Here is short details about our institute, Also you can see how we work
A genome is the complete set of genetic material (DNA) in an organism. In humans, this means all the DNA found in nearly every cell of the body. DNA (deoxyribonucleic acid) is like a biological instruction manual. It tells our bodies how to grow, function, and stay healthy.
Each human genome contains about 3 billion DNA base pairs, organized into 23 pairs of chromosomes—one set from your mother and one from your father.
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Risk awareness tools
Diagnostic pathways
Family-centered support resources
Translated educational materials

National and regional clinical guidelines
Training videos and CPD modules
Referral forms and diagnostic charts
Downloadable toolkits for practice

Partner portals for data sharing
Webinars and online symposia
Joint university research projects
Co-authored case studies and findings

Comics and explainer videos
Myth-busting articles
Community engagement guides
Public education campaigns
Collecting and analyzing genetic data isn’t just science — it’s sacred.
At East Africa Genome, we know we’re not just working with samples — we’re working with stories, with identity, with trust.
That’s why ethics is at the heart of everything we do:
We believe in genomic justice — where communities benefit from the research, not just outsiders.
Science without ethics is exploitation. But with integrity, it becomes liberation.
Healthcare doesn’t stop at borders. Neither do genetic conditions.
A disease common in northern Kenya may also be found in southern Ethiopia or western Somalia.
That’s why EAG works across all of East Africa — uniting labs, hospitals, universities, and governments.
Our work is regional because:
By creating a shared genomic ecosystem, we increase our bargaining power, improve health equity, and give every East African country a seat at the table.
East Africa united in science is East Africa stronger in health.
In many East African cultures, inherited conditions are misunderstood.
Families are blamed. Children are shamed. Women face stigma for having a child with a disability.
But genetic disorders are not anyone’s fault. They’re biological, not personal.
That’s why EAG is investing in community awareness and culturally sensitive counselling.
We help families understand their genetics. We train counsellors who speak local languages and understand local realities.
Our goal? A society where talking about genetics isn’t taboo — it’s empowering.
No one should suffer in silence.
Let’s replace shame with science. And blame with knowledge.