![]() |
市場調查報告書
商品編碼
2086946
次世代定序:市場洞察、競爭格局與市場預測(2034 年)Next Generation Sequencing - Market Insights, Competitive Landscape, and Market Forecast - 2034 |
||||||
次世代定序市場概述
次世代定序(NGS),也稱為高通量定序或大規模定序,是指一系列能夠並行讀取數百萬個DNA或RNA片段的技術,可在數小時內而非數年內產生全基因組、全EXOME或標靶定序資料。此類別包括基於合成定序和半導體定序的短讀長平台,以及長讀長單分子定序和奈米孔系統,所有定序都依賴包含樣品製備耗材、儀器、生物資訊軟體和外包定序服務的工作流程。在過去的十年中,NGS已從一種研究工具發展成為一種臨床基礎設施,廣泛應用於腫瘤學、生殖醫學、罕見疾病診斷、感染疾病監測和藥物基因體學等領域。
次世代定序市場的主要市場促進因素
推動次世代定序市場成長的因素
市場促進因素
定序成本的快速下降正在推動其廣泛應用。
人類基因定序的成本已從2001年的約9,500萬美元大幅下降至2022年的5.25億美元,領先的高通量定序中心在2023年實現了「200美元基因組」的目標。成本的顯著降低使NGS從以研究為中心的技術轉變為一種經濟高效的臨床和公共衛生工具,從而在腫瘤學、罕見疾病診斷、生殖醫學和大規模篩檢計畫中得到更廣泛的應用。
全球癌症負擔日益加重,加速了基因組分析的需求。
癌症發生率的不斷上升一直是推動新一代定序(NGS)技術應用的主要動力。根據國際癌症研究機構(IARC)統計,2022年全球新增癌症病例約2,000萬例,預計2050年將達到3,500萬例。隨著精準腫瘤學和標靶治療逐漸成為標準療法,全面的基因組分析和伴隨診斷對於治療方案的選擇變得日益重要,從而推動了對基於NGS的檢測及其相關耗材的需求。
市場限制因素
儘管發展勢頭強勁,但次世代定序(NGS) 市場仍面臨諸多限制因素。基於 NGS 的體外診斷 (IVD) 仍然非常複雜,因為需要適應不斷變化的美國食品藥物管理局(FDA)、歐洲體外診斷醫療器材法規 (IVDR) 以及各國臨床實驗室框架,這延長了新檢測方法的上市時間。設備購買成本高昂,耗材支出佔比也高,這意味著每個基因組的實際成本高於公佈的數據,限制了小規模檢查室採用該技術。此外,生產和供應鏈的限制,包括對少數試劑和流動池供應商的依賴,也使檢查室面臨供應風險。保險覆蓋範圍因地區和適應症而異,腫瘤學和產前檢測領域已實現全面覆蓋,但在更廣泛的應用領域則缺乏統一標準。最後,熟練的生物資訊學家短缺,以及數據存儲、解釋和臨床報告的負擔(有時被稱為“1000 美元基因組”背後的“100000 美元分析”),限制了處理能力,並延緩了資源受限環境中的採用。
競爭格局
次世代定序市場報告要點
本次世代定序市場報告的主要讀者。
Q1.次世代定序市場的成長率是多少?
預計從 2026 年到 2034 年的預測期內,次世代定序市場將以 13.9% 的複合年成長率成長。
Q2.次世代定序市場的市場規模有多大?
預計到 2025 年,次世代定序市場價值將達到 132.4 億美元,到 2034 年將達到 426.8 億美元。
Q3. 哪個地區在次世代定序市場中處於主導?
北美地區擁有密集的定序設備製造商和臨床實驗室,FDA對基於NGS的診斷產品核准流程完善,保險報銷政策優厚(包括CMS對全面基因組分析的報銷),以及聯邦政府對基因組研究的持續資助,預計將主導次世代定序市場,到2025年將佔全球銷售額的42%。亞太地區預計將成為預測期內成長最快的地區。
第四季:次世代定序市場的主要促進因素是什麼?
