
Single Cell Discoveries
We are the only transcriptomics service provider built to deliver high-quality data quickly and reliably. We are scientist-led and technology-agnostic. Our team identifies the right workflow for your research and runs single-cell, bulk, spatial RNA sequencing or bespoke projects from RNA sample to bioinformatic analysis. You receive your results within two to four weeks.
We are the transcriptomics experts
We have worked with single-cell since the early days, across multiple technology generations. Across 50+ organisms and 30+ tissue types, we’ve seen how workflows behave in real biological edge cases. That experience helps us anticipate risks early and deliver decision-ready data.
We continuously evaluate new platforms through internal R&D and real-world validation. We adopt technologies only when they clearly improve data quality, robustness, or interpretability. When commercial options fall short, we build and validate proprietary assays and workflows.
We act as a thought partner, not just a service provider. We help shape experimental design, make trade-offs explicit, and align work with downstream objectives. This approach supports complex, multi-phase programs where confidence and consistency matter.
Our services include:
- Single Cell workflows:
- SORT-seq
- VASA-seq
- 10x Genomics: all solutions
- Parse Biosciences solutions
- Bulk RNA-seq:
- mRNA bulk RNA-seq
- Total bulk RNA-seq
- Discovery-seq: high throughput bulk RNA-seq
- Multiomics:
- 10x Genomics Multiome
- BioSkryb Genomics’ ResolveServices™
- High-throughput FFPE Proteomics
- Olink proteomics
Let’s connect!
General InquiriesMonika Klodawskasales@scdiscoveries.com+31 (0)85 114 60 00
Visiting address:Varrolaan 1003584 BW UtrechtFacility features:
• Experts in bulk, single-cell, and spatial transcriptomics
• Experience with low-input samples
• Sequenced 50+ species and tissue types
• Proprietary assays and assay development