Whole Exome Sequencing
See What’s Hidden. Sequence What Matters.
Whole Exome Sequencing
Whole Exome Sequencing (WES) provides a deep dive into your protein-coding DNA regions to uncover the genetic roots of rare or unexplained health conditions. By sequencing over 22,000 genes, it helps identify inherited disorders, supports clinical diagnosis, and informs targeted treatment strategies when conventional tests fall short.
What Does It Do?
Whole Exome Sequencing (WES) examines all protein-coding regions of the genome to detect rare or complex disorders. It provides deep insights into genetic causes of unexplained health conditions.
Polygenic Risk Score (PRS)
Polygenic Risk Score is not typically used in WES but variant classification is based on ACMG/AMP guidelines to interpret risk or pathogenicity.
Who Benefits?
Individuals with undiagnosed or rare genetic disorders.
Families with multiple members affected by complex conditions.
Patients seeking advanced genomic diagnostics.
Core Pillars
Explore the Exome
Analyze critical regions affecting health.
Explain the Unexplained
Identify causes of rare diseases.
Enable Informed Choices
Guide future treatments and testing.
Free Consultation
Speak with our genetic counselors
Technical Specifications
| Specification | Value |
|---|---|
| Technique | Next-Generation Sequencing (NGS) |
| Platform | Illumina NovaSeq/NextSeq |
| Bioinformatic Tools | BWA, GATK, Annovar |
| Coverage | 22,000 genes (coding regions) |
| Accuracy | 99% in targeted regions |
| Sample Type | Blood or Saliva |
| Turnaround Time | 3–4 weeks |
Ready to Unlock Your Genetic Insights?
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