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Single Cell Discoveries

Full company profile

uuid0007srk

Namestring
Single Cell Discoveries
Legal namestring
Single Cell Discoveries BV
Company typeenum
Private
Founded yearint
2018
Descriptiontext

Single Cell Discoveries BV is a privately held Contract Research Organization headquartered in Utrecht, Netherlands, founded in September 2018 by Mauro Muraro (CEO) and Judith Vivié (COO). The company provides end-to-end single-cell and spatial transcriptomics services to pharmaceutical, biotechnology, and academic research customers globally, with disclosed clients including Roche, Pfizer, Almirall, Genmab, DKFZ, Mount Sinai, and Boston Children's Hospital. It operates with 11-50 employees from a laboratory at Utrecht Science Park, with a US sample logistics partnership via MLM Medical Labs in Memphis, TN.

The company's core offering is a technology-agnostic portfolio of single-cell and spatial RNA sequencing services, spanning proprietary plate-based methods (SORT-seq, VASA-seq), third-party platforms (10x Genomics, Parse Biosciences, Scale Bio, BioSkryb), and Illumina NovaSeq X Plus sequencing infrastructure — making it the first holder of that sequencer in the Benelux region. SCD holds Certified Service Provider status with all four major single-cell platform vendors and, in May 2025, became the first laboratory worldwide operationally ready to perform fully automated library preparation for 10x Genomics assays, reducing hands-on time from over five hours to one hour at a throughput of 96 samples per day. Turnaround is four weeks from sample to data for standard projects and two weeks for sequencing-only services.

The business model is professional services revenue on a per-project quote basis following PhD-level scientific consultation, with multi-year contracts common. Marketing is consultative and content-driven rather than transactional, emphasizing the firm's "white-glove" positioning as a scientific thought partner. The company holds a central operational role in the IMI-funded PERSIST-SEQ consortium (with AstraZeneca, Oncode Institute, and others), targeting characterization of 5 million cancer cells over five years, and participates in the Health Holland-funded CLEAR COVID-19 consortium. Pricing is not publicly disclosed; revenue, valuation, and ownership structure beyond founders and a single €50,000 EFRO grant in 2025 are not publicly available.

Short descriptiontext

Single Cell Discoveries is a Utrecht-based CRO providing end-to-end single-cell and spatial transcriptomics services to pharma, biotech, and academic clients using a technology-agnostic platform approach spanning 10x Genomics, Parse, Scale Bio, and proprietary methods.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersUtrecht, Netherlands
HQ citystring
Utrecht
HQ countrystring
Netherlands
HQ regionstring
Europe
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
single-cell sequencing, spatial transcriptomics, bulk RNA sequencing, contract research organization, multiomics services
Industry3 codes
1Single-Cell & Spatial Omics Services
CodeHLAGANACPrimaryYes
2Bioinformatics & Multi-omics Analysis Software
CodeHLAGAJADPrimaryNo
3Bioinformatics, Multi-Omics Data Analysis & Interpretation Services
CodeHLAGANAIPrimaryNo
NAICS code2 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Scientific Research and Development Services5417
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Single-Cell Sequencing Contract Research Services
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model6 records
1Single-Cell Sequencing Services
TypeProfessional Services
Description

Contract research organization providing single-cell and spatial transcriptomics services on a project basis. Services include single-cell RNA sequencing, immune profiling, ATAC-seq, multiomics, plate-based methods (SORT-seq, VASA-seq), and high-throughput options via Parse Biosciences and Scale Biosciences platforms. Revenue generated through per-project pricing with consultation and custom assay development options.

scdiscoveries.com
2Spatial Transcriptomics Services
TypeProfessional Services
Description

10x Genomics Visium HD spatial gene expression services enabling whole transcriptome analysis at single-cell resolution with continuous tissue coverage. Includes sample preparation, library construction, and data analysis.

scdiscoveries.com
3Bulk RNA Sequencing
TypeProfessional Services
Description

Low input, high-quality transcriptome data services including Total Bulk RNA sequencing leveraging Cel-seq2 barcoding. Both normal and low input options available.

scdiscoveries.com
4Sequencing Service
TypeProfessional Services
Description

Standalone sequencing service using Illumina NovaSeq X Plus. Fastest sequencing service in Europe delivering high-quality data in 2 weeks. Accepts ready-to-sequence libraries from clients.

scdiscoveries.com
5Data Analysis Consulting
TypeProfessional Services
Description

Custom data analysis services beyond standard exploratory analysis included with projects. Specialized bioinformatics support, custom pipelines, and integration with third-party tools like BioTuring BBrowserX.

