Whole Genome Sequencing
Whole Genome Sequencing (WGS) is the most comprehensive genetic test available — analyzing 98% of the entire human genome including all protein-coding genes, non-coding regions, regulatory sequences, and structural variants. While WES covers only 1–2% of the genome, WGS captures everything, making it the gold standard for diagnosing complex rare diseases, ending diagnostic odysseys, guiding precision medicine, and uncovering genetic predispositions across all known conditions. This is the test for when every other test has failed to provide answers.
Complete genome analysis
98% of the entire genome — coding and non-coding regions, regulatory sequences, all 23 chromosome pairs
Non-coding region variants
Regulatory, intronic, and intergenic variants invisible to WES — critical for conditions WES cannot diagnose
Structural variants (SVs)
Large insertions, deletions, inversions, and translocations at base-pair resolution
De novo mutations
New spontaneous mutations not inherited from parents — essential for rare disease diagnosis in children
Precision medicine
Identify DNA changes that align medications with your genetic profile — for cancer, diabetes, heart disease
Disease prevention
Genetic predispositions encoded across the entire genome — build a strategic prevention plan from your DNA
Pre-test counseling (recommended)
Speak with our Genomic Expert to confirm WGS is appropriate for your clinical situation and discuss what findings — including incidental findings — may mean.
Order with referral confirmation
Confirm doctor's referral. Your home collection kit ships within 24 hours — EDTA blood tube and saliva swab included.
Blood + Saliva sample collection
3–4ml EDTA blood + saliva swab at home. Return using the prepaid courier label included in your kit.
Whole genome NGS sequencing
Your entire genome is sequenced at 30X depth on Illumina platform — covering 95–98% of all base pairs in our NABL & CAP accredited lab.
Bioinformatics analysis
Advanced pipeline analyzes SNVs, CNVs, SVs, and non-coding variants. ACMG guidelines applied for variant classification. Primary, incidental, and carrier findings all reported.
Comprehensive report + Genomic Expert consultation
Detailed WGS report in 56 days (8 weeks). Deep-dive consultation with our Genomic Expert to review all findings and coordinate specialist care as needed.
Your Whole Genome Sequencing Report
A snapshot of your comprehensive WGS clinical report
- 95–98% of entire genome sequenced
- 30X coverage depth — high accuracy
- Coding + non-coding + regulatory regions
- SNV + CNV + Structural variant analysis
- NABL & CAP accredited lab
- Post-result Genomic Expert consultation