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市場調查報告書
商品編碼
1916511
全球DNA定序市場:市場規模、佔有率、成長率、產業分析、按類型、應用和地區劃分的分析及預測(2026-2034)DNA Sequencing Market Size, Share, Growth and Global Industry Analysis By Type & Application, Regional Insights and Forecast to 2026-2034 |
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全球DNA定序市場是現代基因組學的關鍵基礎,能夠精確識別核酸序列,用於疾病診斷、藥物研發、個人化醫療、法醫學和演化研究。 DNA定序技術已從第一代桑格定序發展到下一代定序(NGS)和先進的第三代定序(TGS)平台,這些平台具有高通量、長讀長和高精度等優勢。這些進步拓展了定序的應用範圍,包括臨床診斷、腫瘤學、罕見疾病檢測和群體基因體學研究。
DNA定序市場規模及價值
根據市場報告顯示,2025年全球DNA定序市場規模為123.1億美元。預計到2026年,在診斷和實驗室中測序技術日益普及的推動下,該市場規模將增長至133.6億美元。在預測期內,預計到2034年,該市場規模將達到272.5億美元,反映了定序技術快速融入常規臨床工作流程和藥物研發流程。預計2026年至2034年,該市場將以9.32%的複合年增長率成長,這主要得益於技術創新、監管批准以及基因組數據臨床應用價值的不斷提升。
推動市場成長的因素
全基因組定序(WGS)在臨床診斷中的日益普及是推動市場成長的關鍵因素。全基因組定序 (WGS) 能夠全面檢測傳統方法難以發現的基因突變,從而支持早期診斷和標靶治療的選擇。隨著遺傳性疾病和癌症發生率的上升,人們越來越依賴基因組分析進行治療方案製定。
定序資料在藥物發現和生物標記識別的應用日益廣泛,進一步推動了市場需求。製藥公司越來越依賴基因組數據集進行患者分層、臨床試驗優化和治療標靶識別。公共和私人對基因組基礎設施、國家基因組圖譜規劃以及對基於二代測序 (NGS) 的診斷技術的監管支持的投資,正在加速其在臨床實踐中的應用。
市場限制因素與挑戰
一個關鍵的限制因素是全球基因組學和生物資訊學領域熟練專家的短缺。解讀定序資料需要專門的計算技能,這限制了其在資源有限的醫療保健系統中的應用。定序錯誤、假陽性以及重複基因組區域檢測不足等技術挑戰也會影響診斷的可靠性。
基因組資訊高度敏感,因此資料安全和隱私問題仍然是重大挑戰。缺乏標準化的全球基因組數據處理和跨境研究合作監管框架,進一步阻礙了市場擴張,尤其是在新興經濟體。
市場趨勢與技術進步
第三代定序平台發展勢頭強勁,這得益於其生成長讀長的能力,從而能夠準確檢測結構突變和表觀遺傳修飾。奈米孔定序和單分子即時定序技術正越來越多地應用於癌症研究、罕見疾病診斷和微生物組分析。
將人工智慧 (AI) 和機器學習應用於資料解讀正成為一大趨勢,幫助實驗室更有效率地分析大量資料集。基於雲端的生物資訊平台也在改善研究機構間的資料儲存、存取和協作。
液體活檢測序透過檢測循環腫瘤DNA實現非侵入性癌症監測,有助於早期發現並改善治療追蹤。
依產品/服務劃分的市場區隔
依產品/服務劃分,市場分為產品與軟體/服務兩部分。產品部分主要受定序儀、流動池和試劑盒的高需求驅動,預計2026年將佔據63.29%的市場。由於定序工作流程的重複採購週期,耗材預計將快速成長。
軟體/服務部分呈現顯著成長,這主要得益於定序服務外包的增加,尤其是在臨床和藥物研究領域,以及對生物資訊解決方案日益增長的需求。
The global DNA sequencing market is a fundamental pillar of modern genomics, enabling precise identification of nucleotide sequences for disease diagnosis, drug development, personalized medicine, forensic science, and evolutionary research. DNA sequencing technologies have transitioned from first-generation Sanger sequencing to high-throughput Next-Generation Sequencing (NGS) and advanced Third-Generation Sequencing (TGS) platforms, offering rapid processing, long-read capabilities, and enhanced accuracy. These advancements have expanded sequencing applications across clinical diagnostics, oncology, rare disease detection, and population-scale genomics initiatives.
DNA Sequencing Market Size and Market Value
As per the market report, the global DNA sequencing market size was valued at USD 12.31 billion in 2025. The market is projected to grow to USD 13.36 billion in 2026, supported by rising adoption of sequencing technologies in diagnostics and research laboratories. Over the forecast period, the market is expected to reach a market value of USD 27.25 billion by 2034, reflecting rapid integration of sequencing into routine clinical workflows and pharmaceutical research pipelines. The market is projected to expand at a CAGR of 9.32% from 2026 to 2034, driven by technological innovation, regulatory approvals, and expanding clinical utility of genomic data.
Market Drivers Supporting Growth
The growing adoption of Whole Genome Sequencing (WGS) in clinical diagnostics is a major growth driver. WGS enables comprehensive detection of genetic variations that traditional methods often fail to identify, supporting early diagnosis and targeted therapy selection. Rising prevalence of genetic disorders and cancer is increasing reliance on genomic profiling for treatment planning.
