GenterpretR

www.genterpretr.com

GenterpretR is aiming for personalized healthcare researches. It is based on UK, USA, and UAE. WE HELP HARNESS THE POWER OF GENOMIC ANALYSIS: We work with hospitals, drug-makers, clinicians, and biomedical scientists to help them dive into the wealth of information residing inside large volumes of genetic readouts. We specialize in applying cognitive computing and deep learning approaches to link genotype with phenotype. We also establish bespoke bioinformatics pipelines and scalable machine learning/statistical algorithms to enable the integration and processing of clinically relevant multi-omic datasets. WE BELIEVE IN PROVIDING PERSONALIZED CARE FOR ALL: Every genome represents substantial exclusivity, which tells about its disease predispositions and vulnerabilities. We are building applications that connect genomic data with drugs' structural attributes to infer drug response. Our proprietary APIs can easily be integrated with clinical decision management systems to make personalized therapy a reality. WE DECODE THE UNDERLYING MYSTERY OF RARE DISEASES: The genotype-phenotype association remains to be an unsolved puzzle. Genomic alterations are sparse, obscuring our understanding of the cause of rare diseases. This also hinders treatment decision-making for complex diseases such as cancers. Our in-house AI toolbox enables vector embedding of mutations by ingesting volumes of mutation data, thereby enabling the identification of causal mutations without requiring a large sample size.

Read more

Reach decision makers at GenterpretR

Lusha Magic

Free credit every month!

GenterpretR is aiming for personalized healthcare researches. It is based on UK, USA, and UAE. WE HELP HARNESS THE POWER OF GENOMIC ANALYSIS: We work with hospitals, drug-makers, clinicians, and biomedical scientists to help them dive into the wealth of information residing inside large volumes of genetic readouts. We specialize in applying cognitive computing and deep learning approaches to link genotype with phenotype. We also establish bespoke bioinformatics pipelines and scalable machine learning/statistical algorithms to enable the integration and processing of clinically relevant multi-omic datasets. WE BELIEVE IN PROVIDING PERSONALIZED CARE FOR ALL: Every genome represents substantial exclusivity, which tells about its disease predispositions and vulnerabilities. We are building applications that connect genomic data with drugs' structural attributes to infer drug response. Our proprietary APIs can easily be integrated with clinical decision management systems to make personalized therapy a reality. WE DECODE THE UNDERLYING MYSTERY OF RARE DISEASES: The genotype-phenotype association remains to be an unsolved puzzle. Genomic alterations are sparse, obscuring our understanding of the cause of rare diseases. This also hinders treatment decision-making for complex diseases such as cancers. Our in-house AI toolbox enables vector embedding of mutations by ingesting volumes of mutation data, thereby enabling the identification of causal mutations without requiring a large sample size.

Read more
icon

Country

icon

State

Texas

icon

City (Headquarters)

Austin

icon

Employees

1-10

icon

Founded

2020

icon

Social

  • icon

Employees statistics

View all employees

Potential Decision Makers

  • Co - Founder and Chief Scientist

    Email ****** @****.com
    Phone (***) ****-****

Reach decision makers at GenterpretR

Free credits every month!

My account

Sign up now to uncover all the contact details