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Updated: Dec 6, 2025

Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation
Published on: January 16, 2019
CUBAP: an interactive web portal for analyzing codon usage biases across populations
Matthew W Hodgman1, Justin B Miller1, Taylor E Meurs1
1Department of Biology, Brigham Young University, Provo, UT 84602, USA.
Population-specific codon usage biases impact gene expression and disease. Our web server, CUBAP, analyzes these differences, successfully predicting origins and revealing disease-associated genetic variations.
Area of Science:
- Genomics
- Molecular Biology
- Bioinformatics
Background:
- Synonymous codon usage influences gene expression, mRNA/protein structure, and disease.
- Population-specific codon usage biases are understudied.
- Understanding these biases is crucial for interpreting genetic variations.
Purpose of the Study:
- To develop a web server (CUBAP) for analyzing population-specific codon usage biases.
- To investigate differences in codon usage across diverse populations.
- To explore the implications of these biases for gene function and disease association.
Main Methods:
- Utilized the 1000 Genomes Project data for 17,634 genes.
- Calculated and visualized population-specific codon frequencies, codon aversion, codon pairing, ramp sequences, and nucleotide composition.
- Developed the CUBAP web server (https://cubap.byu.edu) for comprehensive analysis.
Main Results:
- Identified significant population-specific differences in codon pairing for 35.8% of genes.
- Achieved high accuracy (98.8% African, 100% East Asian) in predicting individuals' origins based on codon pairing.
- Discovered a decreased CTG pairing bias in the IRGM gene in East Asian and African populations, potentially affecting Crohn's disease association.
Conclusions:
- CUBAP provides a valuable tool for analyzing population-specific codon usage biases.
- Codon pairing variations can serve as markers for population origin.
- Synonymous codon usage differences have functional implications for gene expression and disease susceptibility across populations.
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