Advanced Genomic Testing
Whole Genome Sequencing
The most comprehensive genetic test available — analyzing all 6 billion base pairs of your DNA in a single study.
What Is Whole Genome Sequencing?
Whole Genome Sequencing (WGS) reads every letter of your DNA code — all 3 billion base pairs inherited from each parent. Unlike targeted panels that examine only known disease-associated genes, WGS captures the entire genome, including coding regions, regulatory sequences, and structural variants that panel tests routinely miss.
At Genetic Insights, the clinical relevance of WGS is determined by Dr. Vaughn; translating raw genomic data into actionable medical guidance for you and your PCP.
Why Choose Whole Genome Sequencing?
Complete Coverage
Examines all genes simultaneously — no need to guess which panel to order first.
Detects Rare Variants
Identifies pathogenic variants in genes not included on standard disease panels.
Structural Variant Detection
Finds large deletions, duplications, and inversions that SNP arrays and limited panels miss.
Future-Proof Data
Your genome can be re-analyzed again and again through out your life as new disease-gene associations are discovered — without the need for re-testing.
Pharmacogenomics Included
98% of people carry genetic variants that affect the metabolism of many commonly used medications. How these enzymes effect blood levels of these drugs can be a crucial determinant of treatment sucess
One Test, Great Lifelong Value
In 2016 Illumina’s “Understand Your Genome” Program" , charged $2,900 for full genome sequencing with medical variant analysis. Today, WGS can be done for $400.
Clinical Reference
The Application of WGS to Genetic Risk Screening
A detailed overview of how whole genome sequencing is applied in clinical practice for comprehensive genetic risk assessment.
Download PDFHow It Works
Consultation
Meet with Dr. Vaughn to review your personal and family history and confirm that WGS is the right study for your goals.
Sample Collection
A simple cheek swab collected at home is all that is needed
Laboratory Analysis
Your sample is processed using high-depth sequencing (30× coverage or greater).
Expert Interpretation
Dr. Vaughn reviews the full variant report, cross-referencing your clinical history to distinguish meaningful findings from benign variants.
Results & Action Plan
You receive a plain-language summary and a structured report your primary care physician can act on immediately.
Common Questions
Ready to Learn What Your Genome Can Tell You?
Schedule a consultation with Dr. Vaughn to find out whether Whole Genome Sequencing is right for you.