explanation
NxClinical is the name of the most comprehensive, state-of-the-art solution for cytogenetics and molecular genetics in systems that analyze and interpret all genetic variants in microarray and NGS data. This program was developed by: discovery of life ,The first step is to detect CNVs. You can’t sense what you can’t see. NxClinical is the gold standard for CNV recall in NGS and microarray data generated on each platform. The program can integrate and visualize raw data from CNV, SeqVar, and AOH simultaneously. It also allows you to make the right call at the right time. A wide range of artificial intelligence and automation tools are also available for fast and accurate interpretation. Additionally, active links to the latest databases keep your basic knowledge up to date.
NxClinical Features:
- Increase case review efficiency with multiple detail pages.
- Build your own knowledge base that stores genetically diverse regional information
- Build and use genome-wide CNV and AOH profiles for various types of cancer to help diagnose and interpret tumors.
- Automated disease sample recording and integrated genetic database eliminate the need to discard outdated data.
- NxClinical is compatible with a variety of platforms.
- Multi-user system with global audit and access capabilities
- Security – Supports data quality and integrity
- Select Speed – Accelerate TAT faster using automation, artificial intelligence, and variable prioritization tools.
- Improved clinical utility and diagnostic efficiency
system needed
NxClinical is technology and platform agnostic. Processes both microarray and NGS data. Supported as well as custom platforms from major manufacturers including Illumina, Thermo Fisher (Affymetrix), and Agilent. You can load and analyze data from any manufacturer/platform in the same database.
movie
installation manual
Please read the Readme.txt file.
download link
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size
2.3GB