QCI Interpret Translational (QCIT) is a software designed for the assessment of variant loci in next-generation sequencing (NGS) data. It allows for rapid variant annotation, filtering, and selection, making it suitable for sequencing data such as Whole Exome Sequencing (WES) and Whole Genome Sequencing (WGS). By integrating with the QIAGEN knowledge database, QCIT can swiftly identify the most important disease mutations within human sequencing data. QIAGEN's knowledge database is one of the largest in the industry, gathering approximately 2 million unique variant loci from over 300,000 scientific articles. The QCIT system also provides a user-friendly filter interface, enabling users to filter based on variant loci of interest or research topics, allowing for quick focus on essential genes for subsequent experiments or reporting.

●Customized filtering and analysis
●Precise variant locus annotation
●Rich knowledge database
●Research report table generation
●Team collaboration and data sharing