Single-Cell, Bulk & Spatial Services Fast, high-quality transcriptomics services
Our team runs your project end to end, from sample strategy and experimental design to sequencing and data analysis, so you can outsource with confidence and focus on the biology.
Trusted by
Transcriptomics services with proven expertise
Built on experience, not just workflows
We provide bulk, single-cell, and spatial transcriptomics services grounded in experience and technical rigor. Our team works as an independent partner to design and execute experiments that deliver reliable data and scale with your research goals.
Discovery-seq
Designed specifically for pharma-grade throughput and decision-making.
- Enhanced Drug-seq alternative with improved sensitivity and robustness
- Optimized for large-scale compound screening and mode-of-action studies
- Lower cost per condition with higher data consistency
10x Genomics
Certfied Service provider of 10x Genomics single-cell and multiome sequencing services enabling transcriptomic, immune, and epigenomic insights at scale.
- Single Cell Gene Expression for robust, large-scale transcriptomic profiling
- Single Cell Immune Profiling linking expression with TCR/BCR clonotypes
- Single Cell Gene Expression Flex for fixed and challenging samples
- ATAC Multiome measuring expression and chromatin accessibility per cell
Visium HD
Whole-transcriptome spatial gene expression profiling at a single-cell resolution.
- High spatial fidelity across entire tissue sections
- Compatible with FFPE, fresh frozen, and fixed samples
- Ideal for tissue microenvironment and spatial biology studies
Split-Pool
Ultra-high-throughput combinatorial barcoding single-cell sequencing services using validated technologies from Parse Biosciences and Scale Biosciences.
- Cost-effective sequencing of hundreds of thousands of cells
- Ideal for large atlases and population-level studies
- Detect lowly-expressed genes and reduce ambient RNA
- Well-suited for fixed samples
Sequencing Service
Fast, high-throughput sequencing services on client-prepared libraries on Illumina platforms with expert support and quality control.
- High-quality sequencing on NovaSeq X Plus
- Fast turnaround times of 2 weeks with flexible delivery options
- Project-specific run configurations and read setups
Data Consulting
In addition to the standard data analysis included with every project, we offer dedicated data consulting to support advanced interpretation and custom analytical needs.
- Custom analysis beyond standard pipelines and reports
- Support for experimental design and statistical strategy
- Deep biological interpretation of complex single-cell datasets
ResolveServices™
Integrated single-cell DNA and RNA sequencing delivered as a certified service provider for BioSkryb Genomics using validated multiomic workflows.
- Simultaneous genome and transcriptome profiling from the same cell
- High-fidelity single-cell whole-genome sequencing
- Direct linkage of genetic variation to gene expression
Proteomics
By integrating transcriptomics with proteomics through our partnerships in high-throughput FFPE proteomics with Sapient and Olink proteomics with TATAA Biocenter, we deliver a more comprehensive, multi-layered understanding of our clients’ research.
- Simultaneous proteomics and transcriptome profiling from the same fixed sample
- Improved biomarker discovery and validation
- Greater pathway and mechanism understanding
Bulk Sequencing
Comprehensive transcriptome profiling of pooled samples using either standard poly(A) bulk RNA-seq or total bulk RNA-seq to capture coding and non-coding RNA expression.
- Choice between poly(A) or total RNA, depending on the biological question
- Ideal for pathway analysis, differential expression, and validation studies
- Compatible with low-input and diverse sample types
SORT-Seq
Sensitive plate-based single-cell RNA sequencing using FACS and 384-well plates, exclusively offered by Single Cell Discoveries.
- Ideal for low cell inputs and rare populations
- High sensitivity and flexible sample compatibility
- Published and widely cited methodology
VASA-seq
Plate-based full-length and total RNA single-cell sequencing to capture complete transcriptomes, including non-coding RNA.
- Captures full transcript length, not just 3’ ends
- Excellent for non-coding RNA and complex transcript structures
- Complements other single-cell approaches for deeper biology
Custom assays
Tailored transcriptomics asssay development with R&D innovations to suit your research question.
- Adaptations of current workflows for unique project needs
- Novel protocols to enhance sensitivity, accuracy, and flexibility
- Custom solutions for challenging tissues or uncommon species
- Deep expertise from our dedicated research and development team
Download Our Services Brochure
Explore our complete portfolio of single-cell, bulk and spatial transcriptomics services, and how they fit your research.
Why choose SCD?
We are the transcriptomics experts
- Developing single-cell technologies since 2012
- Fast turnaround times (under 4 weeks)
- Experts in bulk, single-cell, and spatial transcriptomics
- Experience with low-input and precious samples
- Sequenced 50+ species and tissue types
- Proprietary assays and assay development
Unmatched expertise in single-cell
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.
Technology choices you can trust
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 are your collaborative partner
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.
What our clients say
"SCD performed a single-cell immune and protein profiling analysis using a bespoke panel on a large set of our blood samples, generating a high-quality dataset. They did a fantastic job in performing the wet lab workflow, ensuring minimal batch effects. The team was professional and responsive, actively working with us to optimize the experimental design and kit chemistry to meet our analytical goals. We were impressed by the overall quality."
Duncan McKenzie, Discovery Lead at IMU Biosciences
"The service of Single Cell Discoveries guarantees a smooth process between customer and company. In case of problems or questions, the scientists reacted competently and immediately, so that answers could be found quickly and flexibly."
Prof. Dr. Stella Autenrieth, Research Group Leader at German Cancer Research Center
"Fantastic job made by a really professional and friendly team. I strongly recommend Single Cell Discoveries for sequencing services."
Samuel García Pérez, Principal Investigator at Galicia Sur Health Research Institute
"Every step of the process has been perfect, starting from the initial informative meeting, where I received useful suggestions, to the experimental phase, which was carried out very quickly. Additionally, communication has been prompt and highly effective."
Andrea Ghiroldi, Staff Scientist at Italfarmaco
"I had a great experience working with Single Cell Discoveries. Service was of excellent quality and fast, and I really appreciated your personalized guidance. I would like to highlight how great it was to work with the data team; it was very easy to communicate with them, and they analyzed our challenging data set exactly as we had in mind, always making sure to understand our needs."
Marta Cuenca-Lopera, Assistant Professor at Center for Translational Immunology, UMC Utrecht
Case studies
Pioneering 10x Flex on OCT-Embedded Patient Brain Tissue
10x Genomics opened the gates for single-cell sequencing on non-fresh, non-thawed tissue with their Chromium Single Cell Gene Expression Flex (10x Flex) kit. Now, we have been successful in performing…
Immune Profiling of atherosclerosis reveals new therapeutic potential
A team of scientists uses 10x Genomics Single Cell Immune Profiling to characterize T cells in the atherosclerotic plaque. Their results redefine atherosclerosis as an autoimmune disease.
Mechanism of disease: a new hypothesis for atherosclerosis
To elucidate atherosclerosis’ mechanism of disease, Sheffield University researchers analyzed the transcriptomes of single endothelial cells.
Services Brochure
Discover our single-cell sequencing solutions
Download our complete portfolio of single-cell, bulk, and spatial transcriptomics services, and learn how they fit your research.
Split-Pool
Sequencing Service
Data Consulting
Bulk Sequencing
SORT-Seq
VASA-seq
Custom assays
Unmatched expertise in single-cell
Technology choices you can trust
We are your collaborative partner


