Human Healthcare 2017-07-11T11:39:26+00:00

Human Healthcare

Enabling Personalized Medicine on a Large Scale

Diseases like cancer, Alzheimer’s or Multiple Sclerosis all have a genetic element. They are all hard to treat, partly because of the genetic differences among individual patients. Each of us has a unique genetic makeup. The genetic differences give rise to variances in disease susceptibility and treatment response.

Medical centers and R&D in biotech and pharma are adopting genomics-based discovery programs to accelerate disease research. The entire genomes of hundreds of thousands of individuals are sequenced annually, creating huge amounts of data, while incurring significant costs.

What is missing is a tool which can accurately reveal and map relevant genetic differences from big data, cross-referencing it to clinical data, to find the relationship between genetics and disease. Due to the complexity of the problem and the database size, many of today’s tools provide an inaccurate or distorted picture.

NRGene’s cloud-based, analytic genomic Big Data solutions solve complex genetic challenges by combining very large human genome databases, reducing the need to sequence data along with the associated costs and time by a factor of 10. Our unique tools were tested and found to be the only ones which can accurately phase the genomic data, correctly separating between genes inherited from the paternal and maternal lines and creating correct haplotypes.

GenoMAGIC, NRGene’s analysis platform, leverages big data analytics to reduce the number of sequencing cycles needed to get full genome resolution. It accurately reveals genomic diversity among individuals and correlates them to their medical data to uncover variations associated with clinical features and drug response.

EMAIL US
DOWNLOAD BROCHURE

Human Healthcare

Enabling Personalized Medicine on a Large Scale

Diseases like cancer, Alzheimer’s or Multiple Sclerosis all have a genetic element. They are all hard to treat, partly because of the genetic differences among individual patients. Each of us has a unique genetic makeup. The genetic differences give rise to variances in disease susceptibility and treatment response.

Medical centers and R&D in biotech and pharma are adopting genomics-based discovery programs to accelerate disease research. The entire genomes of hundreds of thousands of individuals are sequenced annually, creating huge amounts of data, while incurring significant costs.

What is missing is a tool which can accurately reveal and map relevant genetic differences from big data, cross-referencing it to clinical data, to find the relationship between genetics and disease. Due to the complexity of the problem and the database size, many of today’s tools provide an inaccurate or distorted picture.

NRGene’s cloud-based, analytic genomic Big Data solutions solve complex genetic challenges by combining very large human genome databases, reducing the need to sequence data along with the associated costs and time by a factor of 10. Our unique tools were tested and found to be the only ones which can accurately phase the genomic data, correctly separating between genes inherited from the paternal and maternal lines and creating correct haplotypes.

GenoMAGIC, NRGene’s analysis platform, leverages big data analytics to reduce the number of sequencing cycles needed to get full genome resolution. It accurately reveals genomic diversity among individuals and correlates them to their medical data to uncover variations associated with clinical features and drug response.

EMAIL US
DOWNLOAD BROCHURE