xIP-seq Platform: An Integrative Framework for High-Throughput Sequencing Data Analysis

Xin Wang, Mingxiang Teng, Guohua Wang, Yuming Zhao, Xu Han, Weixing Feng, Lang Li, J. Sanford, Yunlong Liu
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引用次数: 2

Abstract

We report an integrative bioinformatic platform for next-generation sequencing data analysis, xIP-seq, which is built on GenePattern package. The purpose for this tool is to provide analysis pipelines for data derived from next-generation sequencing following a variety of experiments using immunoprecipitation, such as ChIP-seq (chromatin immunoprecipitation following sequencing) for analysis of DNA binding protein, CLIP-seq (cross-linking immunoprecipitation following sequencing) for analysis of RNA binding protein, and MeDIP-seq (methylation DNA immunoprecipitation following sequencing) for DNA methylation profiles. xIP-seq platform provides standardized data pre-processing workflows which prepare raw data from various sequencing platforms for further analysis, and several bioinformatic applications including sequence annotation and analysis of Pol II binding pattern and histone modification.. The tertiary module for sequence annotation is particularly discussed. xIP-seq also allows users to construct new analysis pipelines tailored for individual biological interests by employing currently available modules or creating new ones. As an example, a “CLIP-seq Mapper” pipeline is created to map CLIP-seq-derived data to human genome to identify the genome-wide annotation of SFRS1 binding pattern. This implementation demonstrates the significance of xIP-seq platform to analyze massive amounts of next-generation sequencing data and provide automatic, flexible, and intelligent enterprise-level bioinformatic solutions.
xIP-seq平台:高通量测序数据分析的综合框架
我们报告了一个用于下一代测序数据分析的综合生物信息学平台,xIP-seq,它是建立在geneppattern包上的。该工具的目的是为使用免疫沉淀的各种实验后的下一代测序数据提供分析管道,例如用于分析DNA结合蛋白的ChIP-seq(测序后的染色质免疫沉淀),用于分析RNA结合蛋白的CLIP-seq(测序后的交联免疫沉淀)和用于分析DNA甲基化谱的MeDIP-seq(测序后的甲基化DNA免疫沉淀)。xIP-seq平台提供标准化的数据预处理工作流程,为进一步分析准备来自各种测序平台的原始数据,以及几种生物信息学应用,包括序列注释和Pol II结合模式分析和组蛋白修饰。重点讨论了序列标注的三级模块。xIP-seq还允许用户通过使用当前可用的模块或创建新的模块来构建针对个人生物学兴趣的新的分析管道。例如,建立了“CLIP-seq Mapper”管道,将CLIP-seq衍生的数据映射到人类基因组,以鉴定SFRS1结合模式的全基因组注释。这一实现证明了xIP-seq平台在分析海量下一代测序数据和提供自动化、灵活、智能的企业级生物信息学解决方案方面的重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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