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A ChIP-Seq Data Analysis Pipeline Based on Bioconductor Packages

Nowadays, huge volumes of chromatin immunoprecipitation-sequencing (ChIP-Seq) data are generated to increase the knowledge on DNA-protein interactions in the cell, and accordingly, many tools have been developed for ChIP-Seq analysis. Here, we provide an example of a streamlined workflow for ChIP-Se...

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Detalles Bibliográficos
Autores principales: Park, Seung-Jin, Kim, Jong-Hwan, Yoon, Byung-Ha, Kim, Seon-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korea Genome Organization 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389943/
https://www.ncbi.nlm.nih.gov/pubmed/28416945
http://dx.doi.org/10.5808/GI.2017.15.1.11
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author Park, Seung-Jin
Kim, Jong-Hwan
Yoon, Byung-Ha
Kim, Seon-Young
author_facet Park, Seung-Jin
Kim, Jong-Hwan
Yoon, Byung-Ha
Kim, Seon-Young
author_sort Park, Seung-Jin
collection PubMed
description Nowadays, huge volumes of chromatin immunoprecipitation-sequencing (ChIP-Seq) data are generated to increase the knowledge on DNA-protein interactions in the cell, and accordingly, many tools have been developed for ChIP-Seq analysis. Here, we provide an example of a streamlined workflow for ChIP-Seq data analysis composed of only four packages in Bioconductor: dada2, QuasR, mosaics, and ChIPseeker. ‘dada2’ performs trimming of the high-throughput sequencing data. ‘QuasR’ and ‘mosaics’ perform quality control and mapping of the input reads to the reference genome and peak calling, respectively. Finally, ‘ChIPseeker’ performs annotation and visualization of the called peaks. This workflow runs well independently of operating systems (e.g., Windows, Mac, or Linux) and processes the input fastq files into various results in one run. R code is available at github: https://github.com/ddhb/Workflow_of_Chipseq.git.
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spelling pubmed-53899432017-04-17 A ChIP-Seq Data Analysis Pipeline Based on Bioconductor Packages Park, Seung-Jin Kim, Jong-Hwan Yoon, Byung-Ha Kim, Seon-Young Genomics Inform Original Article Nowadays, huge volumes of chromatin immunoprecipitation-sequencing (ChIP-Seq) data are generated to increase the knowledge on DNA-protein interactions in the cell, and accordingly, many tools have been developed for ChIP-Seq analysis. Here, we provide an example of a streamlined workflow for ChIP-Seq data analysis composed of only four packages in Bioconductor: dada2, QuasR, mosaics, and ChIPseeker. ‘dada2’ performs trimming of the high-throughput sequencing data. ‘QuasR’ and ‘mosaics’ perform quality control and mapping of the input reads to the reference genome and peak calling, respectively. Finally, ‘ChIPseeker’ performs annotation and visualization of the called peaks. This workflow runs well independently of operating systems (e.g., Windows, Mac, or Linux) and processes the input fastq files into various results in one run. R code is available at github: https://github.com/ddhb/Workflow_of_Chipseq.git. Korea Genome Organization 2017-03 2017-03-29 /pmc/articles/PMC5389943/ /pubmed/28416945 http://dx.doi.org/10.5808/GI.2017.15.1.11 Text en Copyright © 2017 by the Korea Genome Organization http://creativecommons.org/licenses/by-nc/4.0/ It is identical to the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/).
spellingShingle Original Article
Park, Seung-Jin
Kim, Jong-Hwan
Yoon, Byung-Ha
Kim, Seon-Young
A ChIP-Seq Data Analysis Pipeline Based on Bioconductor Packages
title A ChIP-Seq Data Analysis Pipeline Based on Bioconductor Packages
title_full A ChIP-Seq Data Analysis Pipeline Based on Bioconductor Packages
title_fullStr A ChIP-Seq Data Analysis Pipeline Based on Bioconductor Packages
title_full_unstemmed A ChIP-Seq Data Analysis Pipeline Based on Bioconductor Packages
title_short A ChIP-Seq Data Analysis Pipeline Based on Bioconductor Packages
title_sort chip-seq data analysis pipeline based on bioconductor packages
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389943/
https://www.ncbi.nlm.nih.gov/pubmed/28416945
http://dx.doi.org/10.5808/GI.2017.15.1.11
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