After evaluating SEDGE for the use in genomics applications we believe it offers a powerful tool for big data management. It gives user the ability to merge the data and use SEDGE's innovative approaches for data analysis and visualization. This enables discovery of novel patterns in the data, which we feel is particularly useful in clinical trials and drug discovery processes.
SEDGE ASSISTED BioSistemika
A software development partner for a life sciences company to analyze clinical data that
investigated the risk of optic pathway glioma (a malignant tumor of the nervous system) in
patients with type I neurofibromatosis (tumor disorder caused by the mutation of a gene)
IDENTIFICATION OF TWO NEW GENE VARIANTS
SEDGE helped identify two new gene variants as recognized biomarkers for glioma
in genes. SEDGE was able to establish this dependency just by analyzing data with no prior
domain knowledge of the biological problem. These results are very valuable to the BioSistemika’s client to conduct further focused research.