Tyagi Punit, Bhide Mangesh
Laboratory of Biomedical Microbiology and Immunology, University of Veterinary Medicine and Pharmacy in Kosice, Kosice, Slovakia.
Department of Animal and Food Science, The Autonomous University of Barcelona, Barcelona, Spain.
PeerJ. 2021 Nov 9;9:e12415. doi: 10.7717/peerj.12415. eCollection 2021.
In the past decade, RNA sequencing and mass spectrometry based quantitative approaches are being used commonly to identify the differentially expressed biomarkers in different biological conditions. Data generated from these approaches come in different sizes (, count matrix, normalized list of differentially expressed biomarkers, etc.) and shapes (, sequences, spectral data, etc.). The list of differentially expressed biomarkers is used for functional interpretation and retrieve biological meaning, however, it requires moderate computational skills. Thus, researchers with no programming expertise find difficulty in data interpretation. Several bioinformatics tools are available to analyze such data; however, they are less flexible for performing the multiple steps of visualization and functional interpretation.
We developed an easy-to-use Shiny based web application (named as OMnalysis) that provides users with a single platform to analyze and visualize the differentially expressed data. The OMnalysis accepts the data in tabular form from edgeR, DESeq2, MaxQuant Perseus, R packages, and other similar software, which typically contains the list of differentially expressed genes or proteins, log of the fold change, log of the count per million, the value, -value, etc. The key features of the OMnalysis are multiple image type visualization and their dimension customization options, seven multiple hypothesis testing correction methods to get more significant gene ontology, network topology-based pathway analysis, and multiple databases support (KEGG, Reactome, PANTHER, biocarta, NCI-Nature Pathway Interaction Database PharmGKB and STRINGdb) for extensive pathway enrichment analysis. OMnalysis also fetches the literature information from PubMed to provide supportive evidence to the biomarkers identified in the analysis. In a nutshell, we present the OMnalysis as a well-organized user interface, supported by peer-reviewed R packages with updated databases for quick interpretation of the differential transcriptomics and proteomics data to biological meaning.
The OMnalysis codes are entirely written in R language and freely available at https://github.com/Punit201016/OMnalysis. OMnalysis can also be accessed from - http://lbmi.uvlf.sk/omnalysis.html. OMnalysis is hosted on a Shiny server at https://omnalysis.shinyapps.io/OMnalysis/. The minimum system requirements are: 4 gigabytes of RAM, i3 processor (or equivalent). It is compatible with any operating system (windows, Linux or Mac). The OMnalysis is heavily tested on Chrome web browsers; thus, Chrome is the preferred browser. OMnalysis works on Firefox and Safari.
在过去十年中,基于RNA测序和质谱的定量方法被广泛用于识别不同生物学条件下差异表达的生物标志物。这些方法产生的数据具有不同的大小(如计数矩阵、差异表达生物标志物的标准化列表等)和形式(如序列、光谱数据等)。差异表达生物标志物列表用于功能解释和获取生物学意义,然而,这需要一定的计算技能。因此,没有编程专业知识的研究人员在数据解释方面存在困难。有几种生物信息学工具可用于分析此类数据;然而,它们在执行可视化和功能解释的多个步骤时灵活性较差。
我们开发了一个基于Shiny的易于使用的网络应用程序(名为OMnalysis),为用户提供一个分析和可视化差异表达数据的单一平台。OMnalysis接受来自edgeR、DESeq2、MaxQuant Perseus、R包和其他类似软件的表格形式的数据,这些数据通常包含差异表达基因或蛋白质的列表、倍数变化的对数、每百万计数的对数、p值、q值等。OMnalysis的关键特性包括多种图像类型可视化及其维度定制选项、七种多重假设检验校正方法以获得更显著的基因本体、基于网络拓扑的通路分析以及多个数据库支持(KEGG、Reactome、PANTHER、biocarta、NCI-Nature Pathway Interaction Database、PharmGKB和STRINGdb)以进行广泛的通路富集分析。OMnalysis还从PubMed获取文献信息,为分析中鉴定的生物标志物提供支持性证据。简而言之,我们将OMnalysis展示为一个组织良好的用户界面,由经过同行评审的R包和更新的数据库支持,用于将差异转录组学和蛋白质组学数据快速解释为生物学意义。