Implementing a precision medicine platform is
within reach with Genotech Matrix
NGS Analytical Toolkits
A set of software modules that analyze a DNA sequence for variant mutations to produce a variant calling file. This VCF is then uploaded into the precision medicine platform workflow and compared with the information contained in the knowledge base to generate the patients individualized report. A complete set or individual modules are available for various types of analyses.
NGS Analytical Toolkits carry out analysis for:
Single nucleotide polymorphisms
Copy number variations