Accelerate test turnaround and enable confident decisions with expert-curated gene- and variant-level insights for NGS data interpretation and reporting
Across all genomic profiling applications, from research to molecular testing and pharmaceutical development, the ability to identify and interpret potentially actionable genetic alterations is becoming increasingly difficult. As NGS tests increase in size, more biomarkers are uncovered, and demand for routine testing soars, labs need the most up-to-date, biological and clinical information directly in their informatics pipeline to identify and classify variants rapidly and confidently.
Transform unstructured data into actionable insight. By aggregating, manually curating, and modeling scientific literature and professional guidelines with semantic consistency, QIAGEN Digital Insight’s portfolio of gene- and variant-level databases captures biological, phenotypic, therapeutic, and outcomes information that enable variant- and disease-specific classifications for every alteration in every disease for every patient case.
Overcome inefficiences in your drug development program with real-world genomic data and expert-curtated content to identify biomarkers, optimize study designs, and improve patient outcomes.
Accelerate test turnaround and enable confident decisions with expert-curated gene- and variant-level insights for NGS data interpretation and reporting for germline and somatic applications.
Translate samples into actionable insights and scientific breakthroughs with expert-curated databases to help you analzye, interpret, and report genetic variation and biological function.
High-touch, expert curation methods are essential to provide consistent and accurate biological and clinical variant interpretation. In this white paper, learn about the different methods of data curation for clinical NGS testing, best practices for incorporating data into clinical reports, and the value of combining automation and human judgment in decision-making.
Fill out the form to request a consultation with our clinical testing experts to learn more about our gene- and variant-level databases and which solution is right for your lab.
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Out-of-the-box and custom NGS panels enabling digital DNA and RNA sequencing to confidently detect low-frequency variants