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Oasis 2: improved online analysis of small RNA-seq data

BACKGROUND: Small RNA molecules play important roles in many biological processes and their dysregulation or dysfunction can cause disease. The current method of choice for genome-wide sRNA expression profiling is deep sequencing. RESULTS: Here we present Oasis 2, which is a new main release of the...

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Autores principales: Rahman, Raza-Ur, Gautam, Abhivyakti, Bethune, Jörn, Sattar, Abdul, Fiosins, Maksims, Magruder, Daniel Sumner, Capece, Vincenzo, Shomroni, Orr, Bonn, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5813365/
https://www.ncbi.nlm.nih.gov/pubmed/29444641
http://dx.doi.org/10.1186/s12859-018-2047-z
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author Rahman, Raza-Ur
Gautam, Abhivyakti
Bethune, Jörn
Sattar, Abdul
Fiosins, Maksims
Magruder, Daniel Sumner
Capece, Vincenzo
Shomroni, Orr
Bonn, Stefan
author_facet Rahman, Raza-Ur
Gautam, Abhivyakti
Bethune, Jörn
Sattar, Abdul
Fiosins, Maksims
Magruder, Daniel Sumner
Capece, Vincenzo
Shomroni, Orr
Bonn, Stefan
author_sort Rahman, Raza-Ur
collection PubMed
description BACKGROUND: Small RNA molecules play important roles in many biological processes and their dysregulation or dysfunction can cause disease. The current method of choice for genome-wide sRNA expression profiling is deep sequencing. RESULTS: Here we present Oasis 2, which is a new main release of the Oasis web application for the detection, differential expression, and classification of small RNAs in deep sequencing data. Compared to its predecessor Oasis, Oasis 2 features a novel and speed-optimized sRNA detection module that supports the identification of small RNAs in any organism with higher accuracy. Next to the improved detection of small RNAs in a target organism, the software now also recognizes potential cross-species miRNAs and viral and bacterial sRNAs in infected samples. In addition, novel miRNAs can now be queried and visualized interactively, providing essential information for over 700 high-quality miRNA predictions across 14 organisms. Robust biomarker signatures can now be obtained using the novel enhanced classification module. CONCLUSIONS: Oasis 2 enables biologists and medical researchers to rapidly analyze and query small RNA deep sequencing data with improved precision, recall, and speed, in an interactive and user-friendly environment. AVAILABILITY AND IMPLEMENTATION: Oasis 2 is implemented in Java, J2EE, mysql, Python, R, PHP and JavaScript. It is freely available at https://oasis.dzne.de ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2047-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-58133652018-02-16 Oasis 2: improved online analysis of small RNA-seq data Rahman, Raza-Ur Gautam, Abhivyakti Bethune, Jörn Sattar, Abdul Fiosins, Maksims Magruder, Daniel Sumner Capece, Vincenzo Shomroni, Orr Bonn, Stefan BMC Bioinformatics Software BACKGROUND: Small RNA molecules play important roles in many biological processes and their dysregulation or dysfunction can cause disease. The current method of choice for genome-wide sRNA expression profiling is deep sequencing. RESULTS: Here we present Oasis 2, which is a new main release of the Oasis web application for the detection, differential expression, and classification of small RNAs in deep sequencing data. Compared to its predecessor Oasis, Oasis 2 features a novel and speed-optimized sRNA detection module that supports the identification of small RNAs in any organism with higher accuracy. Next to the improved detection of small RNAs in a target organism, the software now also recognizes potential cross-species miRNAs and viral and bacterial sRNAs in infected samples. In addition, novel miRNAs can now be queried and visualized interactively, providing essential information for over 700 high-quality miRNA predictions across 14 organisms. Robust biomarker signatures can now be obtained using the novel enhanced classification module. CONCLUSIONS: Oasis 2 enables biologists and medical researchers to rapidly analyze and query small RNA deep sequencing data with improved precision, recall, and speed, in an interactive and user-friendly environment. AVAILABILITY AND IMPLEMENTATION: Oasis 2 is implemented in Java, J2EE, mysql, Python, R, PHP and JavaScript. It is freely available at https://oasis.dzne.de ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2047-z) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-14 /pmc/articles/PMC5813365/ /pubmed/29444641 http://dx.doi.org/10.1186/s12859-018-2047-z Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Software
Rahman, Raza-Ur
Gautam, Abhivyakti
Bethune, Jörn
Sattar, Abdul
Fiosins, Maksims
Magruder, Daniel Sumner
Capece, Vincenzo
Shomroni, Orr
Bonn, Stefan
Oasis 2: improved online analysis of small RNA-seq data
title Oasis 2: improved online analysis of small RNA-seq data
title_full Oasis 2: improved online analysis of small RNA-seq data
title_fullStr Oasis 2: improved online analysis of small RNA-seq data
title_full_unstemmed Oasis 2: improved online analysis of small RNA-seq data
title_short Oasis 2: improved online analysis of small RNA-seq data
title_sort oasis 2: improved online analysis of small rna-seq data
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5813365/
https://www.ncbi.nlm.nih.gov/pubmed/29444641
http://dx.doi.org/10.1186/s12859-018-2047-z
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