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.

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SCdiscoveries lab
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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.

DRUG-seq

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
Explore our Drug-seq alternative
Single-cell sequencing

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
Explore our 10x Genomics services
Spatial Transcriptomics

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
Explore our Visium HD service
Single-cell sequencing

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

Explore our Parse Bio services

Explore our Scale Bio services
Single-cell sequencing

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
Explore our sequencing service
Data Analysis

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
Explore our data analysis services
Multiomics

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
Explore our ResolveServices
Multiomics

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
Contact us for multiomic projects
Bulk sequencing

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
Explore our bulk sequencing services
Single-cell sequencing

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
Explore our SORT-seq service
Single-cell sequencing

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
Explore our VASA-seq service
R&D

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
Learn about our R&D
High resolution Biology. Transcriptomics Solutions for research and drug development

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Explore our complete portfolio of single-cell, bulk and spatial transcriptomics services, and how they fit your research.

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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
Single cell sequencing Illumina NovaSeq scientist places samples in the new NovaSeq X machine

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.

collaborate iconWe 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

Case studies

Amsterdam UMC

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…

10x
Neuroscience
Neuroscience
RNA Flex

Recent publications

iScience

Tumor-derived colorectal cancer organoids induce a unique Treg cell population by directing CD4+ T cell differentiation

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.