Genuity Science

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Genuity Science is a wholly-owned subsidiary of US biotechnology company, HiberCell. Genuity Science is using world-leading genomics and machine learning to map the causal biology of disease and accelerate the development of better medicine. Our unique hybrid platform enables us and our partners to go from data to insights to impact with unrivaled power and efficiency, generating, validating and applying insights on virtually any disease to create novel drugs, diagnostics and tools for clinical care. Our capabilities span deeply phenotyped population genomics cohorts, CAP-accredited sequencing and comprehensive omics, world-renowned bioinformatics, and pioneering, validated and peer-reviewed AI/ML. Through our offices in Boston, Dublin and Reykjavik we put this platform to work for our global biopharma and life sciences partners and the patients they serve. To learn more, visit us at www.genuitysci.com.

Company Details

Employees
22
Founded
-
Address
90 Canal St, Boston,massachusetts 02114,united States
Phone
617-250-3500
Email
sa****@****sci.com
Industry
Biotechnology Research
NAICS
Research and Development in Biotechnology (except Nanobiotechnology)
HQ
Boston, Massachusetts
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News

Ionis and Genuity Science announce agreement designed to rapidly translate genomic insights into therapeutics - PR Newswire

Ionis and Genuity Science announce agreement designed to rapidly translate genomic insights into therapeutics PR Newswire

Editorial: Improving medical diagnosis in rare diseases - Frontiers

Editorial: Improving medical diagnosis in rare diseases Frontiers

The Future of Genomic Medicine - Genetic Engineering and Biotechnology News

The Future of Genomic Medicine Genetic Engineering and Biotechnology News

Accelerating the Translation of Genomic Insight to Therapeutics - Genetic Engineering and Biotechnology News

Accelerating the Translation of Genomic Insight to Therapeutics Genetic Engineering and Biotechnology News

Uniparental disomy screen of Irish rare disorder cohort unmasks homozygous variants of clinical significance in the TMCO1 and PRKRA genes - Frontiers

Uniparental disomy screen of Irish rare disorder cohort unmasks homozygous variants of clinical significance in the TMCO1 and PRKRA genes Frontiers

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