FlexStat: Combinatory differentially expressed protein extraction

IF 2.4 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Senuri De Silva, Asfa Alli-Shaik, J. Gunaratne
{"title":"FlexStat: Combinatory differentially expressed protein extraction","authors":"Senuri De Silva, Asfa Alli-Shaik, J. Gunaratne","doi":"10.1093/bioadv/vbae056","DOIUrl":null,"url":null,"abstract":"\n \n \n Mass spectrometry-based system proteomics allows identification of dysregulated protein hubs and associated disease-related features. Obtaining differentially expressed proteins (DEPs) is the most important step of downstream bioinformatics analysis. However, the extraction of statistically significant DEPs from datasets with multiple experimental conditions or disease types through currently available tools remains a laborious task. More often such an analysis requires considerable bioinformatics expertise, making it inaccessible to researchers with limited computational analytics experience.\n \n \n \n To uncover the differences among the many conditions within the data in a user-friendly manner, here we introduce FlexStat, a web-based interface that extracts DEPs through combinatory analysis. This tool accepts a protein expression matrix as input and systematically generates DEP results for every conceivable combination of various experimental conditions or disease types. FlexStat includes a suite of robust statistical tools for data preprocessing, in addition to DEP extraction, and publication-ready visualization, which are built on established R scientific libraries in an automated manner. This analytics suite was validated in diverse public proteomic datasets to showcase its high performance of rapid and simultaneous pairwise comparisons of comprehensive data sets.\n \n \n \n FlexStat is implemented in R and is freely available at https://jglab.shinyapps.io/flexstatv1-pipeline-only/. The source code is accessible at https://github.com/kts-desilva/FlexStat/tree/main.\n \n \n \n Supplementary data are available at Bioinformatics Advances online.\n","PeriodicalId":72368,"journal":{"name":"Bioinformatics advances","volume":null,"pages":null},"PeriodicalIF":2.4000,"publicationDate":"2024-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioinformatics advances","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/bioadv/vbae056","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATHEMATICAL & COMPUTATIONAL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Mass spectrometry-based system proteomics allows identification of dysregulated protein hubs and associated disease-related features. Obtaining differentially expressed proteins (DEPs) is the most important step of downstream bioinformatics analysis. However, the extraction of statistically significant DEPs from datasets with multiple experimental conditions or disease types through currently available tools remains a laborious task. More often such an analysis requires considerable bioinformatics expertise, making it inaccessible to researchers with limited computational analytics experience. To uncover the differences among the many conditions within the data in a user-friendly manner, here we introduce FlexStat, a web-based interface that extracts DEPs through combinatory analysis. This tool accepts a protein expression matrix as input and systematically generates DEP results for every conceivable combination of various experimental conditions or disease types. FlexStat includes a suite of robust statistical tools for data preprocessing, in addition to DEP extraction, and publication-ready visualization, which are built on established R scientific libraries in an automated manner. This analytics suite was validated in diverse public proteomic datasets to showcase its high performance of rapid and simultaneous pairwise comparisons of comprehensive data sets. FlexStat is implemented in R and is freely available at https://jglab.shinyapps.io/flexstatv1-pipeline-only/. The source code is accessible at https://github.com/kts-desilva/FlexStat/tree/main. Supplementary data are available at Bioinformatics Advances online.
FlexStat:组合式差异表达蛋白质提取
基于质谱技术的系统蛋白质组学可以识别调控失调的蛋白质中心和相关的疾病特征。获取差异表达蛋白(DEPs)是下游生物信息学分析最重要的一步。然而,通过现有工具从具有多种实验条件或疾病类型的数据集中提取具有统计学意义的差异表达蛋白仍然是一项艰巨的任务。这种分析往往需要大量的生物信息学专业知识,这使得计算分析经验有限的研究人员无法胜任。 为了以用户友好的方式揭示数据中多种条件之间的差异,我们在此介绍 FlexStat,这是一种基于网络的界面,可通过组合分析提取 DEPs。该工具接受蛋白质表达矩阵作为输入,并为各种实验条件或疾病类型的每一种可想象的组合系统地生成 DEP 结果。FlexStat 包括一套强大的统计工具,用于数据预处理、DEP 提取和可发布的可视化,这些工具都是以自动化方式建立在成熟的 R 科学库上。该分析套件已在各种公共蛋白质组数据集中进行了验证,以展示其对综合数据集进行快速、同步配对比较的高性能。 FlexStat 使用 R 语言实现,可在 https://jglab.shinyapps.io/flexstatv1-pipeline-only/ 免费获取。源代码可从 https://github.com/kts-desilva/FlexStat/tree/main 获取。 补充数据可在 Bioinformatics Advances 在线查阅。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
1.60
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信