
Transforming the claims experience for a Fortune 500 health insurer and their clients- to reduce costs, build trust and delivery timely accurate answers when it matters most.
Transforming the claims experience for a Fortune 500 health insurer and their clients- to reduce costs, build trust and delivery timely accurate answers when it matters most.
Pharma companies use science-based innovations, analytical tools, and services to give out answers to some of the most challenging healthcare problems.
They help people live a long and healthy life. One such Fortune 500 pharma company wanted to analyze the biomarker data and unmined clinical trial. Modak Analytics, along with a consultant team, undertook this transformation. There were many challenges:
Modak developed a system for integrating new studies that have already been standardized to SDTM (Study Data Tabulation Model) format. This helps to scale the larger number of legacy studies that could not be addressed and where ETL and statistical programming could not keep up. Modak combined machine learning and expert analytical tools to map legacy clinical trials to the master schema by:
Modak’s Novel approach of preparing data for downstream analytics enables scientists to access more data to make better, faster, and more accurate decisions. Moreover, it enables biopharmaceutical organizations to finally see a return on their enormous data investment.
A genome-wide association study (GWAS) is a genetics research method for linking specific genetic variants to specific diseases. The procedure entails scanning the genomes of a large number of people in order to find genetic markers that can be used to predict the existence of disease.
This study helps to develop customized medicines depending on various factors that affect the subject, thereby reducing the risk of side effects and increasing the effectiveness.
The blood samples from two similar bodies are taken, of which one is affected by disease and the other is not. Then, the DNA of the subjects is collected from the blood samples and further study of the structures is done by trying to find the SNPs. Then those gaps are studied thoroughly, and a solution is found.
This process requires fewer human resources. Hence, it is cost-effective. Here, precision is the key to success. Even a small calculation error can cost lives.
We use CUDA libraries to leverage GPU acceleration and harness the enormous computing power of Nvidia’s graphics processing units. Our tools are built to run on a GPU cluster and try to exploit the massively parallel architecture of GPUs.
OpenMPI and Nvidia’s NCCL and NVBLAS libraries have been used to achieve this feat. We also support the OpenCL platform using ArrayFire’s OpenCL at the backend.