The France Next-Generation Sequencing (NGS) Services Market was valued at $62.7 Million in 2017 and projected to reach to $151.1 Million by 2022, representing a compound annual growth rate of 19.2%. France's NGS services market is poised for sustained growth through 2022 and beyond, driven by increasing healthcare investments in precision medicine and genomic research infrastructure.
| Market Size in | USD 26.32 MN |
| Market Forecast in | |
| CAGR | |
| Forecast Period | |
| Units Considered | Value (USD MN) |
France's NGS services market grew from $62.7 million in 2017 to $151.1 million by 2022, representing a 19.2% CAGR and demonstrating strong adoption of genomic sequencing technologies across the country.
French healthcare institutions are increasingly integrating NGS into clinical diagnostics for cancer genomics, rare disease identification, and personalized medicine, driving demand for specialized sequencing services.
France's robust pharmaceutical and research sectors are leveraging NGS for drug development, biomarker discovery, and clinical trials, positioning the country as a key hub for genomic innovation in Europe.
France's 19.2% CAGR slightly trails the global market's 21% growth rate, indicating competitive positioning while maintaining strong regional momentum in Western European genomics adoption.
| COMPANY | USE CASE DESCRIPTION | BENEFITS |
|---|---|---|
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Commercial NGS services covering clinical whole-genome sequencing, exome sequencing, RNA sequencing, targeted sequencing, 16S microbiome profiling, and metagenomics for clinical research, precision medicine, and microbial studies. | Integrated sequencing and bioinformatics | CAP/CLIA-validated clinical options | Customizable workflows for diverse applications |
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WGS, WES, transcriptome, metagenome, epigenome, and single-cell sequencing services used in disease research, biomarker discovery, precision medicine, population studies, and microbiome analysis. Services include sequencing and downstream bioinformatics. | Broad multi-omics service portfolio | High-throughput sequencing capacity | End-to-end sequencing and data analysis support |
Logos and trademarks shown above are the property of their respective owners. Their use here is for informational and illustrative purposes only.
| Report Metric | Details |
|---|---|
| Base Year | 2017 |
| Fastest Growing Segment | AGRICULTURE & ANIMAL RESEARCH (Application) |
| Forecast Period | 2017–2022 |
| Growth Rate | CAGR of 21% from 2017 to 2022 |
| Largest Segment | DIAGNOSTICS (Application) |
| Market Size Base Year (Billions) | ~USD 1.06 (2017) |
| Revenue Forecast (Billions) | ~USD 2.748 (2022) |
| Segments Covered | Type, Application, End User, Technology |
4 segment dimensions are covered across the global market.
| Company | HQ | Ownership | Strongest segments |
|---|---|---|---|
| ILLUMINA, INC. | United States | Public Company | Targeted sequencing services,RNA-Seq services,Exome sequencing services, |
| PERKINELMER, INC. | United States | Public Company | Targeted sequencing services,RNA-Seq services,Exome sequencing services, |
| EUROFINS SCIENTIFIC SE | Luxembourg | Public Company | Targeted sequencing services,RNA-Seq services,Exome sequencing services, |
| MACROGEN, INC. | South Korea | Public Company | Targeted sequencing services,RNA-Seq services,Exome sequencing services, |
| QIAGEN N.V. | Netherlands | Public Company | Targeted sequencing services (panels, amplicon, gene panels),RNA-Seq services,Exome and de novo sequencing services, |
| DNA LINK, INC. | South Korea | Public Company | Whole genome & De Novo sequencing services,Whole exome & targeted sequencing services,Transcriptome & single-cell RNA sequencing, |
| TAKARA BIO INC. (PART OF TAKARA HOLDING COMPANY INC.) | Japan | ||
| NOVOGENE CORPORATION | China | Public Company | Whole genome and targeted sequencing services (incl. human/animal/plant/microbial WGS and targeted panels),Transcriptomics and single-cell sequencing (mRNA, lncRNA, small RNA, single-cell, spatial),De novo, metagenomics, and microbiome sequencing, |
| PERSONALIS, INC. | United States | Public Company | Oncology MRD and monitoring (NeXT Personal, NeXT Personal Dx),Comprehensive tumor profiling (ImmunoID NeXT, NeXT Dx),Population and research sequencing (WES/WGS services), |
Illumina, Inc. is a public company founded in 1998 and headquartered in the United States with 8,625 employees. The company is a leader in DNA sequencing and genetic analysis technologies.
PerkinElmer, Inc. is a public company founded in 1937 and based in the United States with 11,000 employees. The company provides diagnostic and research solutions across life sciences and environmental testing.
