Ebogenes Store
BabyDNA ID™
BabyDNA ID™
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BabyDNA ID—Your Newborn’s Lifetime Genetic Passport
Powered by Whole Genome Sequencing (WGS)
For Newborns—From Day 1, Know More.
Discover insights into over 2,500 genes linked to childhood-onset health conditions and drug sensitivities, using a single sample from your baby’s cord blood.
Why Choose BabyDNA ID?
47% of these findings are linked to conditions where early medical intervention can make a real difference.
What You Get:
Full genome sequencing of all ~22,000 genes
Focused analysis on 2,500+ clinically relevant genes
Identification of variants linked to:
• Inherited childhood disorders
• Immune system traits
• Nutrient metabolism
• Adverse drug reactions
Why It Matters:
• One-time test, insights for life
• Helps you nurture potential early—in learning, sports, nutrition, and behavior
• Gives your child a personalized head start in both health and talent development
• All data stays private and re-analyzable as science evolves
Ideal for:
• New parents seeking proactive health insights
• Families with history of genetic conditions
• Those storing cord blood who want to maximize its value
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.