Two scientists talking about the results
Genomic Services

RNA Sequencing Services

Targeted approach for profiling low-abundance transcripts

Despite the advantages of next-generation sequencing (NGS), not every lab has the time or resources to take advantage of this technology. QIAGEN Genomic Services overcomes these limitations by combining our innovative QIAseq RNA sequencing technology with decades of technical expertise. QIAseq Targeted RNA Panels include molecular bar code technology and provide two-stage PCR-based library preparation to deliver unbiased and accurate quantification for your targeted RNA sequencing results.

Extend your in-house resources with the expertise and service that you expect from QIAGEN. Our all-in-one Targeted RNA Sequencing Service offers the following benefits:

  • End-to-end service: We take care of every step, from sample preparation to data analysis
  • Guidance and flexibility: We aid in designing your project and targeted panel, and help you make the right decisions
  • Powerful digital sequencing approach: Our optimized QIAseq technology combines unique molecular indices (UMIs) and single primer extension (SPE) to deliver unbiased and accurate quantification
  • Ready-to-publish data: We deliver comprehensive reports and data packages, and provide guidance on the next steps

Partner with us for expert guidance and dedicated service – from Sample to Insight® – to unlock the potential of RNA sequencing in your lab today.

Sample type Purification
RNeasy Plus Kit, miRNeasy Mini/Micro Kit
Tissue: fresh- frozen, stabilized or FFPE
RNeasy Plus Universal Kit, RNeasy FFPE Kit, miRNeasy Mini Kit
PAXgene Blood miRNA Kit

Biofluids: serum, plasma (EDTA and citrate), urine, cell media,
exosomes, buccal swabs, saliva, cerebral spinal fluid, stool

miRNeasy Serum/Plasma Kit, exoRNeasy Serum/Plasma Kit,
miRCURY Exosome Cell/Urine/CS Kit, miRNeasy Micro Kit

Report and final consultation

The final report, delivered by our cloud-solution or on hard drive, provides the following:

  • An easy-to-read data report containing a description of the project, assessments of sample and data quality, as well as an overview of the data analysis results, including publication-grade illustrations
  • A data analysis file which is sufficient for publication, or performing your analysis of the data if desired
  • A materials and methods section, ready to use for publication purposes
  • Complete encrypted raw data (including FASTQ and BAM files when possible)

After you have received your report, we arrange a follow-up discussion to answer any questions you may have about your report and discuss the significance of your results and the next steps. We can also help you design appropriate miRCURY LNA or RT2 qPCR assays to validate your NGS data with us.

Learn more about these RNA Sequencing Services

Contact Genomic Services

Learn more about the options available to you and consult with experts about solutions for your projects.