TestEasy
Xpress HPV qPCR Test (includes Consultation with our partner health professional)
Xpress HPV qPCR Test (includes Consultation with our partner health professional)
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NOTE: Doctor's prescription needed
Call us (+1 450-688-8377 ext. 2209) to be connected with a physician.
Price includes both consultation and procedure
- Included consultation with our partner health professional (valued at $150)
- Same-day Result after sample reception
- Fast results compared to the public sector
- Receipt for insurance claim included
Detection of High-Risk HPV DNA with Genotyping
Based on the GeneXpert® technology, Xpert HPV automates the test process, including DNA extraction, amplification, and detection, in one fully integrated cartridge.
On-demand HPV testing—a next-generation solution:
- Highest risk HPV 16 and HPV 18/45 call-outs enhances patient management
- Optimized detection of 14 hrHPV reported as HPV16, HPV18/45, or other hrHPV (31, 33, 35, 52, 58; 51, 59; 39, 56, 66, 68)
- E6/E7 oncogenes target eliminates concerns in case of L1 gene deletion.
- Sample adequacy control (SAC) confirms patient sample contains human DNA
- HPV results in around 60 minutes for same-visit clinician/patient consult, minimizing need for repeat visits
All 6.4 billion letters of your DNA — read, stored, and yours to keep.
Most consumer DNA tests sample a few hundred thousand positions. Whole genome sequencing reads the entire thing at 30× depth, and hands you the files at the end. No subscription required to keep them.
-
30×
average
coverage depth -
6.4B
base pairs
sequenced -
FASTQ
BAM & VCF
files included
How it runs
Kit arrives
Day 0，Saliva collection takes about five minutes. Avoid eating, drinking, or brushing your teeth for thirty minutes beforehand — that's the only preparation required.
Sample ships back
Day 1–2， Prepaid return envelope is included. Saliva samples are stable at room temperature, so there's no cold chain to manage on your end.
DNA extraction and quality check
Week 1，We extract and assess DNA quality before sequencing. If a sample fails QC, we send a replacement kit at no charge rather than sequencing something that won't yield reliable calls.
Sequencing and analysis
Week 2–6，Sequencing, alignment to GRCh38, and variant calling. This is the longest stage and we'd rather state it accurately than quote a number we miss.
Reports and files released
Week 2–6， Your reports and all three file formats become available together. You'll get an email the moment they're ready.
No. Ebogenes whole genome sequencing is offered for research and personal informational use. It is not a diagnostic test, it is not a substitute for clinical genetic testing, and it should not be used to make medical decisions on its own. If a finding concerns you, bring it to a physician or a certified genetic counsellor — that's what the files are for.
Each position in your genome is read approximately thirty times on average. Sequencing makes errors, so reading a position once tells you little; reading it thirty times lets a variant call rest on consensus. 30× is the widely used standard for reliable variant calling — below it, calls get noticeably less dependable.
Our reports flag findings for follow-up; they do not diagnose. A variant of uncertain significance is a flag, not a finding — many are later reclassified as benign. We'd rather tell you plainly that something needs a professional look than dress up an uncertain result as an answer.
Sequencing and storage happen at our Laval, Québec facility. Your data stays in Canada and is subject to Canadian privacy law. We do not sell your genetic data, and we do not share it with insurers, employers, or research programmes without your explicit, separate consent. You can request deletion at any time.
No. Your reports and all three file formats remain accessible without any ongoing payment. Download them and store your own copy if you prefer — that's the point of giving you FASTQ.