mRNA-Seq analysis service
GCLP-compliant, optimized, and automated workflows for mRNA-Seq analysis in drug development, supporting projects from small sample sets to large clinical cohort studies.
mRNA-Seq services at TATAA Biocenter
mRNA-Seq helps quantify and profile active genes by detecting their mRNA transcripts, providing insights into gene expression patterns. Unlike Total RNA-Seq, mRNA-Seq focuses exclusively on coding RNA (mRNA) by enriching for poly(A) RNA.
- Identify differentially expressed genes (DEGs) during drug treatment
- Pathway and gene signature analysis to assess drug response
- Biomarker discovery for predicting drug efficacy and toxicity

mRNA-seq selectively sequences polyadenylated RNA, focusing on messenger RNA (mRNA).
Total RNA-Seq |
mRNA-Seq | 3’-mRNA-Seq | Small RNA-Seq | |
Library preparation | Total RNA-Seq with UMIs and UDIs, including rRNA depletion, and globin depletion for whole blood samples. | mRNA-Seq with UMIs and UDIs, including polyA selection | 3’-mRNA-Seq with UMIs and UDIs | Takara |
Recommended sample input | Whole blood (e.g. PAXgene Blood RNA Tubes) or PBMCs (fresh-frozen or stabilized) Tissue or cells (fresh-frozen or stabilized) FFPE sections from resected tissue or biopsies |
Whole blood (e.g. PAXgene Blood RNA Tubes) or PBMCs (fresh-frozen or stabilized) Tissue or cells (fresh-frozen or stabilized) FFPE sections from resected tissue or biopsies |
Whole blood (e.g. PAXgene Blood RNA Tubes) or PBMCs (fresh-frozen or stabilized) Tissue or cells (fresh-frozen or stabilized) FFPE sections from resected tissue or biopsies |
Whole blood (e.g. PAXgene Blood RNA Tubes) or PBMCs (fresh-frozen or stabilized) Tissue or cells (fresh-frozen or stabilized) Plasma, serum or other biofluids |
Recommended RNA input | Range: 1 ng – 1 ug Standard input: 100ng |
Range: 1 ng – 1 ug Standard input: 100ng |
Range: 1 ng – 1 ug Standard input: 10ng |
Range: 0.1 ng – 1 ug Standard input: 100ng |
Recommended sequencing | Paired-end sequencing PE100, 35M read-pairs per sample or 50M for blood samples | Paired-end sequencing PE100, 25M read-pairs per sample or 40M for blood samples | Single-read sequencing SR50, 5M read-pairs per sample or 10M for blood samples | Single-read sequencing |
Deliverables | Quality-controlled data Fastq files Study report |
Quality-controlled data Fastq files Study report |
Quality-controlled data Fastq files Study report |
Differential gene expression analysis, pathway analysis, custom data analysis (please enquire to discuss further). |
Additional options | Differential gene expression analysis, pathway analysis, cell subset deconvolution, custom data analysis | Differential gene expression analysis, pathway analysis, cell subset deconvolution, custom data analysis | Differential gene expression analysis, pathway analysis, cell subset deconvolution, custom data analysis |
GLP and GCLP compliant laboratory
We are accredited for Good Laboratory Practice (GLP) by the Swedish Board for Accreditation and Conformity Assessment (SWEDAC) for qPCR, dPCR, and molecular biology. In addition, we are Good Clinical Laboratory Practice (GCLP) compliant to ensure the safe and reliable analysis of clinical samples.