Texas:  11104 W Airport Blvd Ste. 121, Stafford, TX 77477
+1 (346) 635 8058
info@novagendx.com

Whole Genome Sequencing

One Breakthrough Test. Complete Genetic Insight. A Lifetime of Answers.

Discover the Full Story of Your DNA

Unlike standard genetic panels, WGS examines both coding (exons) and non-coding (introns) regions, giving clinicians access to vital information often missed by other tests. The result? Faster, clearer, and more confident diagnoses for patients across all stages of life. Whether you are searching for the cause of a medical condition or taking a proactive approach to your health, WGS offers unparalleled precision and long-term clinical value.

Why the Trio Approach Matters

Adding DNA samples from both biological parents—or other close relatives when necessary—allows our experts to interpret results with greater context and confidence. This family-based “trio” analysis helps differentiate inherited variants from new, spontaneous mutations, improving accuracy and speed in diagnosis.

  • Increases diagnostic yield by up to 15%
  • Reduces uncertain findings (VUS) to 18.9%, compared with 27.6% without trio data
  • Minimizes the need for additional testing and shortens the path to effective care

If parental samples cannot be obtained, our specialists can guide you on alternative relative sampling for best results.

Learn About Trio Testing Options

Explore Genome Testing Options at Novagen Clinical Lab

We offer cutting-edge genome tests designed to uncover complex genetic conditions, assess inherited risk, and guide clinical care.

GenSeq® – Comprehensive Whole Genome Sequencing

Gain a complete, detailed look at your genome, including both protein-coding and non-coding regions, for a thorough understanding of genetic influences on health.

What's Included:
  • Full nuclear genome analysis
  • Detection of repeat expansion disorders (e.g., DMPK, FMR1)
  • Mitochondrial genome sequencing and deletion screening
  • Complimentary reanalysis recommended after 18–24 months or following major health updates
Sample Requirements:
  • Proband: Blood (2–5 mL in EDTA, lavender top)
  • Parents/relatives: Blood (2–5 mL in EDTA) or Buccal swabs (2)
Test Codes:
  • Trio: J774a
  • Duo: J774e
  • Proband only: J774b
Turnaround Time:
  • Full report: 4 weeks
  • Mitochondrial genome report: 3–4 weeks

GenSeq Xpress® – Rapid Whole Genome Sequencing

For urgent cases requiring immediate answers, GenSeq Xpress® delivers rapid and accurate results without compromising depth or quality.

What's Included:
  • Complete genome analysis with provisional findings within one week
  • Detection of repeat expansion disorders
  • Mitochondrial genome sequencing and deletion screening
  • One-time complimentary reanalysis included
Sample Requirements:
  • Proband: Blood (2–5 mL in EDTA, lavender top)
  • Parents/relatives: Blood (2–5 mL in EDTA) or Buccal swabs (2)
Test Codes:
  • Trio: TH78a
  • Duo: TH78e
  • Proband only: TH78b
Turnaround Time:
  • Preliminary report: 5–7 days
  • Final report: 14 days
  • Mitochondrial genome report: 3–4 weeks

Note: Turnaround time begins when samples are received and processed in our lab. External delays may impact processing times.