主要的驅動力是定序成本的快速下降。根據美國國家人類基因組研究所(NHGRI)的數據顯示,人類基因組定序的成本已從2001年的9,500萬美元降至2022年的525美元,預計到2023年將進一步降至200美元左右。國際癌症研究機構(IARC)預測,全球癌症新病例數將從2022年的2,000萬例增加到2050年的3,500萬例。此外,長讀長定定序和人工智慧驅動的生物資訊技術的成熟,以及臨床保險覆蓋範圍的擴大,也為定序成本的下降提供了推動作用。
Q5.次世代定序市場的主要參與者有哪些?
主要公司包括 Illumina、Thermo Fisher Scientific、F. Hoffmann-La Roche、QIAGEN NV、Pacific Biosciences of California, Inc.、Oxford Nanopore Technologies plc、BGI Genomics Co., Ltd.、Agilent Technologies, Inc.、Bio-Rad Laboratories, Inc. 和 Revvity, Inc.。其他活躍的製造商和服務供應商也包括在內,如“競爭格局”部分所述。
Next Generation Sequencing Market Summary
Next Generation Sequencing (NGS), also known as high-throughput or massively parallel sequencing, refers to a family of technologies that read millions of DNA or RNA fragments in parallel, producing whole-genome, whole-exome, or targeted sequence data in hours rather than years. The category spans short-read platforms based on sequencing by synthesis and semiconductor sequencing, alongside long-read single-molecule and nanopore systems, all supported by a workflow of library preparation consumables, instruments, bioinformatics software, and outsourced sequencing services. Over the past decade, NGS has moved from a research instrument into a clinical infrastructure used across oncology, reproductive health, rare disease diagnosis, infectious disease surveillance, and pharmacogenomics.
Next Generation Sequencing Market Key Growth Drivers
Key Companies in Next Generation Sequencing Market
The competitive landscape is led by the following active manufacturers and service providers:
Factors Contributing to the Growth of the Next-Generation Sequencing Market
Market Drivers
Rapid Decline in Sequencing Costs Driving Widespread Adoption
The cost of sequencing a human genome has fallen dramatically from approximately USD 95 million in 2001 to USD 525 million in 2022, with leading high-throughput centers achieving the USD 200 genome in 2023. This significant reduction has transformed NGS from a research-focused technology into a cost-effective clinical and population health tool, enabling broader adoption across oncology, rare disease diagnostics, reproductive health, and large-scale screening programs.
Increasing Global Cancer Burden Accelerating Demand for Genomic Profiling
The growing incidence of cancer continues to be a major catalyst for NGS adoption. According to the International Agency for Research on Cancer (IARC), approximately 20 million new cancer cases were diagnosed in 2022, with cases projected to reach 35 million by 2050. As precision oncology and targeted therapies become standard of care, comprehensive genomic profiling and companion diagnostics are increasingly required for treatment selection, driving demand for NGS-based testing and related consumables.
Market Restraints
Despite strong momentum, the Next Generation Sequencing market faces material constraints. Regulatory complexity remains significant, as NGS-based in vitro diagnostics must navigate evolving FDA, European IVDR, and national clinical-laboratory frameworks, lengthening time to market for new assays. High capital costs for instruments and the dominance of consumables expenditure keep the true per-genome cost above headline figures, limiting adoption among smaller laboratories. Manufacturing and supply-chain limitations, including reliance on a concentrated set of reagent and flow-cell suppliers, expose laboratories to availability risk. Reimbursement remains uneven across geographies and indications, with coverage well established for oncology and prenatal testing but inconsistent for broader applications. Finally, a shortage of skilled bioinformaticians and the burden of data storage, interpretation, and clinical reporting, sometimes described as the USD 100,000 analysis behind the USD 1,000 genome, constrain throughput and slow adoption in resource-limited settings.
