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Nostos Genomics

AI-driven genetic analysis platform

Nostos Genomics logo
21-100 employees
  • Healthcare
  • B2B
  • Artificial Intelligence
Charlottenburg, Berlin, Germany

Company mission

To help people with genetic diseases to start a new journey.

Our take

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. Nostos Genomics is an AI-driven genetic analysis platform that enables genetic testing labs to give more people a clear and fast diagnosis.

The platform’s AI solution “AION” automatically identifies pathogenic variants and genetic mutations through leveraging a combination of machine learning and functional genomics. Typically, the average diagnosis time for these tests is 4-5 years, but sometimes patients can be looking at closer to a decade. This lead time paired with extensive and expensive workups and testing is telling of how transformative Nostos Genomics technology can be.

The company recently received a new influx of funding which it hopes to put towards quickly expanding the team, entering a series of new markets including the US, and conducting more studies to further develop its platform.

Kirsty headshot

Kirsty

Company Specialist at Welcome to the Jungle

Benefits

  • Develop your personal skills and knowledge with resources like books and courses to learn continuously.
  • Dynamic and flexible work environment that you can design (incl. remote work options).
  • Participate in our success with equity options.
  • Possibility to grow with the company and influence our direction.
  • Regular social activities: participate only if you feel like it.
  • Car allowance + flexible travel reimbursement.

Company values

  • Transparency
  • Kindness
  • Ownership
  • Personal growth

Funding (1 round)

Feb 2022

$5.2m

SEED

Total funding: $5.2m

This company has top investors

Leadership

Started their career as a Medic in the Swiss Armed Forces went onto Found and Direct START Hack for START Global. Also worked in Business Development for Merantix and a Research Assistant for Centre for Digital Health Interventions.

12+ years of research experience in genetic disease and expertise in state-of-the-art genomic and sequencing technologies. Most recently working as a Postdoctoral Researcher for Max Planck Institute for Molecular Genetics and becoming a Member of the Medical and Scientific Advisory Board for both SETBP1 Society and The Schinzel-Giedion Syndrome Foundation.