Applications – Explore key insights in your field
In Focus – Discover latest updates & stories
- Explore a single unified solution that combines the precision of our panels with intuitive bioinformatics so you can detect, analyze and interpret low-frequency variants with confidence. Get targeted DNA panels plus analysis and interpretation software all in a single kit.
- Our digital PCR quiz is in full swing but will end soon. You can play once to earn points and have fun, or you can play multiple times to compete with your friends and coworkers, and increase your odds of winning our grand prize!
- Maximize your miRNA sequencing and qPCR success from liquid biopsy samples, including blood, serum/plasma, urine, CSF and exosomes. Find out how, plus get helpful tips and valuable advice in our guidelines for profiling biofluid miRNAs booklet. Download now.
- Download our new white paper to explore how Ingenuity Pathway Analysis can help you understand the biological mechanisms in transcriptomics or proteomics.
- Join our lunch symposium at the 2019 ISFG Congress, Prague. Learn how a new NGS workflow is enabling identification of missing persons and is bringing closure to families around the world. Register here!
Featured Products – See this week's favorites
The next generation of syndromic insights
Harness the full potential of multiplex syndromic testing and confidently provide clinical insights to patients with the highest level of versatility.
Ingenuity Pathway Analysis (IPA)
Understand complex 'omics data
Quickly understand and visualize data derived from ‘omics experiments, such as RNA-seq, small RNA-seq, microarrays including miRNA and SNP, metabolomics, proteomics, and small scale experiments.
RNeasy Mini Kit
High-quality total RNA in minutes
Obtain highest-quality RNA with minimum copurification of DNA using our popular RNeasy spin columns.
Redefining automated sample processing
Fully automate QIAGEN gold-standard spin-column purification procedures with the new QIAcube Connect instrument.
QIAseq Tumor Mutational Burden Panels
Precision genotyping for tumor mutational burden
Create a comprehensive profile of Tumor Mutational Burden and Microsatellite Instability with QIAseq panels and get unprecedented insight using QCI with the latest AMP/ASCO guidelines.
GeneReader NGS System
The first complete Sample to Insight NGS solution
Standardize your workflow to quickly and accurately identify the genetic markers associated with approved therapies, leading professional guidelines and active clinical trials.