Next Generation Sequencing Market Segment Analysis
The Next Generation Sequencing Market by Offering (Consumables, Instruments and Platforms, Services), Technology (Sequencing by Synthesis, Ion Semiconductor Sequencing, Single-Molecule Real-Time Sequencing, Nanopore Sequencing, Others), Application (Oncology, Reproductive Health, Clinical Investigation and Diagnostics, Drug Discovery and Personalized Medicine, Agrigenomics and Forensics, Consumer Genomics, Others), End-Users (Academic and Research Institutes, Hospitals and Clinics, Pharmaceutical and Biotechnology Companies, Clinical and Diagnostic Laboratories, Others), and Geography (North America, Europe, Asia-Pacific, Rest of World).
By Offering
Dominant Subsegment: Consumables. The consumables category is expected to dominate the market.
The consumables segment accounted for 51% of the Next Generation Sequencing market in 2025. Consumables, comprising library preparation kits, reagents, flow cells, barcodes, and target enrichment panels, are consumed on every sequencing run, producing recurring revenue that scales directly with testing volume. The structural decline in sequencing cost has expanded run volumes across oncology, reproductive health, and infectious disease testing, deepening consumables demand. Manufacturers reinforce this dynamic through bundled contracts that pair instruments with proprietary reagents, locking laboratories into recurring purchases. Recent launches illustrate continued innovation in this tier: QIAGEN introduced its QIAseq xHYB Long Read Panels in July 2025 to extend target enrichment to long-read platforms, and Illumina launched Illumina Protein Prep in September 2025 to bring proteomics into the sequencing consumables portfolio. The combination of recurring economics, expanding clinical volumes, and a steady cadence of new kit chemistries supports the segment's continued leadership across the forecast period, while the instruments and platforms tier underpins the installed base, and the services tier captures outsourced demand from laboratories that prefer not to run sequencing in-house.
By Technology
Dominant Subsegment: Sequencing by Synthesis. The sequencing by synthesis category is expected to dominate the market.
The sequencing by synthesis segment accounted for 62% of the Next Generation Sequencing market in 2025. Sequencing by synthesis is the most widely deployed NGS chemistry, valued for its high accuracy, scalability, and the lowest cost per gigabase among current platforms, which has made it the default choice for high-throughput clinical and research laboratories. Its dominance is reinforced by the breadth of validated assays, established bioinformatics pipelines, and a large global installed base of short-read instruments. Continued platform innovation sustains the segment, including ongoing throughput and cost improvements across high-capacity systems and the pursuit of the sub-USD 200 genome. Adjacent technologies are advancing rapidly: long-read single-molecule real-time and nanopore platforms are gaining share in structural variant detection and de novo assembly, and Roche introduced its sequencing-by-expansion chemistry in February 2025 as a new high-throughput approach. While these alternatives expand the technology landscape and grow quickly from smaller bases, sequencing by synthesis retains leadership through its accuracy, cost efficiency, and entrenched clinical validation across the forecast period.
By End-User
Dominant Subsegment: Academic and Research Institutes. The academic and research institutes category is expected to dominate the market.
The academic and research institutes segment accounted for 36% of the Next Generation Sequencing market in 2025. Academic and research institutes remain the largest end user because they conduct the foundational genomics, oncology, and population-scale studies that consume large volumes of sequencing capacity and consumables. National genomics programs and university medical centers operate high-throughput core facilities and sustain demand through grant-funded research, supported by ongoing public investment from agencies such as the National Institutes of Health and the National Human Genome Research Institute. These institutions are early adopters of new platforms and chemistries, driving instrument placements and consumables uptake. At the same time, the migration of NGS into routine care is enlarging the hospitals and clinics and clinical and diagnostic laboratories segments, which are growing quickly as comprehensive genomic profiling, prenatal screening, and infectious disease testing move into reimbursed clinical pathways. Pharmaceutical and biotechnology companies also contribute substantial demand through biomarker discovery and companion diagnostic development. While the clinical end users are the fastest-expanding cohort over the forecast period, academic and research institutes retain leadership in 2025 on the strength of research volume and public funding.
