Ebogenes Store
EboMedAI Subscription
EboMedAI Subscription
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Product Description:
EboMedAI Consultant is your personal AI-powered genetic consultant, designed by geneticists, medical doctors, bio-information experts, and AI scientists. It helps you interpret your genetic test results and understand potential health risks, variant significance, and lifestyle implications based on your DNA. Data Security Notice:To fully protect your privacy and comply with global genetic data safety standards, your uploaded report and genetic data are NOT stored on our servers. Therefore, please keep the session window open while interacting with the AI. If the page is closed or refreshed, you will need to re-upload your genetic report.
Key Features
· AI-powered analysis of your genetic report (e.g., EboGenes Genetic Report, Blueprint Report, AncestryDNA, whole exome, or genome)
· Purpose-Built for Genetics: Unlike generic AI like ChatGPT, EboMedAI is trained and fine-tuned by clinical geneticists, AI scientists, and physicians specifically for interpreting genetic data.
· Structured Variant Analysis: Automatically identifies and prioritizes clinically relevant mutations using 170+ global variant databases (ClinVar, gnomAD, HGMD, etc.).
· Personalized Health Risk Insights: Generates risk assessments based on genotype–phenotype relationships, with disease association scoring—not just generic text responses.
· Scientific Evidence Linking: Every interpretation includes references from over 35 million scientific and clinical publications—traceable and credible.
· Human-Centered Explanations: Translates complex variant data into plain language, helping users understand without a medical background.
· Report-Aware Conversations: Unlike ChatGPT, EboMedAI “remembers” your uploaded report structure throughout the session, allowing focused and context-aware answers.
· Privacy by Design: Your genetic data is never stored on our servers. All analysis runs in-session only. No uploads are saved, ensuring full data privacy compliance.
· Tailored Outputs: Offers downloadable, doctor-friendly summaries and variant-level insights that are not available through general AI tools.
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.