Bennett Mark, Evans Katie Ellen, Yu Shirong, Teng Yumin, Webster Richard M, Powell James, Waters Raymond, Reed Simon H
Cancer and Genetics Building, Cardiff University, School of Medicine, Heath Park, Cardiff, CF14 4XN, UK.
Sci Rep. 2015 Aug 26;5:13395. doi: 10.1038/srep13395.
ChIP-chip is a microarray based technology for determining the genomic locations of chromatin bound factors of interest, such as proteins. Standard ChIP-chip analyses employ peak detection methodologies to generate lists of genomic binding sites. No previously published method exists to enable comparative analyses of enrichment levels derived from datasets examining different experimental conditions. This restricts the use of the technology to binary comparisons of presence or absence of features between datasets. Here we present the R package Sandcastle — Software for the Analysis and Normalisation of Data from ChIP-chip AssayS of Two or more Linked Experiments — which allows for comparative analyses of data from multiple experiments by normalising all datasets to a common background. Relative changes in binding levels between experimental datasets can thus be determined, enabling the extraction of latent information from ChIP-chip experiments. Novel enrichment detection and peak calling algorithms are also presented, with a range of graphical tools, which facilitate these analyses. The software and documentation are available for download from http://reedlab.cardiff.ac.uk/sandcastle.
染色质免疫沉淀芯片(ChIP-chip)是一种基于微阵列的技术,用于确定感兴趣的染色质结合因子(如蛋白质)在基因组中的位置。标准的ChIP-chip分析采用峰值检测方法来生成基因组结合位点列表。目前还没有已发表的方法能够对来自不同实验条件数据集的富集水平进行比较分析。这将该技术的应用限制在数据集之间特征存在与否的二元比较上。在此,我们展示了R软件包Sandcastle——用于两个或多个相关实验的ChIP-chip分析数据的分析和归一化软件——它通过将所有数据集归一化到一个共同背景,允许对多个实验的数据进行比较分析。这样就可以确定实验数据集之间结合水平的相对变化,从而从ChIP-chip实验中提取潜在信息。还介绍了新的富集检测和峰值调用算法,以及一系列图形工具,以促进这些分析。该软件和文档可从http://reedlab.cardiff.ac.uk/sandcastle下载。