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Whole Exome Sequencing (WES)

Numeric Diagnostics provides next-generation sequencing (NGS) services using the AVITI System platform, delivering high-quality genomic data for comprehensive analysis.

Focus on What Matters Most in the Genome

Whole Exome Sequencing (WES) is a targeted genomic approach that focuses on sequencing the exome — the protein-coding regions of the genome, which account for approximately 1–2% of the genome but contain the majority of known disease-associated variants.

Using next-generation sequencing (NGS), exonic regions are selectively captured and sequenced, followed by bioinformatics analysis to identify variants such as single nucleotide variants (SNVs) and insertions or deletions (indels). By concentrating on regions most likely to impact protein function, WES offers a cost-effective and efficient method for genetic analysis.

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State-of-the-Art Technology

Industry-leading Sequencer

Our NGS services are powered by the AVITI System, delivering high-quality data with exceptional accuracy and efficiency. This advanced platform enables us to generate reliable genomic data across a wide range of applications, from whole genome to targeted sequencing.

Advantages

Targeted Efficiency

Focuses on coding regions where most known disease variants occur.

Cost-Effective

Lower sequencing cost compared to whole genome sequencing.

Reduced data size enables quicker turnaround times.

Faster Analysis
Clinical Relevancy

Ideal for identifying variants linked to genetic disorder.

More in our brochure

Find out more about our WES service.

Contact Us

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Reach out to discuss your whole genome sequencing needs today.