Ebogenes Store
EBOGENES Xpert BCR-ABL Ultra PCR Test
EBOGENES Xpert BCR-ABL Ultra PCR Test
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Laboratory PCR test for BCR-ABL p210 transcripts, for clinics and healthcare professionals. Practitioner order required.
What it tests
BCR-ABL p210 transcripts
How it works
Practitioner orders the test → sample collected at the clinic → sample sent to the laboratory → PCR analysis → results reported to the ordering clinic
What's in the box
No kit shipped – sample collected by the ordering clinic
At a glance
- Sample: Peripheral whole blood
- Collection: Clinic
- Report time: 24 hours after the laboratory receives the sample
- Test type: Diagnostic
- Who it is for: Clinics and healthcare professionals
Storage & handling
Not applicable to patients – sample collected and handled by the clinic, per laboratory specimen-handling instructions.
Laboratory & report
All analyses are conducted in-house at the EBOGENES laboratory. Each final report is prepared by our science team and clinically reviewed by a licensed physician.
FAQ
Who can order this test? Clinics and licensed healthcare practitioners only. It is not available to the public.
What sample is required? Peripheral whole blood.
How fast are results? Results are available 24 hours after the laboratory receives the sample.
Who analyzes the sample? All analyses are performed in-house at the EBOGENES laboratory in Canada. Results are reported to the ordering clinic.
What happens to patient data? Patient data and results are stored in Canada and reported only to the ordering clinic. Data is handled in accordance with applicable privacy laws.
For professional use only. Results must be interpreted by a qualified healthcare professional in the context of the patient's clinical history. This test does not replace clinical judgment. BCR-ABL quantitative results should be reported on the International Scale (IS) where applicable. Handle samples in accordance with BSL-2 (or equivalent) biosafety requirements. Clinical diagnostic test – B2B only, not sold to consumers. Practitioner order required. Results must be interpreted by a qualified healthcare professional. BCR-ABL testing should be performed in laboratories participating in appropriate quality-assurance programmes.
Data stored in Canada (AWS ca-central-1).
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.