scdiscoveries.com
6Custom Assay Development
TypeProfessional Services
Description

R&D team continuously customizes existing methods to fit unique experimental needs. Proprietary assay development for specific customer requirements.

scdiscoveries.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Personnel, Technology or R&D, Operations, Infrastructure, Supply Chain, Marketing or Sales
Pricing details1 tier
1Project-based CRO services with consultation
ModelOtherBilling cadenceMulti-year contract
Notes

No public pricing available. Services quoted on per-project basis following scientific consultation. Includes standard exploratory data analysis with all projects. Custom analysis available at additional cost. 10% discount mentioned for Scientific Challenge participants who don't win but decide to proceed.

scdiscoveries.com
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 of 3 records shown
1SORT-seq
Description

Plate-based single-cell sequencing service compatible with many sample types and low cell input.

scdiscoveries.com
+2 more records
Core offering1 text field

Single Cell Discoveries is a Contract Research Organization providing end-to-end single-cell and spatial transcriptomics services on a project basis. Offerings span single-cell RNA sequencing (using proprietary SORT-seq and VASA-seq, plus 10x Genomics, Parse Biosciences, and Scale Biosciences platforms), spatial transcriptomics (10x Genomics Visium HD), bulk RNA sequencing, and standalone Illumina NovaSeq X Plus sequencing. Every project includes exploratory data analysis with optional custom bioinformatics consulting.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • Processing capacity increased to 96 samples per day with automated library preparation
+4 more records
Product overview1 text field

Single Cell Discoveries is a Contract Research Organization (CRO) offering a comprehensive portfolio of single-cell and bulk RNA sequencing services. The core offerings include multiple single-cell platforms (SORT-seq plate-based, VASA-seq full-length, 10x Genomics microfluidics, Parse Biosciences scalable, and Scale Biosciences high-throughput), spatial transcriptomics (Visium HD), and bulk RNA sequencing (including Discovery-seq/DRUG-seq for drug discovery). Data analysis is included with all services, with advanced custom bioinformatics available. The company positions itself as a technology-agnostic, scientist-led organization that helps researchers select the right workflow for their specific needs, delivering fully analyzed data within four weeks.

Product and service13 records
1Single-Cell Sequencing
CategorySingle-cell sequencing services
Description

End-to-end single-cell RNA sequencing CRO service using plate-based SORT-seq, Parse Biosciences scalable workflows, and 10x Genomics microfluidics platforms for high-throughput single-cell analysis. Customers include pharma, biotech, and academic research groups needing expert-led experimental design through data analysis.

2SORT-seq
CategorySingle-cell sequencing services
Description

Proprietary plate-based single-cell sequencing service compatible with many sample types and low cell input. Delivered as a CRO service to researchers needing flexible plate-based workflows.

3VASA-seq
CategorySingle-cell sequencing services
Description

Proprietary full-length single-cell RNA sequencing service offering enhanced sensitivity for isoform and splice variant detection. Suitable for complex neural tissues and applications requiring complete transcript characterization. Developed by SCD's Fredrik Salmén.

410x Genomics Single-Cell Services
CategorySingle-cell sequencing services
Description

Certified 10x Genomics service provider offering Single Cell Gene Expression, Single Cell Immune Profiling, Single Cell Gene Expression Flex, Single Cell ATAC-seq, and Epi Multiome workflows with annual recertification.

5Parse Biosciences Single-Cell Services
CategorySingle-cell sequencing services
Description

Certified Parse Biosciences service offering Evercode Single Cell Whole Transcriptome solutions that scale to millions of cells for high-throughput single-cell analysis projects.

6Discovery-seq (DRUG-seq)
CategoryDrug discovery sequencing services
Description

Higher-sensitivity DRUG-seq alternative service providing high-throughput RNA sequencing for drug discovery applications. Enables rapid hit-finding to validation workflow in combination with single-cell sequencing and spatial transcriptomics.

7Bulk RNA Sequencing
CategoryBulk RNA sequencing services
Description

Low input, high-quality transcriptome data service using standard bulk or Total Bulk RNA sequencing with Cel-seq2 barcoding. Available in normal and low input options.

8Visium HD Spatial Transcriptomics
CategorySpatial transcriptomics services
Description

Whole transcriptome spatial gene expression analysis at single-cell resolution with continuous tissue coverage using 10x Genomics Visium HD. Includes sample preparation, library construction, and data analysis.

9BioSkryb Genomics Multi-omic Sequencing Services
CategoryMulti-omic sequencing services
Description

ResolveDNA and ResolveOME multi-omic sequencing services for simultaneous measurement of genomic and transcriptomic information from single cells, delivered as the first European Certified Service Provider of BioSkryb Genomics.