Eurofins Scientific SE is a public company founded in 1987 and headquartered in Luxembourg with 65,694 employees. The company operates a network of laboratories providing testing and analytical services across multiple industries.
Macrogen, Inc. is a public company founded in 2000 and based in South Korea with 293 employees. The company provides genomic research services including DNA sequencing and analysis.
QIAGEN N.V. is a public company founded in 1984 and headquartered in the Netherlands with 5,500 employees. The company develops and manufactures molecular diagnostics and life sciences tools.
DNA Link, Inc. is a public company founded in 2000 and based in South Korea with 84 employees. The company offers genomic analysis and genetic testing services.
Takara Bio Inc. is a company based in Japan and operates as part of Takara Holding Company Inc. The company specializes in biotechnology and life sciences research products.
Novogene Corporation is a public company founded in 2011 and based in China with 2,225 employees. The company provides genomic sequencing and bioinformatics analysis services.
Personalis, Inc. is a public company founded in 2011 and based in the United States with 260 employees. The company develops genomic testing and analysis solutions for precision medicine.
France's NGS Services Market was valued at $62.7 million in 2017, serving as the baseline for market analysis and growth projections.
France's NGS Services Market was forecasted to reach $151.1 million by 2022, reflecting sustained expansion driven by precision medicine adoption.
France's NGS Services Market demonstrated a compound annual growth rate (CAGR) of 19.2% between 2017 and 2022.
France's NGS growth is driven by precision medicine initiatives, government support for genomic research, declining sequencing costs, and regulatory frameworks supporting clinical genomic testing integration.
France's oncology, rare disease diagnosis, and infectious disease monitoring sectors are experiencing the most rapid NGS Services adoption among hospitals, diagnostic laboratories, and research institutions.
This research study extensively utilized secondary sources, directories, and databases to identify and collect valuable information for analyzing the global NGS services market. In-depth interviews were conducted with various primary respondents, including key industry participants, subject-matter experts (SMEs), C-level executives of key market players, and industry consultants, to obtain and verify critical qualitative & quantitative information and assess the growth prospects of the market. The global market size estimated through secondary research was triangulated with primary research inputs to determine the final market size.
Secondary research was primarily used to identify and collect information for the comprehensive technical, market-oriented, and commercial study of the NGS services market. The secondary sources used for this study include Centers for Disease Control and Prevention (CDC), National Human Genome Research Institute (NHGRI), International Chromosome and Genome Society (ICGS), European Society of Human Genetics (ESHG), Centre for Cellular & Molecular Biology (CCMB), European Medicines Agency (EMA), Biotechnology and Biological Sciences Research Council (BBSRC), Organisation for Economic Co-operation and Development (OECD), Population Health Research Institute (PHRI), World Health Organization (WHO), and United States Food & Drug Administration (USFDA). This also includes academic Journals and Company Websites; corporate & regulatory filings, such as annual reports, SEC filings, investor presentations, and financial statements; business magazines & research journals; press releases; and trade, business, and professional associations, among others. Secondary data were collected and analyzed to determine the overall size of the global NGS services market, which was subsequently validated through primary research. These sources were also used to gather key information about major players, market classification, and segmentation based on industry trends, regional/country-level markets, market developments, and technological perspectives.
In-depth interviews were conducted with various primary respondents, including key industry participants, subject-matter experts (SMEs), C-level executives of key market players, and industry consultants, to obtain and verify critical qualitative & quantitative information and assess the market’s prospects. Various primary sources from the supply & demand sides of the market were interviewed to obtain qualitative and quantitative information.

To know about the assumptions considered for the study, download the pdf brochure
In this report, NGS refers to non-Sanger-based, high-throughput DNA and RNA sequencing technologies. NGS is fundamentally based on sequencing by synthesis (SBS), ion semiconductor sequencing, single-molecule real-time (SMRT) sequencing, and nanopore sequencing. The NGS services market encompasses outsourced sequencing and associated laboratory and bioinformatics services provided for comprehensive genomic and transcriptomic analysis. Services include pre-sequencing/sample preparation, library preparation, sequencing, data processing, bioinformatics analysis, and interpretation. The market covers sequencing services such as whole-genome sequencing (WGS), whole-exome sequencing (WES), RNA sequencing, targeted sequencing, and metagenomics/16S sequencing, supporting applications across oncology, infectious disease research, reproductive health, drug discovery, and other life science and clinical research areas.

After evaluating the overall market size through the market size estimation process, the total market was divided into several segments and subsegments. Data triangulation and market breakdown procedures were used, whenever applicable, to complete the overall market engineering process and obtain precise statistics for all segments and subsegments. The data were triangulated by analyzing various factors and trends from the demand and supply sides.
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