The recent explosion in the use of next-generation sequencing in the study of human disease
has led to an exponential rise in the number of publications on the subject.
With the burden of manual curation dramatically increasing, extracting valuable and up-to-date
variant information is now a daunting task.
Transform how you find answers with
QIAGEN Clinical Insight
Transparent, evidence-sourced NGS variant calling, interpretation and reporting
QCI automates variant classification with full transparency to the supporting evidence sourced
from the QIAGEN Knowledge Base–the largest, most-up-to-date clinical database
with over 16 million biological findings and over 1 million processed human samples.
Offering the highest level of interpretation transparency currently available in the market, QCI Interpret displays every piece of supporting evidence included in the interpretation process.
The software is connected to the QIAGEN Knowledge Base, the industry’s largest, most-up-to-date clinical database with over 16 million biological findings.
Pulling data from clinical trials, case studies, peer-reviewed literature, drug labels, external databases, professional guidelines, and the direct experience of interpreting over 1 MILLION human samples, the QIAGEN Knowledge Base is unrivalled in clinical breadth and depth.
Try QCI Interpret
Request your free, no obligation, demonstration of QCI Interpret today.
*QIAGEN Clinical Insight (QCI) is an evidence-based decision support software intended as an aid in the interpretation of variants observed in genomic sequencing data. The software evaluates genomic variants in the context of published biomedical literature, professional association guidelines, publicly available databases and annotations, drug labels, and clinical-trials. Based on this evaluation, the software proposes a classification to aid in the interpretation of observed variants. The software is NOT intended as a primary diagnostic tool by physicians or to be used as a substitute for professional healthcare advice. Each laboratory is responsible for ensuring compliance with applicable international, national, and local clinical laboratory regulations and other specific accreditations requirements.