10Sequencing Service (Illumina NovaSeq X Plus)
CategorySequencing services
Description

Standalone sequencing service on Illumina NovaSeq X Plus, described as the fastest sequencing service in Europe delivering high-quality data in 2 weeks. Accepts ready-to-sequence libraries from clients with expert support and flexible data formats.

11Scale Biosciences High-Throughput Sequencing Solutions
CategorySingle-cell sequencing services
Description

High-throughput, cost-effective single-cell sequencing using Scale Biosciences' QuantumScale chemistry with Single Cell Methylation kit and Single Cell CRISPR Guide Enrichment kit, with advanced multiplexing.

12Data Analysis Consulting
CategoryBioinformatics services
Description

Custom bioinformatics and data consulting services beyond the standard exploratory analysis included with all SCD projects. Includes integration with BioTuring BBrowserX for interactive visualization and ImmuneWatch DETECT for TCR epitope prediction from sequencing data.

13Custom Assay Development
CategoryCustom research and development services
Description

Bespoke assay development service where SCD's R&D team customizes existing methods and develops new assays to fit unique experimental requirements for individual customers.

Scale indicator10 records

Each record includes

Type, Value, Description, Source

Partnership12 partners
Strategic tierSupportingTypeOthersAnnounced on2026-05-29
Description

Partnership to streamline sample shipping from the U.S. Domestic shipping address in Memphis, TN enables American clients to send samples more easily with greater reliability.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2025-09-30
Description

Parse Biosciences certified Single Cell Discoveries as a service provider, expanding global access to scalable, high-quality single cell analysis for researchers. SCD offers Parse Biosciences' Evercode Single Cell Whole Transcriptome solutions.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2025-09-10
Description

Partnership to expand TCR single-cell sequencing services by integrating ImmuneWatch's DETECT tool into data consulting services, enabling epitope prediction from TCR sequencing data. Combined with 10x Genomics 5' TCR Immune Profiling for seamless workflow.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2025-05-08
Description

Collaboration since 2023 to automate single-cell gene expression workflows. SCD is the first laboratory trained by both 10x Genomics and Beckman Coulter for fully automated library preparation, enabling 96 samples/day throughput.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2025-03-25
Description

SCD became the first European Certified Service Provider of BioSkryb Genomics' multi-omic sequencing services, offering ResolveDNA and ResolveOME solutions for genomic analysis.

Strategic tierSupportingTypeTechnology or IntegrationAnnounced on2024-09-04
Description

Partnership with Illumina to deliver genome-wide Perturb-Seq experiment using NovaSeq X Plus System, pushing boundaries of functional genomics research.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2023-06-06
Description

First delivery of Illumina NovaSeq X Plus in Benelux. Partnership enables 2.5x greater throughput and reduced sequencing costs. SCD featured in Illumina video highlighting impact on therapy research customers like VectorY.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2023-01-01
Description

Collaboration since 2023 to automate single-cell gene expression workflows. SCD is 10x Genomics certified service provider for Single Cell Gene Expression, Single Cell Immune Profiling, and other 10x solutions.

Strategic tierSupportingTypeTechnology or IntegrationAnnounced on2022-01-19
Description

Collaboration to improve single-cell sequencing research by integrating BioTuring's BBrowserX single-cell data analysis platform. SCD clients receive free access to BBrowserX for data visualization and interactive exploration.

10PERSIST-SEQ Consortium
Strategic tierFlagshipTypeStrategic or Co-development PartnerAnnounced on2021-09-01
Description

Five-year public-private partnership funded by IMI, led by Oncode Institute and AstraZeneca. SCD central role: single-cell library prep, sequencing, and pre-processing for all consortium samples. Goal: characterize 5 million cancer cells to understand drug resistance. Partners include Oncode Institute, Hubrecht Institute, Netherlands Cancer Institute, Wellcome Sanger Institute, and multiple pharma companies.

scdiscoveries.com
Strategic tierCoreTypeTechnology or Integration
Description

SCD is an endorsed provider for Scale Biosciences' Single-Cell RNA and CRISPR Guide Enrichment Kits, offering high-throughput, cost-effective sequencing with advanced multiplexing.

12CLEAR COVID-19 Consortium
Strategic tierSupportingTypeStrategic or Co-development Partner
Description

Public-private partnership funded by Health Holland. SCD contributes single-cell RNA sequencing expertise to assess viral replication and epithelial gene expression in nasal airway cell cultures for COVID-19 drug screening. Partners include UMCU, First Health Pharmaceuticals, QVQ Holding, and Vossensteyn Biomedical.

scdiscoveries.com
Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeOthers
Description

Single-cell isolation and imaging tools provider enabling upstream sample prep workflows that feed into sequencing CROs like SCD. Adjacent ecosystem participant rather than direct competitor.

