New! QIAseq Pan-cancer Multimodal Panel for comprehensive genomic profiling of solid tumors and heme malignancies
Experience our innovative, single-day sample to sequencing workflow for simultaneous enrichment and profiling of 605 relevant DNA variant and RNA fusion biomarkers found across multiple cancers, as well as assessment of tumor mutational burden (TMB) and microsatellite instability (MSI), from a single sample input of 10 ng.
QIAseq Pan-cancer Multimodal Panel
Unlock insights into multiple cancers with just 10 ng total nucleic acid input.
-
Achieve high-confidence data
- Detect rare variants
- Reduce index hopping and read mis-assignment
-
Get complete coverage
- Find known and novel fusions
- Cover GC-rich regions
- Superior customization
-
Save sample, time and costs
- Multiple insights from a single extraction and workflow
- Reduce turnaround time and costs by 50%
Explore the 605 loci, 1.44 Mb panel
Explore this unique, one-day workflow
Experience our oncology solutions
-
Other QIAseq Multimodal Panels
- QIAseq Lung Multimodal Panel
- QIAseq Leukemia Multimodal Panel
- QIAseq Sarcoma Multimodal Panel
-
Nucleic acid isolation
- AllPrep Kits
- QIAamp DNA and QIAamp RNA Kits
-
Bioinformatics
- Pre-optimized secondary analysis with QIAGEN CLC Genomics Workbench
- Pre-configured variant interpretation with QIAGEN Clinical Insights for QIAseq
Watch the webinars
-
Single NGS workflow for DNA and RNA analysis from a single sample
In this webinar, Dr. Herold will discuss how her team has streamlined the profiling of cancer-associated alterations by using a single workflow for the construction of libraries from total nucleic acids for sequencing on Illumina platforms to achieve high operational efficiency.
-
Part 1: One-day workflow for simultaneous profiling of DNA variants and RNA fusions
In this webinar, we explore a new workflow for simultaneous NGS profiling of both DNA variants and RNA fusions, as well as gene expression in just one day, using as little as 10 ng sample.
-
Part 2: Curated panels and custom workflows for profiling DNA and RNA biomarkers in parallel
In this webinar, we will take you through an introduction and live demo of the QIAGEN CLC Genomics Workbench workflow for multimodal analysis. Discover this intuitive yet powerful solution tailored for analysis of NGS data generated with QIAseq Multimodal Panels.
-
Evolution of tumor profiling in a clinical lab
In this webinar, Vincent Funari of NeoGenomics will discuss how his team has evolved its profiling approaches for both heme and solid tumors from targeted panels to more comprehensive genomic profiling.
-
Simultaneous detection of DNA variants and RNA fusions
In this webinar, we’ll discuss customized solutions for optimized workflows to address specific applications, powered by our Enterprise Genomics Services (EGS). This is a concierge-style approach to project design and management, built upon years of experience in development and rapid integration of custom solutions into the laboratory.
-
Single NGS workflow for DNA and RNA analysis from a single sample
-
Part 1: One-day workflow for simultaneous profiling of DNA variants and RNA fusions
-
Part 2: Curated panels and custom workflows for profiling DNA and RNA biomarkers in parallel
-
Evolution of tumor profiling in a clinical lab
-
Simultaneous detection of DNA variants and RNA fusions
All photos taken prior to COVID-19