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MSProGene: integrative proteogenomics beyond six-frames and single nucleotide polymorphisms
Summary: Ongoing advances in high-throughput technologies have facilitated accurate proteomic measurements and provide a wealth of information on genomic and transcript level. In proteogenomics, this multi-omics data is combined to analyze unannotated organisms and to allow more accurate sample-spec...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4765881/ https://www.ncbi.nlm.nih.gov/pubmed/26072472 http://dx.doi.org/10.1093/bioinformatics/btv236 |
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author | Zickmann, Franziska Renard, Bernhard Y. |
author_facet | Zickmann, Franziska Renard, Bernhard Y. |
author_sort | Zickmann, Franziska |
collection | PubMed |
description | Summary: Ongoing advances in high-throughput technologies have facilitated accurate proteomic measurements and provide a wealth of information on genomic and transcript level. In proteogenomics, this multi-omics data is combined to analyze unannotated organisms and to allow more accurate sample-specific predictions. Existing analysis methods still mainly depend on six-frame translations or reference protein databases that are extended by transcriptomic information or known single nucleotide polymorphisms (SNPs). However, six-frames introduce an artificial sixfold increase of the target database and SNP integration requires a suitable database summarizing results from previous experiments. We overcome these limitations by introducing MSProGene, a new method for integrative proteogenomic analysis based on customized RNA-Seq driven transcript databases. MSProGene is independent from existing reference databases or annotated SNPs and avoids large six-frame translated databases by constructing sample-specific transcripts. In addition, it creates a network combining RNA-Seq and peptide information that is optimized by a maximum-flow algorithm. It thereby also allows resolving the ambiguity of shared peptides for protein inference. We applied MSProGene on three datasets and show that it facilitates a database-independent reliable yet accurate prediction on gene and protein level and additionally identifies novel genes. Availability and implementation: MSProGene is written in Java and Python. It is open source and available at http://sourceforge.net/projects/msprogene/. Contact: renardb@rki.de |
format | Online Article Text |
id | pubmed-4765881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47658812016-03-04 MSProGene: integrative proteogenomics beyond six-frames and single nucleotide polymorphisms Zickmann, Franziska Renard, Bernhard Y. Bioinformatics Ismb/Eccb 2015 Proceedings Papers Committee July 10 to July 14, 2015, Dublin, Ireland Summary: Ongoing advances in high-throughput technologies have facilitated accurate proteomic measurements and provide a wealth of information on genomic and transcript level. In proteogenomics, this multi-omics data is combined to analyze unannotated organisms and to allow more accurate sample-specific predictions. Existing analysis methods still mainly depend on six-frame translations or reference protein databases that are extended by transcriptomic information or known single nucleotide polymorphisms (SNPs). However, six-frames introduce an artificial sixfold increase of the target database and SNP integration requires a suitable database summarizing results from previous experiments. We overcome these limitations by introducing MSProGene, a new method for integrative proteogenomic analysis based on customized RNA-Seq driven transcript databases. MSProGene is independent from existing reference databases or annotated SNPs and avoids large six-frame translated databases by constructing sample-specific transcripts. In addition, it creates a network combining RNA-Seq and peptide information that is optimized by a maximum-flow algorithm. It thereby also allows resolving the ambiguity of shared peptides for protein inference. We applied MSProGene on three datasets and show that it facilitates a database-independent reliable yet accurate prediction on gene and protein level and additionally identifies novel genes. Availability and implementation: MSProGene is written in Java and Python. It is open source and available at http://sourceforge.net/projects/msprogene/. Contact: renardb@rki.de Oxford University Press 2015-06-15 2015-06-10 /pmc/articles/PMC4765881/ /pubmed/26072472 http://dx.doi.org/10.1093/bioinformatics/btv236 Text en © The Author 2015. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Ismb/Eccb 2015 Proceedings Papers Committee July 10 to July 14, 2015, Dublin, Ireland Zickmann, Franziska Renard, Bernhard Y. MSProGene: integrative proteogenomics beyond six-frames and single nucleotide polymorphisms |
title | MSProGene: integrative proteogenomics beyond six-frames and single nucleotide polymorphisms |
title_full | MSProGene: integrative proteogenomics beyond six-frames and single nucleotide polymorphisms |
title_fullStr | MSProGene: integrative proteogenomics beyond six-frames and single nucleotide polymorphisms |
title_full_unstemmed | MSProGene: integrative proteogenomics beyond six-frames and single nucleotide polymorphisms |
title_short | MSProGene: integrative proteogenomics beyond six-frames and single nucleotide polymorphisms |
title_sort | msprogene: integrative proteogenomics beyond six-frames and single nucleotide polymorphisms |
topic | Ismb/Eccb 2015 Proceedings Papers Committee July 10 to July 14, 2015, Dublin, Ireland |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4765881/ https://www.ncbi.nlm.nih.gov/pubmed/26072472 http://dx.doi.org/10.1093/bioinformatics/btv236 |
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