Next Generation Sequencing Market Region Analysis
Dominant Region: North America
North America accounted for 42% of the global Next Generation Sequencing market revenue in 2025, representing the highest regional market share globally. The region's dominance reflects the concentration of sequencing manufacturers, academic medical centers, and clinical laboratories in the United States, together with the most developed reimbursement environment for genomic testing. Market-size influence is amplified by high per-capita testing volumes in oncology and reproductive health and by early adoption of long-read sequencing. Healthcare infrastructure is mature, with comprehensive cancer centers and accredited molecular laboratories supporting routine genomic profiling. The regulatory environment is supportive: the FDA provides established pathways for NGS-based in vitro diagnostics, and the Centers for Medicare and Medicaid Services granted reimbursement of USD 2,989.55 per test for TruSight Oncology Comprehensive, effective January 2026. Disease burden is substantial, with about 2 million new cancer cases diagnosed annually in the United States, and the investment landscape is strong, sustained by National Institutes of Health and National Human Genome Research Institute funding alongside private capital concentrated in California and the Northeast.
Fastest Growing Region: Asia-Pacific
Asia-Pacific is the fastest-growing region in the Next Generation Sequencing market. The region's elevated CAGR is driven by rising healthcare investment, expanding genomic research capacity, and growing clinical adoption across China, Japan, India, South Korea, and Australia. Government initiatives, including national genomics and precision-medicine programs, are funding sequencing infrastructure and population-scale projects. Manufacturing expansion is notable, with domestic platform developers scaling production and lowering local costs. Emerging opportunities span agricultural genomics, infectious disease surveillance, and direct-to-consumer testing, supported by a large patient population and increasing collaborations between local and international companies, such as the April 2025 partnership between Gene Solutions and Element Biosciences to deliver cost-effective prenatal and oncology assays across Southeast Asia.
Regional Commentary
North America
North America accounted for 42% of the global Next Generation Sequencing market revenue in 2025. The United States dominates the region on the strength of its manufacturing base, clinical laboratory network, and reimbursement leadership, while Canada contributes through provincial genomics programs and Mexico advances population genomics initiatives such as large-scale national sequencing projects.
Europe
Europe represents the second-largest regional market, led by Germany, the United Kingdom, and France. Growth is supported by national genomics initiatives, public research funding, and the transition to the European In Vitro Diagnostic Regulation, which is raising the bar for clinical NGS assays. Oxford Nanopore's GridION Dx received CE and UKCA markings in early 2026, marking the first IVD-registered nanopore device for the region.
Asia-Pacific
Asia-Pacific is the fastest-growing region, propelled by healthcare investment, expanding research activity, and government precision-medicine programs across China, Japan, India, South Korea, and Australia. Domestic manufacturers are scaling capacity and broadening access to cost-effective sequencing, while agricultural genomics and infectious disease applications add demand beyond clinical diagnostics.
Rest of World
The Rest of World region, spanning the Middle East, Africa, and South America, is an emerging growth frontier. Rising healthcare investment, improving laboratory infrastructure, and international collaborations are expanding access. Illumina renewed its partnership with the Africa Centres for Disease Control and Prevention in March 2025 to equip national laboratories with sequencing tools, strengthening genomic surveillance capacity across the continent.
Next Generation Sequencing Market Competitive Landscape
The Next Generation Sequencing market is classified as Consolidated. A small group of global platform providers controls the majority of instrument and consumables revenue, with Illumina holding the leading position in short-read sequencing platforms, followed by Thermo Fisher Scientific in semiconductor sequencing and a long-read duopoly formed by Oxford Nanopore Technologies and Pacific Biosciences. A broader field of reagents, panels, bioinformatics, and service providers competes in the surrounding value chain.