TypeDirect peer
Description

Global genomics CRO offering single-cell sequencing, spatial transcriptomics, and bulk RNA services with significant European operations. Most direct large-scale peer to SCD's core service model.

TypeDirect peer
Description

Genomics services CRO acquired by Azenta, offering single-cell, next-gen sequencing, and synthesis services to pharma and academic customers globally. Competes for the same enterprise scRNA-seq and spatial transcriptomics projects.

TypeBroad incumbent
Description

World's largest sequencing services provider with full-stack single-cell and spatial omics offerings. Much larger and broader than SCD, but directly competes on cost-sensitive single-cell projects.

TypeBroad incumbent
Description

Diversified European life sciences testing and genomics services business with single-cell and RNA sequencing offerings. Larger and broader portfolio, overlapping on pharma/biotech CRO work.

TypeDirect peer
Description

Genomics CRO offering single-cell sequencing, scATAC-seq, spatial transcriptomics, and bulk RNA services. Mid-sized peer with comparable service catalog and customer base.

TypeEmerging player
Description

Epigenetics-focused services and reagent provider offering single-cell ATAC-seq and multiomics services. Comparable in size and customer type, with overlapping applications in immunology and oncology.

TypeEmerging player
Description

Genomics CRO with single-cell capabilities, particularly strong in immunology and oncology research services. Comparable service catalog with focus on translational research customers.

TypeOthers
Description

Single-cell technology platform vendor whose Evercode kits SCD is certified to run as a service provider. Both technology partner and indirect competitor as Parse expands its own service network.

TypeBroad incumbent
Description

Established single-cell platform vendor (mass cytometry, microfluidics) with services arms. Larger, broader incumbent with overlapping customer base in pharma/biotech translational research.

Market position
Strengths1 record

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Headline, Details, Source

Weaknesses1 record

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Headline, Details, Source

Competitive moat5 records

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Type, Details

Key risks7 records

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Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers12 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment4 records

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Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

Integration3 records

Each record includes

Title, Type, Description, Source

AI capability2 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature5 records

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Title, Differentiator, Description, Source

Core technology
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Profiles10 records

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Name, Designation, Designation category, Overview, Profile commentary, Source

No data
Compliance4 records

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Funding stage, Last funding date, Total funding USD

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Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Single Cell Discoveries

Single-Cell Sequencing Contract Research Servicesscdiscoveries.com

Single Cell Discoveries is a Utrecht-based CRO providing end-to-end single-cell and spatial transcriptomics services to pharma, biotech, and academic clients using a technology-agnostic platform approach spanning 10x Genomics, Parse, Scale Bio, and proprietary methods.

What Single Cell Discoveries does

Single Cell Discoveries BV is a privately held Contract Research Organization headquartered in Utrecht, Netherlands, founded in September 2018 by Mauro Muraro (CEO) and Judith Vivié (COO). The company provides end-to-end single-cell and spatial transcriptomics services to pharmaceutical, biotechnology, and academic research customers globally, with disclosed clients including Roche, Pfizer, Almirall, Genmab, DKFZ, Mount Sinai, and Boston Children's Hospital. It operates with 11-50 employees from a laboratory at Utrecht Science Park, with a US sample logistics partnership via MLM Medical Labs in Memphis, TN.

The company's core offering is a technology-agnostic portfolio of single-cell and spatial RNA sequencing services, spanning proprietary plate-based methods (SORT-seq, VASA-seq), third-party platforms (10x Genomics, Parse Biosciences, Scale Bio, BioSkryb), and Illumina NovaSeq X Plus sequencing infrastructure — making it the first holder of that sequencer in the Benelux region. SCD holds Certified Service Provider status with all four major single-cell platform vendors and, in May 2025, became the first laboratory worldwide operationally ready to perform fully automated library preparation for 10x Genomics assays, reducing hands-on time from over five hours to one hour at a throughput of 96 samples per day. Turnaround is four weeks from sample to data for standard projects and two weeks for sequencing-only services.

The business model is professional services revenue on a per-project quote basis following PhD-level scientific consultation, with multi-year contracts common. Marketing is consultative and content-driven rather than transactional, emphasizing the firm's "white-glove" positioning as a scientific thought partner. The company holds a central operational role in the IMI-funded PERSIST-SEQ consortium (with AstraZeneca, Oncode Institute, and others), targeting characterization of 5 million cancer cells over five years, and participates in the Health Holland-funded CLEAR COVID-19 consortium. Pricing is not publicly disclosed; revenue, valuation, and ownership structure beyond founders and a single €50,000 EFRO grant in 2025 are not publicly available.

