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Confidence: a web app for cross-platform differential gene expression analysis, gene scoring, and enrichment analysis
Abhishek Shastry1, Benjamin P Ott2, Tanvi Nandani2,3,4
1Department of Medicine, Queen's University, Kingston, K7L 3N6, Canada.
Scientific Reports
|April 27, 2026
Summary
Confidence is a new web tool for RNA-seq analysis, simplifying gene prioritization with a Confidence Score (CS). It addresses challenges in bioinformatics, offering intuitive gene selection for disease and treatment research.
Area of Science:
- Genomics
- Bioinformatics
- Computational Biology
Background:
- RNA sequencing (RNA-seq) is crucial for quantifying transcript abundance and identifying differential gene expression.
- Current RNA-seq analysis faces challenges including variability in results from different packages, complex bioinformatics requirements, and lack of intuitive gene prioritization methods.
Purpose of the Study:
- To develop a user-friendly, web-based application called Confidence for simultaneous statistical analysis of RNA-seq count data.
- To address the need for intuitive gene prioritization and overcome limitations of existing RNA-seq analytical packages.
Main Methods:
- Developed Confidence, a web application for RNA-seq data analysis.
- Incorporated a Confidence Score (CS) from 1 to 4 for gene prioritization, with 4 indicating high confidence.
- Integrated pathway analysis for biological context of prioritized genes.
Main Results:
- Confidence provides a rapid and intuitive 'wide-net' approach to RNA-seq analysis.
- The Confidence Score (CS) enables unbiased gene selection and identification of novel genes associated with disease/treatment models across species.
- The application facilitates the generation of publication-quality figures.
Conclusions:
- Confidence offers a novel strategy for target gene prioritization in RNA-seq analysis.
- The tool simplifies complex bioinformatics tasks, making advanced RNA-seq analysis more accessible.
- Confidence aids in identifying significant genes and placing them within relevant biological pathways for further investigation.
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