The competitive landscape can be evaluated across the following dimensions:
Next Generation Sequencing Market Recent Developmental Activities
In January 2026, Illumina, Inc. (with the Centers for Medicare and Medicaid Services), CMS granted national reimbursement for the FDA-approved TruSight Oncology Comprehensive genomic profiling test at USD 2,989.55 per test, effective January 1, 2026. Strategic significance: Establishes durable payer support for large-panel comprehensive genomic profiling, pulling NGS oncology testing into routine reimbursed clinical practice.
In January 2026, Oxford Nanopore Technologies plc Announced that GridION Dx received CE and UKCA markings, the vendor's first in vitro diagnostic device registered in the United Kingdom and Europe, with an initial application in infectious disease characterization through a collaboration with bioMerieux to run the AmPore-TB assay for multidrug-resistant tuberculosis. Strategic significance: Positions nanopore sequencing for regulated clinical diagnostics and validates long-read platforms for infectious disease testing.
In January 2026, Pacific Biosciences of California, Inc., announced plans to collaborate with the nonprofit organizations n-Lorem Foundation and EspeRare to support development of individualized antisense oligonucleotide therapies for ultra-rare genetic disorders. Strategic significance: Extends long-read sequencing into individualized rare-disease therapeutic development, opening a differentiated clinical-research channel.
In January 2026, Daisy Genomics, Inc. (formerly Armonica Technologies) secured USD 2.5 million in seed funding led by Cottonwood Technology Fund and Tramway Venture Partners to advance a spectroscopy-based DNA and RNA sequencing platform toward commercialization. Strategic significance: Signals continued investor appetite for alternative sequencing chemistries that could broaden platform competition.
Next Generation Sequencing Market Segmentation
Next Generation Sequencing Market by Offering
Next Generation Sequencing Market by Technology
Next Generation Sequencing Market by Application
Next Generation Sequencing Market by End-Users
Next Generation Sequencing Market by Geography
Key Takeaways from the Next Generation Sequencing Market Report Study
Target audience who can benefit from this next generation sequencing market report study
Q1. What is the growth rate of the Next Generation Sequencing market?
The Next Generation Sequencing market is projected to expand at a CAGR of 13.9% during the forecast period of 2026-2034.
Q2. What is the market size of the Next Generation Sequencing market?
The Next Generation Sequencing market is estimated at USD 13.24 billion in 2025 and is projected to reach USD 42.68 billion by 2034.
Q3. Which region dominates the Next Generation Sequencing market?
North America dominated the Next Generation Sequencing market with a 42% share of global revenue in 2025, supported by a dense base of sequencing manufacturers and clinical laboratories, FDA pathways for NGS-based diagnostics, strong reimbursement, including CMS coverage of comprehensive genomic profiling, and sustained federal genomics funding. Asia-Pacific is the fastest-growing region over the forecast period.
Q4. What are the key drivers of the Next Generation Sequencing market?
The principal drivers are the collapsing cost of sequencing, with the cost per human genome falling from USD 95 million in 2001 to USD 525 by 2022 and to the USD 200 level in 2023 per the National Human Genome Research Institute; the rising global cancer burden, projected by the International Agency for Research on Cancer to increase from 20 million new cases in 2022 to 35 million by 2050; and the maturation of long-read sequencing and AI-assisted bioinformatics, reinforced by expanding clinical reimbursement.
Q5. Who are the major players in the Next Generation Sequencing market?
The major players include Illumina, Inc., Thermo Fisher Scientific Inc., F. Hoffmann-La Roche Ltd, QIAGEN N.V., Pacific Biosciences of California, Inc., Oxford Nanopore Technologies plc, BGI Genomics Co., Ltd., Agilent Technologies, Inc., Bio-Rad Laboratories, Inc., and Revvity, Inc., among other active manufacturers and service providers profiled in the Competitive Landscape section. Illumina leads short-read platforms, while Oxford Nanopore and Pacific Biosciences anchor the long-read segment.
For illustrative purposes, only the top 10 companies are listed in the Table of Contents. The report may include analysis and references to additional companies where relevant to the market assessment.