Whole Genome Sequencing

One Powerful Test. Total Genetic Clarity. Lifelong Impact.

Why Choose Whole Genome Sequencing?

Unlike traditional methods, WGS looks at every part of your DNA, including both coding (exons) and non-coding (introns) regions. This means faster answers, fewer inconclusive results, and a better chance of uncovering the root cause of medical conditions. Whether you're seeking a diagnosis or planning ahead, WGS provides unmatched depth and precision.

The Power of Trio Testing

Including DNA from both biological parents—or close relatives if needed—enhances interpretation and increases diagnostic confidence. This “trio” approach allows our team to distinguish between inherited and spontaneous mutations with greater accuracy.

  • Increases diagnostic yield by up to 15%
  • Lowers uncertain findings (VUS) to 18.9% compared to 27.6% without trio data
  • Reduces unnecessary follow-up tests and accelerates care decisions

If parental samples aren’t available, we can advise on alternative family member options.

Learn About Trio Testing Options

Explore Genome Testing Options at Precise Clinical Lab Care

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

GenSeq® – Complete Whole Genome Sequencing

Get a full picture of your genome, including both protein-coding and non-coding regions, for deep diagnostic insight.

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

GenSeq Xpress® – Rapid Genome Sequencing

Ideal for time-sensitive or critical situations, GenSeq Xpress® delivers fast answers without compromising quality.

What's Included:
  • Full genome analysis with provisional results in under a week
  • Detects repeat expansion disorders
  • Includes mitochondrial genome and deletion screening
  • One-time free reanalysis included
Sample Requirements:
  • Proband: Blood (2–5mL in EDTA, lavender top)
  • Parents/Relatives: Blood (2–5mL in EDTA) or Buccal swabs (2)
Test Codes:
  • Trio: TH78a
  • Duo: TH78e
  • Proband only: TH78b
Turnaround Time:
  • Provisional findings in 5–7 days
  • Final report in 14 days
  • Mitochondrial genome report in 3–4 weeks

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