SVAw - a web-based application tool for automated surrogate variable analysis of gene expression studies.

Q2 Decision Sciences
Mehdi Pirooznia, Fayaz Seifuddin, Fernando S Goes, Jeffrey T Leek, Peter P Zandi
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引用次数: 0

Abstract

Background: Surrogate variable analysis (SVA) is a powerful method to identify, estimate, and utilize the components of gene expression heterogeneity due to unknown and/or unmeasured technical, genetic, environmental, or demographic factors. These sources of heterogeneity are common in gene expression studies, and failing to incorporate them into the analysis can obscure results. Using SVA increases the biological accuracy and reproducibility of gene expression studies by identifying these sources of heterogeneity and correctly accounting for them in the analysis.

Results: Here we have developed a web application called SVAw (Surrogate variable analysis Web app) that provides a user friendly interface for SVA analyses of genome-wide expression studies. The software has been developed based on open source bioconductor SVA package. In our software, we have extended the SVA program functionality in three aspects: (i) the SVAw performs a fully automated and user friendly analysis workflow; (ii) It calculates probe/gene Statistics for both pre and post SVA analysis and provides a table of results for the regression of gene expression on the primary variable of interest before and after correcting for surrogate variables; and (iii) it generates a comprehensive report file, including graphical comparison of the outcome for the user.

Conclusions: SVAw is a web server freely accessible solution for the surrogate variant analysis of high-throughput datasets and facilitates removing all unwanted and unknown sources of variation. It is freely available for use at http://psychiatry.igm.jhmi.edu/sva. The executable packages for both web and standalone application and the instruction for installation can be downloaded from our web site.

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SVAw - 一种基于网络的应用工具,用于对基因表达研究进行自动代理变量分析。
背景:替代变量分析(SVA)是一种功能强大的方法,可用于识别、估计和利用因未知和/或未测量的技术、遗传、环境或人口因素而导致的基因表达异质性成分。这些异质性来源在基因表达研究中很常见,如果不将其纳入分析,就会使结果模糊不清。使用 SVA 可以识别这些异质性来源,并在分析中正确考虑它们,从而提高基因表达研究的生物学准确性和可重复性:在此,我们开发了一款名为 SVAw(代理变量分析网络应用程序)的网络应用程序,它为全基因组表达研究的 SVA 分析提供了友好的用户界面。该软件是基于开源生物诱导 SVA 软件包开发的。在我们的软件中,我们从三个方面扩展了 SVA 程序的功能:(i) SVAw 执行全自动且用户友好的分析工作流程;(ii) 计算 SVA 分析前和分析后的探针/基因统计量,并提供在校正替代变量前后基因表达对主要相关变量的回归结果表;(iii) 生成综合报告文件,包括为用户提供结果的图形比较:SVAw 是一种可免费访问的网络服务器解决方案,用于对高通量数据集进行代用变异分析,并有助于去除所有不需要的未知变异源。它可在 http://psychiatry.igm.jhmi.edu/sva 免费使用。网络和独立应用程序的可执行程序包以及安装说明可从我们的网站下载。
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来源期刊
Source Code for Biology and Medicine
Source Code for Biology and Medicine Decision Sciences-Information Systems and Management
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期刊介绍: Source Code for Biology and Medicine is a peer-reviewed open access, online journal that publishes articles on source code employed over a wide range of applications in biology and medicine. The journal"s aim is to publish source code for distribution and use in the public domain in order to advance biological and medical research. Through this dissemination, it may be possible to shorten the time required for solving certain computational problems for which there is limited source code availability or resources.
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