to find more congruous clusters after using S3T scoring system. CONCLUSION: These results substantiate the proposed application to generate more reliable data. This is a significant contribution for determination of global gene expression profiles. The library analysis with S3T is freely available at . S3T source code and datasets can also be downloaded from the aforementioned website. |
format | Text |
id | pubmed-2701951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27019512009-06-26 A score system for quality evaluation of RNA sequence tags: an improvement for gene expression profiling Pinheiro, Daniel G Galante, Pedro AF de Souza, Sandro J Zago, Marco A Silva, Wilson A BMC Bioinformatics Software BACKGROUND: High-throughput molecular approaches for gene expression profiling, such as Serial Analysis of Gene Expression (SAGE), Massively Parallel Signature Sequencing (MPSS) or Sequencing-by-Synthesis (SBS) represent powerful techniques that provide global transcription profiles of different cell types through sequencing of short fragments of transcripts, denominated sequence tags. These techniques have improved our understanding about the relationships between these expression profiles and cellular phenotypes. Despite this, more reliable datasets are still necessary. In this work, we present a web-based tool named S3T: Score System for Sequence Tags, to index sequenced tags in accordance with their reliability. This is made through a series of evaluations based on a defined rule set. S3T allows the identification/selection of tags, considered more reliable for further gene expression analysis. RESULTS: This methodology was applied to a public SAGE dataset. In order to compare data before and after filtering, a hierarchical clustering analysis was performed in samples from the same type of tissue, in distinct biological conditions, using these two datasets. Our results provide evidences suggesting that it is possible to find more congruous clusters after using S3T scoring system. CONCLUSION: These results substantiate the proposed application to generate more reliable data. This is a significant contribution for determination of global gene expression profiles. The library analysis with S3T is freely available at . S3T source code and datasets can also be downloaded from the aforementioned website. BioMed Central 2009-06-06 /pmc/articles/PMC2701951/ /pubmed/19500384 http://dx.doi.org/10.1186/1471-2105-10-170 Text en Copyright © 2009 Pinheiro 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 | Software Pinheiro, Daniel G Galante, Pedro AF de Souza, Sandro J Zago, Marco A Silva, Wilson A A score system for quality evaluation of RNA sequence tags: an improvement for gene expression profiling |
title | A score system for quality evaluation of RNA sequence tags: an improvement for gene expression profiling |
title_full | A score system for quality evaluation of RNA sequence tags: an improvement for gene expression profiling |
title_fullStr | A score system for quality evaluation of RNA sequence tags: an improvement for gene expression profiling |
title_full_unstemmed | A score system for quality evaluation of RNA sequence tags: an improvement for gene expression profiling |
title_short | A score system for quality evaluation of RNA sequence tags: an improvement for gene expression profiling |
title_sort | score system for quality evaluation of rna sequence tags: an improvement for gene expression profiling |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2701951/ https://www.ncbi.nlm.nih.gov/pubmed/19500384 http://dx.doi.org/10.1186/1471-2105-10-170 |
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