Expanding use of sequencing data in drug discovery and biomarker identification is further driving demand. Pharmaceutical companies increasingly rely on genomic datasets for patient stratification, clinical trial optimization, and identification of therapeutic targets. Public and private investments in genomics infrastructure, national genome mapping programs, and regulatory support for NGS-based diagnostics are accelerating clinical integration.
Market Restraints and Challenges
A major restraint is the global shortage of skilled professionals in genomics and bioinformatics. Interpreting sequencing data requires specialized computational expertise, limiting adoption in resource-constrained healthcare systems. Technical challenges such as sequencing errors, false positives, and limitations in detecting repetitive genomic regions also affect diagnostic reliability.
Data security and privacy concerns remain critical, as genomic information is highly sensitive. Lack of standardized global regulatory frameworks for genomic data handling and cross-border research collaborations further complicates market expansion, especially in emerging economies.
Market Trends and Technological Advancements
Third-Generation Sequencing platforms are gaining strong momentum due to their ability to generate long reads, enabling accurate detection of structural variants and epigenetic modifications. Nanopore and Single-Molecule Real-Time sequencing are increasingly adopted in cancer research, rare disease diagnostics, and microbiome analysis.
Integration of artificial intelligence and machine learning in data interpretation is becoming a major trend, helping laboratories analyze massive datasets more efficiently. Cloud-based bioinformatics platforms are also improving data storage, accessibility, and collaboration across research institutions.
Liquid biopsy sequencing is gaining traction for non-invasive cancer monitoring by detecting circulating tumor DNA, improving early detection and treatment monitoring.
Segmentation Analysis by Products and Services
By products and services, the market is divided into products and software & services. The products segment dominated the market with a 63.29% share in 2026, driven by high demand for sequencing instruments, flow cells, and reagent kits. Consumables are expected to grow rapidly due to repeat purchase cycles associated with sequencing workflows.
The software and services segment is witnessing strong growth due to increasing outsourcing of sequencing services and demand for bioinformatics solutions, particularly in clinical and pharmaceutical research settings.
Segmentation by Technique and Type
By technique, Next-Generation Sequencing held the largest market share and is projected to capture 85.99% share in 2026, driven by its cost efficiency, scalability, and compatibility with multiple clinical applications. Third-Generation Sequencing is growing at the fastest pace due to long-read sequencing advantages, while Sanger sequencing remains relevant for validation and small-scale research.
By type, targeted sequencing dominated in 2024 due to its widespread use in oncology diagnostics. Whole genome and whole exome sequencing is expanding rapidly, with an estimated 45.98% market share in 2026, driven by rare disease diagnostics and population genomics studies. Epigenomics is growing rapidly due to rising cancer research applications.
Segmentation by Application and End User
By application, diagnostics leads the market, supported by growing cancer screening programs and genetic disorder testing. Drug discovery and development represents the second-largest segment, driven by genomics-guided clinical trials and biomarker research.
By end user, diagnostic centers dominate due to increasing adoption of NGS in oncology and prenatal screening. Academic and research institutes remain strong contributors through large-scale genome projects, while biotechnology and pharmaceutical companies continue expanding internal sequencing capabilities.
North America dominated the DNA sequencing market with USD 5.74 billion in 2025 and USD 6.21 billion in 2026, supported by advanced research infrastructure, strong reimbursement systems, and large multi-omics programs. The U.S. remains the largest national market due to extensive clinical sequencing adoption and biotechnology investments.
Europe follows with strong government funding, national genome initiatives, and rising cancer prevalence. Asia Pacific is the fastest-growing region due to expanding healthcare investments, government genomics programs, and domestic manufacturing partnerships in China, Japan, and India. Latin America and the Middle East & Africa are witnessing gradual growth supported by expanding diagnostic infrastructure.
Competitive Landscape
Major companies operating in the DNA sequencing market include Illumina, Thermo Fisher Scientific, Oxford Nanopore Technologies, PacBio, QIAGEN, PerkinElmer, Azenta, and BGI Genomics. These players focus on new platform launches, bioinformatics integration, geographic expansion, and strategic collaborations with healthcare and research institutions. Investments in long-read sequencing, automation, and AI-driven analytics remain central to competitive differentiation.
Conclusion
The DNA sequencing market is experiencing strong and sustained growth, driven by rapid technological advancements, expanding clinical applications, and increasing integration of genomics into routine healthcare and pharmaceutical research. With the market valued at USD 12.31 billion in 2025, projected to reach USD 13.36 billion in 2026, and expected to expand to USD 27.25 billion by 2034, the industry reflects robust long-term potential. Rising adoption of whole genome and targeted sequencing in oncology, rare disease diagnosis, and personalized medicine, along with growing use in drug discovery and biomarker development, is strengthening market demand. Although challenges such as shortage of skilled professionals, data interpretation complexity, and privacy concerns persist, continuous innovation in next-generation and third-generation sequencing platforms, integration of AI-driven bioinformatics, and expanding government-supported genomics initiatives are expected to further accelerate market adoption across developed and emerging regions.
Segmentation By Products & Services
By Technique
By Type
By Application
By End-user
By Region