Germline DNA
What you inherited
For hereditary risk, rare-disease investigation, carrier status, and proactive genomic screening.
Saliva or bloodWES and WGS
Next-generation clinical genomics
The right test for a specific clinical question
We sequence thousands of genes—or your entire genome—to support diagnosis, assess hereditary risk, and inform precision cancer care.
5specialized tests
25business days*
1report category included
*From the date the laboratory receives a valid sample.
A different question
Beyond nutrition and medication
Nutrigenetics and pharmacogenetics explain how your body responds to food and medicines. Clinical sequencing looks for inherited or tumor variants that matter for diagnosis and treatment.
Two families, two kinds of decisions
Somatic DNA or RNA
What is happening in the tumor
To identify changes that can help an oncology team select treatment or monitor disease.
Tumor tissue, blood, or RNASolid tumor, liquid biopsy, and RNA fusions
Interactive guide
What do you need to investigate?
Choose the closest scenario. We will show the test that usually answers that question best.
My main goal is to…
Clear comparison
Five tests, one view
Select a card to understand its scope, sample, and recommended use.
Inherited
Whole Exome Sequencing
~20,000 coding genes · 10 Gb
Reads the part of DNA where most known disease-causing variants sit, avoiding a gene-by-gene search.
Final price
$982 USD
- Sample
- Saliva or blood
- What it reads
- All protein-coding genes
- Best for
- Unexplained symptoms, a suspected rare disease, or family history that does not point to one gene.
Key points
- Broad inherited-DNA investigation in one assay
- Can power cancer, cardiology, neurology, and metabolic panels
- One report category included
Results in 25 business days
Physician involvement recommended
From sample to result
What every test includes
- DNA or RNA extraction and sample preparation
- Next-generation sequencing and bioinformatics
- Results in a secure portal with downloadable files
- One report category per sample at no extra charge
- Coordination for interpretation with a specialist
For WES and WGS, the same data can later power focused panels for hereditary cancer, cardiology, neurology, metabolic disease, and more than 100 other areas.
How it works
Supported from start to finish
- 01
Define the question
We confirm the test, sample type, and whether a physician's order is needed.
- 02
Collect the sample
Saliva or blood for germline tests; tissue, special blood tube, or RNA for tumor tests.
- 03
Sequence and analyze
The laboratory performs extraction, sequencing, and bioinformatics. Timing starts with a valid sample.
- 04
Review the result
You and your physician receive secure access; we can coordinate an interpretation session.
Technology and scientific alliances
Before you decide
Important scope and limitations
- A negative result does not rule out every possible genetic cause.
- Repeat expansions and some structural variants may not be fully assessed.
- Environment, lifestyle, and other genes also affect risk.
- Results are not a prescription and must not be used alone to change treatment.
- Speak with your physician or a genetic counselor before acting on any finding.
You do not have to choose alone
Tell us what you need to investigate and what sample is available. We will help you prepare the right questions for your physician.