How has the sanger sequencing market evolved, and where is it heading next?
The sanger sequencing market size has grown rapidly in recent years. It will grow from $2.75 billion in 2024 to $3.3 billion in 2025 at a compound annual growth rate (CAGR) of 19.8%. The growth in the historic period can be attributed to increased research demand, increasing medical diagnostics, increased pharmaceutical development, increased agricultural applications, increased forensic analysis, increased biomarker discovery, increased genetic evolution studies.
The sanger sequencing market size is expected to see rapid growth in the next few years. It will grow to $6.17 billion in 2029 at a compound annual growth rate (CAGR) of 16.9%. The growth in the forecast period can be attributed to increasing clinical genomics integration, expanded agricultural genomics, increasing drug safety and pharmacogenomics, increasing prenatal and newborn screening, increasing environmental DNA analysis. Major trends in the forecast period include technological advancements, growing demand for next-generation sequencing, increasing applications in clinical diagnostics, rising investments in genomics research, expanding use in personalized medicine.
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What have been the primary factors driving the sanger sequencing market’s growth?
The rise in genetic illness is expected to propel the growth of the sanger sequencing market going forward. A genetic illness, or genetic disorder, is a medical condition caused by abnormalities or mutations in an individual’s DNA, the hereditary material that carries genetic information. Sanger sequencing is used to diagnose genetic illnesses by determining the exact order of nucleotides (the building blocks of DNA) in a specific gene or region of DNA. For instance, in August 2024, according to the National Health Service, a UK-based publicly funded healthcare system, approximately 2,300 individuals in the UK are living with thalassaemia as of 2024. Among them, around 800 have the severe form of the condition and depend on regular blood transfusions. Therefore, the rise in genetic illness is driving the growth of the sanger sequencing market.
What are the key segments within the sanger sequencing market?
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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Sanger Sequencing Market Opportunities And Analysis Report 2025
Which key players are shaping the sanger sequencing market?
Major companies operating in the sanger sequencing market report are Hoffmann-La Roche, Thermo Fisher Scientific Inc., Merck KGaA, Eurofins Scientific, Illumina Inc., Beckman Coulter, PerkinElmer Inc., BGI Group, LGC Limited, GenScript, Oxford Nanopore Technologies, Pacific Biosciences of California Inc., Macrogen Inc., GENEWIZ Inc., Quintara Biosciences, CeMIA SA, Source BioScience, Microsynth AG, Fasteris SA, GenHunter Corporation, Nucleics Pty. Ltd., SciGenom Labs Pvt. Ltd., StarSEQ GmbH, GATC Biotech AG, Agilent Technologies
How will emerging trends drive the sanger sequencing market throughout the forecast period?
Major companies operating in the sanger sequencing market are focusing on expanding genomic laboratories to provide rapid sanger sequencing services to the North of the UK. Genomic laboratories are specialized facilities that conduct genetic testing and analysis to study the structure, function, and inheritance of genes and genomes, often for purposes such as diagnosis, research, and personalized medicine. For instance, in June 2023, Source Genomics, a UK-based company that offers genomic services, declared the extension of their genomic laboratory into the UK’s north, which will boost the capacity of their Sanger sequencing services and speed up data delivery turnaround times. Expanding laboratory operations to the northern territories is a major advancement in providing equitable access to genomic services for research organizations nationwide. This geographical growth will allow customers across the country to benefit from top-quality Sanger sequencing services with quicker turnaround times.
How do regional factors impact the sanger sequencing market, and which region is the largest contributor?
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 Does The Sanger Sequencing Market Report 2025 Offer?
The sanger sequencing market research report from The Business Research Company offers global market size, growth rate, regional shares, competitor analysis, detailed segments, trends, and opportunities.
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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Sanger Sequencing Market Opportunities And Analysis Report 2025
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