NGS sequencing software BioVisor© NGS

laboratorydata analysismanagement

The BioVisor NGS software allows to manage the variants obtained through exomic sequencing. The application allows the study of multigene-based diseases, hereditary cancer, tumor tissue, exome comparison for the study of index cases and the study of the cause of repeated miscarriages, among other specifications. The BioVisor NGS automatically analyses and interprets the genetic data and it identifies the mutations related to the pathology. In addition, it allows the data filtering based on the user's criteria, the management of the local variants and networking. The application operates locally, so that genetic data, analysis and reports are exclusively in the user's facilities. Security - Users and permissions management. - Register of activity of each user. Gens panels - Design of gene panels according to the user's criteria. - Automatic interpretation of the result - Manual filters for data screening. - Re-analysis of previous genetic studies. Exome comparison - Detection of mutations in index cases. - Study of de novo mutations. - Study of the genetic basis of repeated miscarriages. Cancer - Genetic study of hereditary cancer. - Study of alterations in tumor DNA. Other features - Local database. - Management of local mutations and polymorphisms. - Networking. Results report - Issues a pdf file with the results.