Abstract

BackgroundThe development of next generation sequencing (NGS) methods led to a rapid rise in the generation of large genomic datasets, but the development of user-friendly tools to analyze and visualize these datasets has not developed at the same pace. This presents a two-fold challenge to biologists; the expertise to select an appropriate data analysis pipeline, and the need for bioinformatics or programming skills to apply this pipeline. The development of graphical user interface (GUI) applications hosted on web-based servers such as Shiny can make complex workflows accessible across operating systems and internet browsers to those without programming knowledge.ResultsWe have developed GENAVi (Gene Expression Normalization Analysis and Visualization) to provide a user-friendly interface for normalization and differential expression analysis (DEA) of human or mouse feature count level RNA-Seq data. GENAVi is a GUI based tool that combines Bioconductor packages in a format for scientists without bioinformatics expertise. We provide a panel of 20 cell lines commonly used for the study of breast and ovarian cancer within GENAVi as a foundation for users to bring their own data to the application. Users can visualize expression across samples, cluster samples based on gene expression or correlation, calculate and plot the results of principal components analysis, perform DEA and gene set enrichment and produce plots for each of these analyses. To allow scalability for large datasets we have provided local install via three methods. We improve on available tools by offering a range of normalization methods and a simple to use interface that provides clear and complete session reporting and for reproducible analysis.ConclusionThe development of tools using a GUI makes them practical and accessible to scientists without bioinformatics expertise, or access to a data analyst with relevant skills. While several GUI based tools are currently available for RNA-Seq analysis we improve on these existing tools. This user-friendly application provides a convenient platform for the normalization, analysis and visualization of gene expression data for scientists without bioinformatics expertise.

Highlights

  • The development of generation sequencing (NGS) methods led to a rapid rise in the generation of large genomic datasets, but the development of user-friendly tools to analyze and visualize these datasets has not developed at the same pace

  • The report provides the complete list of packages and their versions used within the session to perform the analysis, allowing users to maintain an easy to view and Results We have developed a user-friendly graphical user interface (GUI) based Shiny web application to host our own catalog of RNA-seq data and provide a platform for those without bioinformatics expertise to analyze their own data

  • We performed a search for open source RNA-Seq analysis tools that did not require any programming expertise to run, used stable and maintained established packages in R or Bioconductor and that operate through a GUI that are currently active

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Summary

Introduction

The development of generation sequencing (NGS) methods led to a rapid rise in the generation of large genomic datasets, but the development of user-friendly tools to analyze and visualize these datasets has not developed at the same pace This presents a two-fold challenge to biologists; the expertise to select an appropriate data analysis pipeline, and the need for bioinformatics or programming skills to apply this pipeline. The downstream analysis (normalization, differential expression and plotting the results of each) often requires several iterations and can be more efficiently performed by the researcher who designed the experiment, if they have the analytic expertise This scenario presents a twofold challenge to biologists; selection of the most appropriate data analysis pipeline, which often consists of multiple independent analytic packages [4], and the need for sufficient bioinformatics skills to apply this pipeline to their processed RNA-Seq data

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