Interpretation of the results obtained with molecular microbiology products
(RealCycler)
Interpretation of the results obtained with genotyping products
(RealType)
Analysis of variants obtained through NGS sequencing
Support software for RealCycler products
BioVisor Pro-Q software makes it easy to interpret results obtained with RealCycler products for pathogen detection and quantification.
BioVisor Pro-Q imports fluorescence data from the PCR equipment in real time, automatically analyzes it and generates a report with the result.
The application is validated for the Andana 1216, Quantstudio 5 (ThermoFisher Scientific), CFX96 (Bio-Rad), ABI7500 (ThermoFisher Scientific) and MIC (Biomolecular Systems).
-Users and permissions management.
- Compatible with several of the most used Real-time PCR instruments.
- Data import from the PCR instrument.
- Data import directly from the intranet (enabled devices only).
-Interpretation of each sample's results.
- Validation of each sample's results.
- Interpretation of the series according to the result of the controls.
- Analysis of several RealCycler reagents simultaneously.
-Monitoring of possible inhibitions.
-Archive of work series.
- Simultaneous quantification of several pathogens.
- Automatic calculation of the pathogen load in the sample.
- Conservation of the standard lines.
- Generate pdf, csv or excel files with the results.
- Export of results to LIS.
Support software for RealType products
The BioVisor RT software facilitates the interpretation of the results obtained with RealType products for the study of point mutations through genotyping tests by real-time PCR.
BioVisor RealType imports the fluorescence data from the Real-Time PCR instrument, analyses them automatically and generates a report with the result.
The application is validated for the instruments CFX96 (Bio-Rad), Quantstudio 5 (ThermoFisher Scientific), ABI7500 (Life Technologies) and MIC (Biomolecular Systems).
Application for the management of variants obtained by exome sequencing
The BioVisor NGS software allows to manage the variants obtained through exomic sequencing. The application allows the study of multi-gene-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.
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.
- Users and permissions management.
- Register of activity of each user.
- 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.
- Detection of mutations in index cases.
- Study of de novo mutations.
- Study of the genetic basis of repeated miscarriages.
- Genetic study of hereditary cancer.
- Study of alterations in tumor DNA.
- Local database.
- Management of local mutations and polymorphisms.
- Networking.
- PDF file with the results.