GenterpretR
www.genterpretr.comGenterpretR 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 moreGenterpretR 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 moreCountry
State
Texas
City (Headquarters)
Austin
Industry
Employees
1-10
Founded
2020
Social
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View all employeesPotential Decision Makers
Co - Founder and Chief Scientist
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