Single Cell Discoveries firmographics

Firmographics
Name
Single Cell Discoveries
Legal name
Single Cell Discoveries BV
Website
https://scdiscoveries.com
Company type
Private
Founded year
2018
Operating status
Operating
Headcount range
11–50 employees
Short description
Single Cell Discoveries is a Utrecht-based CRO providing end-to-end single-cell and spatial transcriptomics services to pharma, biotech, and academic clients using a technology-agnostic platform approach spanning 10x Genomics, Parse, Scale Bio, and proprietary methods.
Ownership category
akta.pro rank

Single Cell Discoveries industry classification

Industry
Product category
Single-Cell Sequencing Contract Research Services
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Scientific Research and Development Services (5417)
SIC
Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Single-Cell & Spatial Omics Services (HLAGANAC)
akta.pro secondary industries
Bioinformatics & Multi-omics Analysis Software (HLAGAJAD), Bioinformatics, Multi-Omics Data Analysis & Interpretation Services (HLAGANAI)

Keywords

  • Single-cell sequencing
  • Spatial transcriptomics
  • Bulk RNA sequencing
  • Contract research organization
  • Multiomics services

Where Single Cell Discoveries is headquartered

Location

Headquarters

HQ city
Utrecht
HQ country
Netherlands
HQ region
Europe

Offices2 records

Markets served

Single Cell Discoveries business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Technology or R&D, Operations, Infrastructure, Supply Chain, Marketing or Sales

Revenue model

  1. Single-Cell Sequencing Services: Contract research organization providing single-cell and spatial transcriptomics services on a project basis. Services include single-cell RNA sequencing, immune profiling, ATAC-seq, multiomics, plate-based methods (SORT-seq, VASA-seq), and high-throughput options via Parse Biosciences and Scale Biosciences platforms. Revenue generated through per-project pricing with consultation and custom assay development options.
  2. Spatial Transcriptomics Services: 10x Genomics Visium HD spatial gene expression services enabling whole transcriptome analysis at single-cell resolution with continuous tissue coverage. Includes sample preparation, library construction, and data analysis.
  3. Bulk RNA Sequencing: Low input, high-quality transcriptome data services including Total Bulk RNA sequencing leveraging Cel-seq2 barcoding. Both normal and low input options available.
  4. Sequencing Service: Standalone sequencing service using Illumina NovaSeq X Plus. Fastest sequencing service in Europe delivering high-quality data in 2 weeks. Accepts ready-to-sequence libraries from clients.
  5. Data Analysis Consulting: Custom data analysis services beyond standard exploratory analysis included with projects. Specialized bioinformatics support, custom pipelines, and integration with third-party tools like BioTuring BBrowserX.
  6. Custom Assay Development: R&D team continuously customizes existing methods to fit unique experimental needs. Proprietary assay development for specific customer requirements.

Pricing tiers

ModelBillingPrice
OtherMulti-year contractProject-based CRO services with consultation

Go-to-market motion1 record

Distribution channels3 records

Marketing channels6 records

Single Cell Discoveries product offering

Product offering

Core offering

Single Cell Discoveries is a Contract Research Organization providing end-to-end single-cell and spatial transcriptomics services on a project basis. Offerings span single-cell RNA sequencing (using proprietary SORT-seq and VASA-seq, plus 10x Genomics, Parse Biosciences, and Scale Biosciences platforms), spatial transcriptomics (10x Genomics Visium HD), bulk RNA sequencing, and standalone Illumina NovaSeq X Plus sequencing. Every project includes exploratory data analysis with optional custom bioinformatics consulting.

Product overview

Single Cell Discoveries is a Contract Research Organization (CRO) offering a comprehensive portfolio of single-cell and bulk RNA sequencing services. The core offerings include multiple single-cell platforms (SORT-seq plate-based, VASA-seq full-length, 10x Genomics microfluidics, Parse Biosciences scalable, and Scale Biosciences high-throughput), spatial transcriptomics (Visium HD), and bulk RNA sequencing (including Discovery-seq/DRUG-seq for drug discovery). Data analysis is included with all services, with advanced custom bioinformatics available. The company positions itself as a technology-agnostic, scientist-led organization that helps researchers select the right workflow for their specific needs, delivering fully analyzed data within four weeks.

