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SPAR: small RNA-seq portal for analysis of sequencing experiments

The introduction of new high-throughput small RNA sequencing protocols that generate large-scale genomics datasets along with increasing evidence of the significant regulatory roles of small non-coding RNAs (sncRNAs) have highlighted the urgent need for tools to analyze and interpret large amounts o...

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Autores principales: Kuksa, Pavel P, Amlie-Wolf, Alexandre, Katanić, Živadin, Valladares, Otto, Wang, Li-San, Leung, Yuk Yee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030839/
https://www.ncbi.nlm.nih.gov/pubmed/29733404
http://dx.doi.org/10.1093/nar/gky330
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author Kuksa, Pavel P
Amlie-Wolf, Alexandre
Katanić, Živadin
Valladares, Otto
Wang, Li-San
Leung, Yuk Yee
author_facet Kuksa, Pavel P
Amlie-Wolf, Alexandre
Katanić, Živadin
Valladares, Otto
Wang, Li-San
Leung, Yuk Yee
author_sort Kuksa, Pavel P
collection PubMed
description The introduction of new high-throughput small RNA sequencing protocols that generate large-scale genomics datasets along with increasing evidence of the significant regulatory roles of small non-coding RNAs (sncRNAs) have highlighted the urgent need for tools to analyze and interpret large amounts of small RNA sequencing data. However, it remains challenging to systematically and comprehensively discover and characterize sncRNA genes and specifically-processed sncRNA products from these datasets. To fill this gap, we present Small RNA-seq Portal for Analysis of sequencing expeRiments (SPAR), a user-friendly web server for interactive processing, analysis, annotation and visualization of small RNA sequencing data. SPAR supports sequencing data generated from various experimental protocols, including smRNA-seq, short total RNA sequencing, microRNA-seq, and single-cell small RNA-seq. Additionally, SPAR includes publicly available reference sncRNA datasets from our DASHR database and from ENCODE across 185 human tissues and cell types to produce highly informative small RNA annotations across all major small RNA types and other features such as co-localization with various genomic features, precursor transcript cleavage patterns, and conservation. SPAR allows the user to compare the input experiment against reference ENCODE/DASHR datasets. SPAR currently supports analyses of human (hg19, hg38) and mouse (mm10) sequencing data. SPAR is freely available at https://www.lisanwanglab.org/SPAR.
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spelling pubmed-60308392018-07-10 SPAR: small RNA-seq portal for analysis of sequencing experiments Kuksa, Pavel P Amlie-Wolf, Alexandre Katanić, Živadin Valladares, Otto Wang, Li-San Leung, Yuk Yee Nucleic Acids Res Web Server Issue The introduction of new high-throughput small RNA sequencing protocols that generate large-scale genomics datasets along with increasing evidence of the significant regulatory roles of small non-coding RNAs (sncRNAs) have highlighted the urgent need for tools to analyze and interpret large amounts of small RNA sequencing data. However, it remains challenging to systematically and comprehensively discover and characterize sncRNA genes and specifically-processed sncRNA products from these datasets. To fill this gap, we present Small RNA-seq Portal for Analysis of sequencing expeRiments (SPAR), a user-friendly web server for interactive processing, analysis, annotation and visualization of small RNA sequencing data. SPAR supports sequencing data generated from various experimental protocols, including smRNA-seq, short total RNA sequencing, microRNA-seq, and single-cell small RNA-seq. Additionally, SPAR includes publicly available reference sncRNA datasets from our DASHR database and from ENCODE across 185 human tissues and cell types to produce highly informative small RNA annotations across all major small RNA types and other features such as co-localization with various genomic features, precursor transcript cleavage patterns, and conservation. SPAR allows the user to compare the input experiment against reference ENCODE/DASHR datasets. SPAR currently supports analyses of human (hg19, hg38) and mouse (mm10) sequencing data. SPAR is freely available at https://www.lisanwanglab.org/SPAR. Oxford University Press 2018-07-02 2018-05-04 /pmc/articles/PMC6030839/ /pubmed/29733404 http://dx.doi.org/10.1093/nar/gky330 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 Web Server Issue
Kuksa, Pavel P
Amlie-Wolf, Alexandre
Katanić, Živadin
Valladares, Otto
Wang, Li-San
Leung, Yuk Yee
SPAR: small RNA-seq portal for analysis of sequencing experiments
title SPAR: small RNA-seq portal for analysis of sequencing experiments
title_full SPAR: small RNA-seq portal for analysis of sequencing experiments
title_fullStr SPAR: small RNA-seq portal for analysis of sequencing experiments
title_full_unstemmed SPAR: small RNA-seq portal for analysis of sequencing experiments
title_short SPAR: small RNA-seq portal for analysis of sequencing experiments
title_sort spar: small rna-seq portal for analysis of sequencing experiments
topic Web Server Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030839/
https://www.ncbi.nlm.nih.gov/pubmed/29733404
http://dx.doi.org/10.1093/nar/gky330
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