Overview and Scope
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.
Sizing and Forecast
The sanger sequencing market size has grown rapidly in recent years. It will
grow from $2.29 billion in 2023 to $2.75 billion in 2024 at a compound annual
growth rate (CAGR) of 19.9%. 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.
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Segmentation & Regional Insights
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
North America was the largest region in the sanger sequencing market in 2023.
The regions covered in the sanger sequencing market report are Asia-Pacific,
Western Europe, Eastern Europe, North America, South America, Middle East,
Africa.
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Major Driver Impacting Market 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 February 2024, according to the Genetic Rare Diseases
Information Center (GARD, a US-based government agency, there were about 7,000
known rare genetic diseases, accounting for about 1 in 10 people, or 30 million
people in the United States during 2020-2021. Therefore, the rise in genetic
illness is driving the growth of the sanger sequencing market.
Key Industry Players
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
The sanger sequencing market report table of contents includes:
1. Executive Summary
2. Sanger Sequencing Market
Characteristics
3. Sanger Sequencing Market
Trends And Strategies
4. Sanger Sequencing Market
- Macro Economic Scenario
5. Global Sanger Sequencing
Market Size and Growth
.
32. Global Sanger Sequencing Market Competitive Benchmarking
33. Global Sanger Sequencing
Market Competitive Dashboard
34. Key Mergers And
Acquisitions In The Sanger Sequencing Market
35. Sanger Sequencing Market
Future Outlook and Potential Analysis
36. Appendix
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