Cargando…

dCLIP: a computational approach for comparative CLIP-seq analyses

Although comparison of RNA-protein interaction profiles across different conditions has become increasingly important to understanding the function of RNA-binding proteins (RBPs), few computational approaches have been developed for quantitative comparison of CLIP-seq datasets. Here, we present an e...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Tao, Xie, Yang, Xiao, Guanghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4054096/
https://www.ncbi.nlm.nih.gov/pubmed/24398258
http://dx.doi.org/10.1186/gb-2014-15-1-r11
_version_ 1782320504726618112
author Wang, Tao
Xie, Yang
Xiao, Guanghua
author_facet Wang, Tao
Xie, Yang
Xiao, Guanghua
author_sort Wang, Tao
collection PubMed
description Although comparison of RNA-protein interaction profiles across different conditions has become increasingly important to understanding the function of RNA-binding proteins (RBPs), few computational approaches have been developed for quantitative comparison of CLIP-seq datasets. Here, we present an easy-to-use command line tool, dCLIP, for quantitative CLIP-seq comparative analysis. The two-stage method implemented in dCLIP, including a modified MA normalization method and a hidden Markov model, is shown to be able to effectively identify differential binding regions of RBPs in four CLIP-seq datasets, generated by HITS-CLIP, iCLIP and PAR-CLIP protocols. dCLIP is freely available at http://qbrc.swmed.edu/software/.
format Online
Article
Text
id pubmed-4054096
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-40540962014-06-12 dCLIP: a computational approach for comparative CLIP-seq analyses Wang, Tao Xie, Yang Xiao, Guanghua Genome Biol Software Although comparison of RNA-protein interaction profiles across different conditions has become increasingly important to understanding the function of RNA-binding proteins (RBPs), few computational approaches have been developed for quantitative comparison of CLIP-seq datasets. Here, we present an easy-to-use command line tool, dCLIP, for quantitative CLIP-seq comparative analysis. The two-stage method implemented in dCLIP, including a modified MA normalization method and a hidden Markov model, is shown to be able to effectively identify differential binding regions of RBPs in four CLIP-seq datasets, generated by HITS-CLIP, iCLIP and PAR-CLIP protocols. dCLIP is freely available at http://qbrc.swmed.edu/software/. BioMed Central 2014 2014-01-07 /pmc/articles/PMC4054096/ /pubmed/24398258 http://dx.doi.org/10.1186/gb-2014-15-1-r11 Text en Copyright © 2014 Wang 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
Wang, Tao
Xie, Yang
Xiao, Guanghua
dCLIP: a computational approach for comparative CLIP-seq analyses
title dCLIP: a computational approach for comparative CLIP-seq analyses
title_full dCLIP: a computational approach for comparative CLIP-seq analyses
title_fullStr dCLIP: a computational approach for comparative CLIP-seq analyses
title_full_unstemmed dCLIP: a computational approach for comparative CLIP-seq analyses
title_short dCLIP: a computational approach for comparative CLIP-seq analyses
title_sort dclip: a computational approach for comparative clip-seq analyses
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4054096/
https://www.ncbi.nlm.nih.gov/pubmed/24398258
http://dx.doi.org/10.1186/gb-2014-15-1-r11
work_keys_str_mv AT wangtao dclipacomputationalapproachforcomparativeclipseqanalyses
AT xieyang dclipacomputationalapproachforcomparativeclipseqanalyses
AT xiaoguanghua dclipacomputationalapproachforcomparativeclipseqanalyses