Whole Exome Sequencing/ analysis
Unlock the Genetic Code Behind Complex Traits and Diseases At AfroBiomics, our Whole Exome Sequencing (WES) service provides a cost-effective and highly informative approach to analyze all protein-coding regions (exons) of the genome. These exons represent just 1–2% of the human genome but harbor approximately 85% of disease-related variants, making WES a powerful tool for both research and clinical applications.
What We Offer: Comprehensive Exome Coverage: High-depth sequencing of all exons across the genome for accurate variant detection.
Variant Discovery & Annotation: Detection of single nucleotide variants (SNVs), insertions, deletions (INDELs), and rare mutations linked to genetic disorders.
Bioinformatics Analysis: From raw data QC and reference alignment to functional annotation and personalized interpretation.
Clinical & Research Utility: Ideal for investigating Mendelian diseases, cancer genomics, rare disorders, and candidate gene validation.
Key Features: Advanced library prep and capture technology
State-of-the-art high-throughput sequencing platforms
Customizable pipelines for population or individual-level studies
Integrative analysis with phenotypic or transcriptomic data (upon request)
Applications: Genetic diagnostics for rare inherited conditions
Cancer mutation profiling
Pharmacogenomics and personalized medicine
Population genetics and evolutionary studies
Why Choose AfroBiomics? Deep expertise in genomics and bioinformatics tailored for African populations
Robust quality control and validated analytical workflows
End-to-end support from study design to biological interpretation
Affordable, locally-delivered service with global quality standards
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