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.
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
Reach out to discuss your whole genome sequencing needs today.
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ADDRESS
1st Floor, Wisma Academy, 4A, Jalan 19/1, Seksyen 19, 46300 Petaling Jaya, Selangor
CONTACT US
+60 3-7497 2391
info@numericdx.com
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