HGMD Professional
Solve more cases faster, with data you can trust using HGMD Professional, the de facto standard resource for identifying inherited disease-causing mutations.
Founded and maintained by the Institute of Medical Genetics at Cardiff University in 1993, HGMD Professional contains over 260,000 manually curated mutation reports from over 2,600 peer-reviewed journals. Updated quarterly, HGMD Professional is licensed exclusively through QIAGEN and offers clinical research labs pipeline access to the latest reports of all published inherited disease mutations.
Read more >QCI Analyze
Simplify and standardize the processing and analysis of NGS data with QIAGEN Clinical Insight (QCI®) Analyze, scalable software fueled by powerful algorithms to seamlessly convert FASTQ files to high quality variant lists.
Compatible with all major sequencing platforms, QCI Analyze efficiently converts FASTQ files to VCF files through preconfigured, comprehensive and scalable pipelines controlled by role-based permissions. The software uses powerful, globally recognized algorithms to pinpoint even the most difficult-to-detect variants and fusions.
Read more >Ingenuity Variant Analysis
Quickly prioritize variants with Ingenuity Variant Analysis, a web-based application combining analytical tools and expert-curated content from the QIAGEN Knowledge Base to help you filter down to a small, targeted subset of compelling candidates.
Connected to the industry’s most expansive collection of biological and clinical findings, sourced from over two decades of manual data and literature curation from more than 40 scientific and clinical databases, Ingenuity Variant Analysis leverages powerful algorithms and dynamic filtering to triage variants using both published evidence and your lab’s own experiential knowledge.
Read more >QCI Interpret
Clinical decision support software integrated with the industry’s largest knowledge base, QCI Interpret reproducibly translates highly complex next-generation sequencing (NGS) data into concise, clinician-ready reports, using current clinical evidence and automated guidelines from AMP/ASCO/CAP and NCCN for the assessment of sequence variants in cancer.
Connected to the QIAGEN Knowledge Base, a continuously updated and manually curated resource spanning across 40 public and proprietary databases, QCI Interpret empowers your lab with the insight only two decades of expert curation can deliver.
The software provides full transparency to review the criteria and evidence supporting each classification and allows you to customize an actionable report from the latest scientific literature, clinical trials and approved drug labels.
Read more >QIAGEN Clinical Testing Services
Accelerate time to launch with clinical testing and informatics services focused on expanding and differentiating your test menu.
QIAGEN Clinical Testing Services deliver complete end-to-end testing solutions, fully customizable and capable of supporting a broad range of indications both now and in the future.
- On-demand variant scoring and classification services Launch new test offerings faster while scaling your existing variant scientist team.
- Customized reporting solutions Provide unique and differentiated report layouts for brand recognition.
- Pipeline development and optimization Rely on one partner to monitor, develop and train your bioinformatics team.