Differentiator

Problem solved

Functional benefit

Brands

  • SORT-seq: Plate-based single-cell sequencing service compatible with many sample types and low cell input.
  • VASA-seq
  • Discovery-seq

Products and services

  • Single-Cell Sequencing End-to-end single-cell RNA sequencing CRO service using plate-based SORT-seq, Parse Biosciences scalable workflows, and 10x Genomics microfluidics platforms for high-throughput single-cell analysis. Customers include pharma, biotech, and academic research groups needing expert-led experimental design through data analysis.
  • SORT-seq Proprietary plate-based single-cell sequencing service compatible with many sample types and low cell input. Delivered as a CRO service to researchers needing flexible plate-based workflows.
  • VASA-seq Proprietary full-length single-cell RNA sequencing service offering enhanced sensitivity for isoform and splice variant detection. Suitable for complex neural tissues and applications requiring complete transcript characterization. Developed by SCD's Fredrik Salmén.
  • 10x Genomics Single-Cell Services Certified 10x Genomics service provider offering Single Cell Gene Expression, Single Cell Immune Profiling, Single Cell Gene Expression Flex, Single Cell ATAC-seq, and Epi Multiome workflows with annual recertification.
  • Parse Biosciences Single-Cell Services Certified Parse Biosciences service offering Evercode Single Cell Whole Transcriptome solutions that scale to millions of cells for high-throughput single-cell analysis projects.
  • Discovery-seq (DRUG-seq) Higher-sensitivity DRUG-seq alternative service providing high-throughput RNA sequencing for drug discovery applications. Enables rapid hit-finding to validation workflow in combination with single-cell sequencing and spatial transcriptomics.
  • Bulk RNA Sequencing Low input, high-quality transcriptome data service using standard bulk or Total Bulk RNA sequencing with Cel-seq2 barcoding. Available in normal and low input options.
  • Visium HD Spatial Transcriptomics Whole transcriptome spatial gene expression analysis at single-cell resolution with continuous tissue coverage using 10x Genomics Visium HD. Includes sample preparation, library construction, and data analysis.
  • BioSkryb Genomics Multi-omic Sequencing Services ResolveDNA and ResolveOME multi-omic sequencing services for simultaneous measurement of genomic and transcriptomic information from single cells, delivered as the first European Certified Service Provider of BioSkryb Genomics.
  • Sequencing Service (Illumina NovaSeq X Plus) Standalone sequencing service on Illumina NovaSeq X Plus, described as the fastest sequencing service in Europe delivering high-quality data in 2 weeks. Accepts ready-to-sequence libraries from clients with expert support and flexible data formats.
  • Scale Biosciences High-Throughput Sequencing Solutions High-throughput, cost-effective single-cell sequencing using Scale Biosciences' QuantumScale chemistry with Single Cell Methylation kit and Single Cell CRISPR Guide Enrichment kit, with advanced multiplexing.
  • Data Analysis Consulting Custom bioinformatics and data consulting services beyond the standard exploratory analysis included with all SCD projects. Includes integration with BioTuring BBrowserX for interactive visualization and ImmuneWatch DETECT for TCR epitope prediction from sequencing data.
  • Custom Assay Development Bespoke assay development service where SCD's R&D team customizes existing methods and develops new assays to fit unique experimental requirements for individual customers.

Quantifiable outcome

  • Processing capacity increased to 96 samples per day with automated library preparation
  • +4 more outcomes

Companies that use Single Cell Discoveries

Customer profile

Named customers12 records

Segments4 records

Ideal customer profiles2 records

Single Cell Discoveries technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Integration3 records

AI capability2 records

Feature5 records

Single Cell Discoveries partnerships and signals

Strategic signal

Partnerships

Twelve partnerships are on record, tiered supporting, core and flagship.

