You need confidence to beat cancer. But confidence by itself isn’t enough. It takes insight too. Being able to confidently interpret somatic and hereditary cancer variants and pair them with the right health options is critical for precision medicine to conquer cancer. QIAGEN® Clinical Insight (QCI™) gives you confidence plus insight.
Cancer moves fast, but we can move faster. NGS data interpretation no longer needs to be the rate-limiting step. Speed-up your turn-around-time and expand your NGS test menu and volume by streamlining your variant interpretation and reporting steps with QCI.Streamline your interpretation
Powered by the expertise of Ingenuity, CLC bio, and BIOBASE, combined with the stability of QIAGEN, QIAGEN Bioinformatics is your trusted partner. With the market’s most comprehensive biomedical content, more than 10 million findings in our QIAGEN Knowledge Base, and 16 years experience in manual curation, we have a reputation for gold-standards.Get experience now
Clinical labs rolling out NGS-based tests are confronted with two key challenges: the complexity of turning molecular profiling information into precise medical recommendations, and the time and effort it takes to generate actionable reports. QIAGEN Clinical Insight provides a rich and detailed, yet very clear and concise, report that suggests management and treatment options based on the patient’s gene variations that profile their disease and outline causal links. It is this kind of interpretation that gives clinical value to the data, and what enables the actual insights into a patient’s specific disease and treatment options.
Madhuri Hegde, PhD, FACMG
Professor of Human Genetics at the Emory University School of Medicine
and Executive Director of the Emory Genetics Laboratory
With QCI variants are automatically classified according to evidence-levels from professional guidelines, drug-labels, and clinical trials. To power your decision-making and support your validations we provide full transparency to the rules and allow you to customise if needed. We also curate the high-value clinical case counts and link directly to the source.Scale your interpretation with QCI™
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