Discover how CLC continues to improve and develop new capabilities. We’re excited to reveal many new improvements and enhancements to…

Two expert-curated databases exclusively licensed through QIAGEN link sequence-level somatic mutation data to detailed molecular information about functional and clinical…

With recent announcements of software retirements in the clinical NGS industry, many clinical diagnostic labs are looking for new variant…

Here’s the scenario – You’re a passionate scientist in a leading pharmaceutical company hoping to uncover a transformative drug candidate….

Let us help you bridge the gap between data quality and meaningful insights If you’re working in pharma or biotech,…

Become a pathway analysis expert with these powerful tools you didn’t know about We’ve all been there. Huddled over a…

In its latest release, QCI Interpret advances market-leading NGS interpretation software with artificial intelligence-driven insights to enable clinical exome completeness…

Interpretation of genomic variants in tumor samples still presents a challenge in clinical settings. Variant interpretation is fragmented across disparate…

Open-sourced software comes with a variety of risks. To more effectively advance your research, here’s where to turn instead. “Download…

We unite with ATCC to deliver a transformative database of authenticated cell ‘omics data What powerful partnerships come to mind…

QCI Interpret for Oncology will support the Danish National Genome Center’s new national initiative—one of Europe’s largest precision oncology projects…

Ready for a powerful biomedical data source that outperforms off-the-shelf consumer search AI? Look no further. We’ve got the fit…