  • MLM Medical LabssupportingOthers · 29 May 2026Partnership to streamline sample shipping from the U.S. Domestic shipping address in Memphis, TN enables American clients to send samples more easily with greater reliability.
  • Parse BiosciencescoreTechnology or Integration · 30 September 2025Parse Biosciences certified Single Cell Discoveries as a service provider, expanding global access to scalable, high-quality single cell analysis for researchers. SCD offers Parse Biosciences' Evercode Single Cell Whole Transcriptome solutions.
  • ImmuneWatchcoreTechnology or Integration · 10 September 2025Partnership to expand TCR single-cell sequencing services by integrating ImmuneWatch's DETECT tool into data consulting services, enabling epitope prediction from TCR sequencing data. Combined with 10x Genomics 5' TCR Immune Profiling for seamless workflow.
  • Beckman Coulter Life SciencescoreTechnology or Integration · 8 May 2025Collaboration since 2023 to automate single-cell gene expression workflows. SCD is the first laboratory trained by both 10x Genomics and Beckman Coulter for fully automated library preparation, enabling 96 samples/day throughput.
  • BioSkryb GenomicscoreTechnology or Integration · 25 March 2025SCD became the first European Certified Service Provider of BioSkryb Genomics' multi-omic sequencing services, offering ResolveDNA and ResolveOME solutions for genomic analysis.
  • Illumina (Genome-wide Perturb-Seq)supportingTechnology or Integration · 4 September 2024Partnership with Illumina to deliver genome-wide Perturb-Seq experiment using NovaSeq X Plus System, pushing boundaries of functional genomics research.
  • IlluminacoreTechnology or Integration · 6 June 2023First delivery of Illumina NovaSeq X Plus in Benelux. Partnership enables 2.5x greater throughput and reduced sequencing costs. SCD featured in Illumina video highlighting impact on therapy research customers like VectorY.
  • 10x GenomicscoreTechnology or Integration · 1 January 2023Collaboration since 2023 to automate single-cell gene expression workflows. SCD is 10x Genomics certified service provider for Single Cell Gene Expression, Single Cell Immune Profiling, and other 10x solutions.
  • BioTuringsupportingTechnology or Integration · 19 January 2022Collaboration to improve single-cell sequencing research by integrating BioTuring's BBrowserX single-cell data analysis platform. SCD clients receive free access to BBrowserX for data visualization and interactive exploration.
  • PERSIST-SEQ ConsortiumflagshipStrategic or Co-development Partner · 1 September 2021Five-year public-private partnership funded by IMI, led by Oncode Institute and AstraZeneca. SCD central role: single-cell library prep, sequencing, and pre-processing for all consortium samples. Goal: characterize 5 million cancer cells to understand drug resistance. Partners include Oncode Institute, Hubrecht Institute, Netherlands Cancer Institute, Wellcome Sanger Institute, and multiple pharma companies.
  • Scale BiosciencescoreTechnology or IntegrationSCD is an endorsed provider for Scale Biosciences' Single-Cell RNA and CRISPR Guide Enrichment Kits, offering high-throughput, cost-effective sequencing with advanced multiplexing.
  • CLEAR COVID-19 ConsortiumsupportingStrategic or Co-development PartnerPublic-private partnership funded by Health Holland. SCD contributes single-cell RNA sequencing expertise to assess viral replication and epithelial gene expression in nasal airway cell cultures for COVID-19 drug screening. Partners include UMCU, First Health Pharmaceuticals, QVQ Holding, and Vossensteyn Biomedical.

Scale indicators10 records

Recent moves8 records

Expansion highlights6 records

Single Cell Discoveries competitors and assessment

Company assessment

Others

  • Cell Microsystems: Single-cell isolation and imaging tools provider enabling upstream sample prep workflows that feed into sequencing CROs like SCD. Adjacent ecosystem participant rather than direct competitor.
  • Parse Biosciences: Single-cell technology platform vendor whose Evercode kits SCD is certified to run as a service provider. Both technology partner and indirect competitor as Parse expands its own service network.

Direct peers

  • Novogene Corporation: Global genomics CRO offering single-cell sequencing, spatial transcriptomics, and bulk RNA services with significant European operations. Most direct large-scale peer to SCD's core service model.
  • GENEWIZ (Azenta Life Sciences): Genomics services CRO acquired by Azenta, offering single-cell, next-gen sequencing, and synthesis services to pharma and academic customers globally. Competes for the same enterprise scRNA-seq and spatial transcriptomics projects.
  • CD Genomics: Genomics CRO offering single-cell sequencing, scATAC-seq, spatial transcriptomics, and bulk RNA services. Mid-sized peer with comparable service catalog and customer base.

Broad incumbents

  • BGI Group: World's largest sequencing services provider with full-stack single-cell and spatial omics offerings. Much larger and broader than SCD, but directly competes on cost-sensitive single-cell projects.
  • Eurofins Genomics: Diversified European life sciences testing and genomics services business with single-cell and RNA sequencing offerings. Larger and broader portfolio, overlapping on pharma/biotech CRO work.
  • Standard BioTools (formerly Fluidigm): Established single-cell platform vendor (mass cytometry, microfluidics) with services arms. Larger, broader incumbent with overlapping customer base in pharma/biotech translational research.

Emerging players

  • Active Motif: Epigenetics-focused services and reagent provider offering single-cell ATAC-seq and multiomics services. Comparable in size and customer type, with overlapping applications in immunology and oncology.
  • MedGenome: Genomics CRO with single-cell capabilities, particularly strong in immunology and oncology research services. Comparable service catalog with focus on translational research customers.

