Discover trends, market shifts, and competitive outlooks for the sanger sequencing industry through 2025-2034 with The Business Research Company’s reliable data and in-depth research

What Is the Estimated Market Size of the Sanger Sequencing Market In 2029?

The market size of Sanger sequencing has witnessed a swift expansion in the last few years. A significant surge from $2.75 billion in 2024 to $3.3 billion in 2025, exhibiting a compound annual growth rate (CAGR) of 19.8%, is anticipated. The dramatic rise in the past era is credited to a surge in research requirements, advancement in medical diagnostics, escalation in pharmaceutical development, expansion in agricultural applications, enhancement in forensic analysis, proliferation in biomarker discovery, and a surge in genetic evolution studies.

Expectations are high for the sanger sequencing market, as it is projected to experience significant growth in the forthcoming years. Forecasts predict the market to expand to a value of $6.17 billion by 2029, representing a compound annual growth rate (CAGR) of 16.9%. This anticipated growth during the forecast period is believed to be propelled by the heightened integration of clinical genomics, the extensive expansion of agricultural genomics, advancements in drug safety and pharmacogenomics, increased prenatal and newborn screenings, and a rise in environmental DNA analysis. Key trends anticipated to shape the market in the forecast period encompass technological developments, surging demand for next-generation sequencing, burgeoning applications in clinical diagnostics, increased funding in genomics research, and an expanding role in personalized medicine.

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Which Major Market Drivers Are Expected to Boost the Growth Potential of the Sanger Sequencing Market?

The surge in genetic diseases is predicted to fuel the expansion of the sanger sequencing market in the future. Genetic diseases, otherwise known as genetic disorders, are health conditions resulting from anomalies or changes in a person’s DNA, which carries hereditary information. Sanger sequencing diagnoses these genetic diseases by identifying the precise sequence of nucleotides, which are the building blocks of DNA, in a particular gene or DNA region. For example, figures from the National Health Service, a publicly funded healthcare system based in the UK, disclosed that around 2,300 individuals in the UK were living with thalassaemia as of August 2024. Of those, approximately 800 suffer from a severe form of the disorder and require regular blood transfusions. Consequently, the growing prevalence of genetic diseases is spurring the sanger sequencing market’s growth.

Which Key Market Segments Comprise the Sanger Sequencing Market and Drive Its Revenue Growth?

The sanger sequencing market covered in this report is segmented –

1) By Sequencing: Shotgun Sequencing, Targeted Gene Sequencing, Other Sequencing

2) By Laboratory: Wet Labs, Dry Labs

3) By Research: In-House, Outsourced

4) By Application: Diagnostics, Biomarkers and Cancer, Reproductive Health, Personalized Medicine, Forensics, Other Applications

5) By End User: Academic, Government Research Institutes, Pharmaceutical Companies, Biotechnology Companies, Hospitals, Clinics

Subsegments:

1) By Shotgun Sequencing: Whole Genome Shotgun Sequencing, Metagenomic Shotgun Sequencing

2) By Targeted Gene Sequencing: Amplicon Sequencing, Exome Sequencing

3) By Other Sequencing: Nested PCR Sequencing, Sequencing By Synthesis (SBS)

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Which Areas Are Leading Regions in the Sanger Sequencing Market Expansion Across the Globe?

North America was the largest region in the sanger sequencing market in 2024. The regions covered in the sanger sequencing market report are Asia-Pacific, Western Europe, Eastern Europe, North America, South America, Middle East, Africa.

What Are the Key Market Trends in theSanger Sequencing Market Over the Coming Years?

Leading firms in the sanger sequencing market like Source Genomics are strategizing growth by extending their genomic labs to Northern UK with the goal of providing fast and efficient Sanger sequencing services. These labs are known for their genetic testing and analysis, which allow for a deeper understanding of genes and genomes, benefiting areas such as disease diagnosis, scientific research, and personalized healthcare. Furthermore, in June 2023, Source Genomics announced plans to expand their genomic lab in the North of UK, an effort that would increase their Sanger sequencing capabilities and reduce data delivery times. This move represents a significant achievement in enhancing nationwide access to genomic services, particularly for research institutions. By extending their reach geographically, they offer customers all over the UK the opportunity to take advantage of superior Sanger sequencing services with faster delivery times.

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How Is the Sanger Sequencing Market Conceptually Defined?

Sanger sequencing, or chain termination sequencing, is a method for determining the nucleotide sequence of DNA. Sanger sequencing is used for smaller-scale initiatives and for validating the outcomes of deep sequencing, as it can create DNA sequence reads of more than 500 nucleotides and maintain accuracy levels.

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