TechnologiesRNA-SeqmRNA-Seq

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.

Resources

Overview of bioanalysis in advanced therapies

  • Assay design and validation
  • Regulatory guidelines (EMA and FDA)
  • Challenges and best practices

Genomic biomarker analysis (DNA, RNA, miRNA, ctDNA etc,)

  • Technology overview
  • Analytical validation
  • Regulatory overview

Capability PDF

Download our latest brochure for a summary of our molecular CRO services and capabilities.

Your trusted partner for mRNA-seq analysis .