Rethink RNA-seq to reveal elusive transcriptomic details

Accelerate genomic surveillance of new SARS-CoV-2 Alpha and Beta variants

SARS-CoV-2 is rapidly mutating. This has ramped up the need for robust, high-throughput NGS technologies for reliable genomic surveillance and phylogeographic tracking. Detect emerging variants with precision with our high-throughput NGS solutions for targeted enrichment and sequencing of the complete SARS-CoV-2 genome.

Overcome RNA-seq data analysis roadblocks

Struggling to make sense of your RNA-seq data? We’ve got just the solution! QIAseq RNA-seq and miRNA-seq kits now include access to the new RNA-seq Analysis Portal – an intuitive, web-based solution made for biologists to simplify data analysis. Fully integrated with GeneGlobe, the RNA-seq Analysis Portal allows you to seamlessly go from generating RNA-seq data to gaining gene expression insights.

Capture unique gene expression reads and maximize RNA-seq success

Is highly abundant ribosomal RNA (rRNA) impacting the sensitivity of your gene expression and transcriptomics research, leading to wasted reads and increased RNA-seq costs? 

Benefit from efficient one-step removal of >95% of unwanted rRNA using QIAseq FastSelect technology. Whether you’re working with mammalian, plant, yeast or bacterial RNA samples, high-quality or degraded or FFPE RNA samples, QIAseq FastSelect can transform your RNA-seq – and outperform Ribo-Zero, RiboErase and RiboMinus.

Elucidate transcriptomic details with high-quality stranded RNA-seq library prep

Want to maximize usable RNA-seq reads, achieve sensitive detection of low-abundance transcripts – and save 44% time with your library prep?

Combine the efficiency of QIAseq FastSelect rRNA removal technology with the strand specificity of QIAseq Stranded RNA Library Kits. Start your RNA-seq workflow with QIAseq FastSelect for one-step removal of >95% rRNA or globin mRNA in just 14 minutes. Then, move onto stranded, high-quality, Illumina-compatible RNA-seq library prep using QIAseq Stranded RNA Library Kits, which work without actinomycin D and dUTP digestion. Analyze stranded RNA-seq data with ease using the integrated RNA-seq Analysis Portal – an intuitive, web-based data analysis solution created for biologists and now included with QIAseq Stranded RNA Library Kits.

Explore high-throughput 3’ RNA-seq for disease and pathway research

The use of 3’ RNA sequencing has been instrumental in unraveling the complexity of cell signaling pathways to reveal a multitude of insights into various diseases. QIAseq UPX 3’ Transcriptome technology provides a high-throughput solution that affords increased accuracy, specificity and sensitivity with limited samples. Apply its multiple benefits in high-throughput screening applications such as toxicology, drug and disease research, single-cell analysis and differential gene expression studies. Analyze 3’ RNA-seq data with ease using the integrated RNA-seq Analysis Portal – an intuitive, web-based data analysis solution created for biologists and now included with QIAseq UPX 3’ Transcriptome Kits.

Deciphering the role of miRNAs in disease research using innovative miRNA-seq technology

miRNA profiling can reveal fascinating insights into a multitude of diseases. However, if you’re working with biofluid samples, low RNA amounts and high inhibitor levels are common issues. Eliminate challenges associated with sample variation and explore differential miRNA expression with a gel-free miRNA-seq solution that’s compatible with just 1 ng total RNA input. Analyze miRNA-seq data with ease and achieve novel disease insights using the integrated RNA-seq Analysis Portal – an intuitive, web-based data analysis solution created for biologists and now included with QIAseq miRNA Library Kits.

Unlock insights into RNA fusions, gene expression and SNVs in a single assay

Get a comprehensive view of important biomarkers by combining RNA fusion detection, gene expression profiling and SNV analysis in a single assay using QIAseq RNA Fusion XP Panels. Achieve superior sensitivity and reduced false positives with the streamlined, low-input workflow. You can even design custom panels to target regions of interest using the easy-to-use custom builder.

Take the digital RNA-seq route for fusion gene and expression analysis

If you’re monitoring gene expression changes or looking to identify fusion genes and variants using targeted RNA-seq, challenges during library construction and NGS analysis lead to sub-optimal results. PCR bias and sequencing artifacts can jeopardize the sensitivity of your data. Our QIAseq panels for RNA-seq applications utilize single primer extension (SPE) and unique molecular index (UMI) technologies for increased precision, accuracy and coverage so you can overcome traditional RNA-seq limitations and reduce bias. With an integrated data analysis pipeline, making the leap from generating RNA-seq data to accumulating insights has never been easier.