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Tests pharmacogénomiques
Tests pharmacogénomiques
Impossible de charger la disponibilité du service de retrait
Vous êtes-vous déjà demandé pourquoi un même médicament fait des merveilles chez certaines personnes, mais provoque de graves effets secondaires chez d'autres ? La réponse réside souvent dans les gènes. Votre patrimoine génétique influence la façon dont votre corps traite et réagit aux différents médicaments, influençant ainsi tout, de l'absorption et du métabolisme des médicaments à leur efficacité et leur toxicité.
La pharmacogénomique étudie l'influence des gènes sur la réponse aux médicaments et permet d'identifier les variations génétiques qui influencent leur métabolisme. Ces variations peuvent influencer l'efficacité d'un médicament, le dosage approprié et la probabilité d'effets secondaires. Ce test explore comment la pharmacogénomique peut personnaliser les choix de médicaments, optimiser les plans de traitement et réduire les effets indésirables. Cette approche aide les professionnels de santé à prescrire le médicament adapté à chaque individu, à la dose idéale et élimine les tâtonnements pour trouver le traitement optimal, garantissant ainsi un rétablissement plus rapide et plus sûr.
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.
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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.