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Interpretation and Reporting

With over 3 million NGS patient test cases interpreted worldwide, QIAGEN’s trusted portfolio of clinical interpretation and reporting solutions delivers the molecular insight you need to make confident decisions for every patient, every time.
Interpretation and Reporting Solutions
QCI Interpret for Oncology
Clinical decision support software for variant interpretation
and reporting for somatic NGS testing
QCI Interpret for Hereditary
Clinical decision support software for variant interpretation
and reporting for germline NGS testing
QCI Precision Insights
Clinical decision support software with on-demand expert services for variant interpretation and reporting for somatic NGS testing
Live Panel Discussion: September 30

Mitigating variability in somatic NGS interpretation

As NGS is increasingly used in precision oncology, there is an industry-wide issue of standardization: a high degree of variability in variant interpretation currently exists across laboratories. On September 30, in a live panel discussion, experts in NGS testing and clinical informatics explore the issues surrounding  standardization and how to overcome them with real-world applications. 

Related Clinical NGS Testing Solutions

Gene Variant Databases

NGS Secondary Analysis

Software for TSO500

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