About 475 million people, or 10 percent of the world's population, suffer from rare diseases, and over 80% of them are genetic in nature.
The average time to diagnosis is seven years - the so-called diagnostic odyssey. This places a considerable burden on patients and their families.
We aim to pave a way forward by improving the accuracy, speed and accessibility of genetic testing, providing patients with the right information at the right time and empowering them to make informed health decisions.
Recent developments in genetic sequencing technologies have revolutionized genomics, and developments expected in the coming years will make it an essential part of medicine.
As genetic testing becomes more widespread in healthcare, the interpretation of the vast information it provides has become the biggest bottleneck in extending it to more patients and healthcare systems.
That’s where our journey started.
Our team reflects the interdisciplinary collaboration required to solve this grand challenge - from software and data science to genetics and healthcare.
Co-Founder & CTO
Machine Learning Scientist
Co-Founder & CEO
COO
Product Manager
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Product Marketing Manager
Human Genomics Scientist
Front-end Tech Lead
Head of Regulatory Affairs
Senior Human Genomics Scientist
Front-end Engineer
Senior Product Designer
Business Operations
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Lead QA Engineer
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People & Culture Associate
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Senior Software Developer
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Founder's Associate
Clinical Customer Success Manager
VP of Engineering
Head of Product
Frontend Software Engineer
Regulatory Affairs Specialist
Software Engineer - Backend Tech Lead
Backend Software Engineer
Elgar Fleisch, PhD
PROF. OF INFORMATION MANAGEMENT, ETH ZURICH & PROF. OF TECHNOLOGY MANAGEMENT, UNIVERSITY OF ST. GALLEN
Martin Kircher, PhD
GROUP LEADER IN COMPUTATIONAL GENOME BIOLOGY, BERLIN INSTITUTE OF HEALTH, CHARITÉ BERLIN
Lea Starita, PhD
ASSISTANT PROF. AT DEPARTMENT OF GENOME SCIENCES, UNIVERSITY OF WASHINGTON
Han Brunner, MD, PhD
PROF. OF HUMAN GENETICS, RADBOUD MEDICAL CENTER & HEAD OF CLINICAL GENETICS, MAASTRICHT UNIVERSITY MEDICAL CENTER
Join us in leveraging the power of artificial intelligence in genomics to enable fast and accurate diagnosis.
We are a proud, diverse, international group of creative problem solvers and humble learners who care about making a positive impact on society and are also aware of the trust placed in us.
For this reason, we value transparency, kindness as well as personal responsibility and encourage your personal growth.
Download our white paper to find out how AION’s white-box approach can help you to improve the quality and throughput of your variant interpretation.
Contact us!
*Nostos Genomics regularly produces webinars, white papers, and other types of content that you may find valuable.
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