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Weaknesses1 record

Competitive moat5 records

Key risks7 records

Key highlights7 records

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Frequently asked questions about Single Cell Discoveries

What does Single Cell Discoveries do?

Single Cell Discoveries is a Contract Research Organization providing end-to-end single-cell and spatial transcriptomics services on a project basis. Offerings span single-cell RNA sequencing (using proprietary SORT-seq and VASA-seq, plus 10x Genomics, Parse Biosciences, and Scale Biosciences platforms), spatial transcriptomics (10x Genomics Visium HD), bulk RNA sequencing, and standalone Illumina NovaSeq X Plus sequencing. Every project includes exploratory data analysis with optional custom bioinformatics consulting.

Is Single Cell Discoveries a public or private company?

Single Cell Discoveries is a private company. It is classified as founder individual operated bootstrapped and is currently operating.

When was Single Cell Discoveries founded?

Single Cell Discoveries was founded in 2018. It employs 11 to 50 people.

Where is Single Cell Discoveries based?

Single Cell Discoveries is headquartered in Utrecht, Netherlands, in the Europe region.

How does Single Cell Discoveries make money?

Six revenue lines are on record. Single-Cell Sequencing Services are the primary driver. The others are spatial Transcriptomics Services, bulk RNA Sequencing, sequencing Service, data Analysis Consulting and custom Assay Development.

Who are Single Cell Discoveries's main competitors?

Others on record are Cell Microsystems and Parse Biosciences. Direct peers are Novogene Corporation, GENEWIZ (Azenta Life Sciences) and CD Genomics. Broad incumbents are BGI Group, Eurofins Genomics and Standard BioTools (formerly Fluidigm). Emerging players are Active Motif and MedGenome.

Does Single Cell Discoveries have an API?

No public API is recorded for Single Cell Discoveries.

What industry is Single Cell Discoveries in?

Single Cell Discoveries's product category is Single-Cell Sequencing Contract Research Services. Its primary akta.pro industry code is HLAGANAC, Single-Cell & Spatial Omics Services, with a secondary code of HLAGAJAD, Bioinformatics & Multi-omics Analysis Software. Its NAICS code is 541714 and its SIC code is 8731.

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Live signals
Pharmaceutical TechnologyAdvancing single-cell transcriptomics into the mainstream of biomedical researchBeckman Coulter Life Sciences and 10x Genomics have been collaborating since 2023 to automate single-cell gene expression workflows, enabling researchers to overcome the limitations of traditional manual processes that restricted throughput to 24 samples per day. The collaboration with contract research organisation Single Cell Discoveries (SCD) B.V. has demonstrated that automation can increase processing capacity to 96 samples per day while reducing hands-on time from over five hours to one hour and improving data consistency. Industry experts suggest this technology is following a similar trajectory to next-generation sequencing, moving from specialised labs toward mainstream adoption in biomedical research.PR NewswireSingle Cell Discoveries receives first Illumina NovaSeq X Plus in the BeneluxSingle Cell Discoveries, a contract research organization specializing in single-cell sequencing, announced the receipt of the first Illumina NovaSeq X Plus sequencing system in the Benelux region on June 7, 2023. The NovaSeq X Plus platform can generate more than 20,000 whole genomes per year at $200 per genome, delivering 2.5x greater throughput while reducing sequencing costs. CEO Mauro Muraro stated the investment underscores the company's commitment to providing clients with advanced tools for faster turnaround times and high-quality single-cell workflows.ScdiscoveriesSingle Cell Sequencing CROSingle Cell Discoveries is a transcriptomics CRO that provides single-cell, bulk, and spatial RNA sequencing services with a turnaround time of under four weeks. The company highlights its technology-agnostic approach, proprietary assay development, and experience across 50+ species to support research in immuno-oncology, CNS disorders, and cell & gene therapy.PR NewswireSingle Cell Discoveries joins consortium to build a single-cell cancer atlas to find therapy resistant tumor cellsSingle Cell Discoveries has joined PERSIST-SEQ, a new five-year public-private consortium funded by the Innovative Medicines Initiative and co-led by the Oncode Institute and AstraZeneca, to develop standardized single-cell sequencing workflows for studying cancer drug resistance. The consortium aims to sequence 5 million single cells over five years, with Single Cell Discoveries handling all experimental and bioinformatics workflows at its facility and creating a centralized data portal for open-access sharing. The initiative seeks to address the fact that 90% of the 9.6 million annual cancer deaths result from treatment resistance, which currently lacks comprehensive mechanistic understanding and reliable predictive tools.