
Overview
Drive novel discoveries in transcriptomics and gene expression research with powerful RNA sequencing (RNA-seq) solutions. Are you working with limited or degraded RNA samples for your RNA-seq applications or struggling to achieve on-target gene expression reads? Empower yourself with high-performance QIAseq RNA-seq solutions to conquer the complexity of the transcriptome – while saving time and effort.
Want to discuss your RNA-seq project?
Our specialists are on hand to answer all your questions and help you find the best solutions for your project.
rRNA removal
Stranded RNA-seq
3’ RNA-seq
miRNA-seq
Single-cell RNA-seq
RNA fusions
Targeted RNA panels
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Automate and accelerate your library prep
How can automating your NGS library prep benefit your lab?
Success stories
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Sequencing COVID-19 mutations after jumping speciesFirst there was a mink-associated COVID-19 strain outbreak. Then several countries reported variants in household pets. But Denmark had a plan to combat these potential vaccine escape mutants.
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Faster cancer diagnoses using Artificial IntelligenceJapanese startup, PFDeNA, uses deep learning to quickly and accurately detect and diagnose different cancer types.
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Attacking cancer from all anglesHow QIAseq FastSelect helps pave the way towards more successful cancer treatment.
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Diabetes linked to arsenicDiscovering the connection between environmental arsenic exposure and type II diabetes with QIAGEN Genomic Services.
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The immune system as medicineImmune cells are manipulated to defend against cancer using QIAGEN’s next-generation sequencing technologies.
Your guide to RNA-seq success with degraded, low-quality or difficult-to-sequence RNA samples
Not getting sufficient on-target reads? Working with limited or fragmented RNA? See why QIAseq RNA-seq technologies are designed to work optimally with the most challenging of samples:
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Maximize on-target reads with efficient rRNA removal
- One-step removal of >95% unwanted rRNA
- Enhances RNA-seq sensitivity
- Rapid, streamlined workflow
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Low-input, gel-free miRNA-seq
- Streamlined, gel-free workflow
- Works with 1 ng total RNA
- Unique molecular indices eliminate bias
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High-throughput 3’ RNA-seq
- Ultraplex (UPX) tagging allows 4608–18,432 samples per single sequencing lane
- Unique molecular indices help eliminate PCR bias
- Locked nucleic acid technology maximizes insights from low-input sampes
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FFPE sample design algorithm
- Specific algorithms around FFPE samples – smaller and denser amplicons
- Optimized products that capture and work with fragmented RNA
- Bioinformatics and chemistry that adjusts for read quality and modified bases
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Discover Genomic Services
Combine unparalleled expertise and support with our high-performance RNA-seq technologies
All photos taken prior to COVID-19