Pricing and Service Details
ExpressoSeq – Rapid RNAseq Gene Expression Analysis
ExpressoSeq is our flagship gene expression profiling service, engineered for researchers who need high-resolution data without the wait. By bridging the gap between the simplicity of RT-qPCR and the comprehensive depth of Next-Generation Sequencing, we deliver publication-ready insights with unprecedented turnaround times.
New: ExpressoSeq Eco-light
One of the most cost-effective commercial solutions for pilot studies and high-throughput screens. Evaluate your experimental setup and sample quality early, with the unique flexibility to upgrade sequencing depth on demand.
View Comparison Data
For Research Use Only. Not for use in diagnostic procedures.
| ExpressoSeq Eco-light | ExpressoSeq Core | |
|---|---|---|
| Best For | Pilot studies & High-throughput screens | Standard differential expression studies |
| Price | 49.50 € (Net) | 99.00 € (Net) |
| Depth | 1 Million Reads | 5 Million Reads |
| Library Prep | 3′ mRNA (Oligo-dT) with unique molecular identifiers (UMIs) | |
| Analysis | Standard DGE Analysis with pairwise comparisons | |
| Quality Control | Basic Sample QC | Standard Sample QC |
| Upgrades | 49.50 € to upgrade to core depth | Available upon request |
What You Receive: A Comprehensive Data Package
Your ExpressoSeq results package is delivered via a secure download from cloud-based servers and is designed for immediate use, whether you’re preparing a manuscript, applying for a grant, or planning your next experiment. The package includes:
- Sequencing Report: QC Results and Project Metrics (PDF)
- Data: Raw and Processed Output Files (FASTQ, BAM, and count tables)
- Gene level Results: Differential Gene Expression Analysis (Excel and interactive html page)
- Pathway level Results: Gene set Enrichment Analysis (Excel and visualizations; limited to human and mouse)
- Publication-Quality Figures: Volcano Plots, Heatmaps, Sample Clustering Plots, and more.
- Publication-Ready Description: For your Materials & Methods Section
Technical Specifications
We utilize a streamlined, UMI-powered workflow to ensure every read counts toward your discovery.
- Enrichment: Oligo-dT based mRNA enrichment and reverse transcription
- Sequencing Technology: Oxford Nanopore-based cDNA sequencing of 3′ transcript ends
- Read Lengths: Median read length of ≥300 bases (minimum 80 bases)
- Precision: Unique Molecular Identifiers (UMIs) are used to eliminate PCR duplicates
- Bioinformatics Pipeline: Alignment to reference genome (minimap2); read counting/differential gene expression (Rsubread and edgeR packages in R)