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市场调查报告书
商品编码
1630617
长读定序市场规模、份额和成长分析:按产品供应、按技术、按工作流程、按应用、按最终用户、按地区 - 2025-2032 年行业预测Long Read Sequencing Market Size, Share, Growth Analysis, By Offerings, By Technology, By Workflow, By Application, By Usage, By End Users, By Region - Industry Forecast 2025-2032 |
2023年,全球长读定序市场规模为5.9581亿美元,从2024年的7.7992亿美元扩大到2032年的67.23亿美元,在预测期内(2025-2032年)预计将以30.9的复合年增长率增长。
基因定序市场受到遗传疾病发生率上升、个人化医疗兴起以及第三代定序等技术进步的推动。 COVID-19 大流行进一步加速了诊断和药物开发中对创新测序方法的需求。单分子即时(SMRT)和奈米孔等长读长定序技术越来越受欢迎,因为它们可以准确分析复杂的基因组区域并检测我收集的传统方法经常遗漏的大规模结构异常。这些优点可以实现更有效的诊断,尤其是遗传性疾病。此外,领先公司增加投资预计将推动市场成长,正如旨在开髮用于药物开发和伴同性诊断的先进基因组技术的合作所反映的那样。
Global Long Read Sequencing Market size was valued at USD 595.81 million in 2023 and is poised to grow from USD 779.92 million in 2024 to USD 6723.02 million by 2032, growing at a CAGR of 30.9% during the forecast period (2025-2032).
The market for genetic sequencing is being driven by the increasing incidence of genetic disorders, the rise of personalized medicine, and advancements in technologies like third-generation sequencing. The COVID-19 pandemic has further accelerated the demand for innovative sequencing methods in diagnostics and drug development. Long read sequencing techniques, such as Single Molecule Real Time (SMRT) and Nanopore, are gaining traction due to their ability to accurately analyze complex genomic regions and detect large structural abnormalities that traditional methods often miss. These advantages allow for more efficient diagnostics, particularly for genetic disorders. Additionally, increased investments from major companies are expected to propel market growth, as seen in partnerships aimed at developing advanced genomic technologies for drug development and companion diagnostics.
Top-down and bottom-up approaches were used to estimate and validate the size of the Global Long Read Sequencing market and to estimate the size of various other dependent submarkets. The research methodology used to estimate the market size includes the following details: The key players in the market were identified through secondary research, and their market shares in the respective regions were determined through primary and secondary research. This entire procedure includes the study of the annual and financial reports of the top market players and extensive interviews for key insights from industry leaders such as CEOs, VPs, directors, and marketing executives. All percentage shares split, and breakdowns were determined using secondary sources and verified through Primary sources. All possible parameters that affect the markets covered in this research study have been accounted for, viewed in extensive detail, verified through primary research, and analyzed to get the final quantitative and qualitative data.
Global Long Read Sequencing Market Segmental Analysis
Global Long Read Sequencing Market is segmented by Offerings, Technology, Workflow, Application, Usage, End Users and region. Based on Offerings, the market is segmented into Consumables, Instruments and Services. Based on Technology, the market is segmented into Nanopore sequencing, Single-molecule real-time sequencing and Synthetic long-read sequencing. Based on Workflow, the market is segmented into Sequencing, Sample Preparation and Data analysis. Based on Application, the market is segmented into Whole Genome Sequencing, Targeted Sequencing, Metagenomics, Epigenetics, Whole exome sequencing and Other applications. Based on Usage, the market is segmented into Research and Clinical. Based on End Users, the market is segmented into Academic & Research Institutes, Hospitals, Clinics & Diagnostic Labs, Pharmaceutical & Biotechnology Companies and Other End Users. Based on region, the market is segmented into North America, Europe, Asia Pacific, Latin America and Middle East & Africa.
Driver of the Global Long Read Sequencing Market
The Global Long Read Sequencing market is significantly propelled by the growing adoption of next-generation sequencing (NGS) technologies across diverse research domains such as genomics, transcriptomics, and epigenomics. These advanced sequencing methods enable researchers to obtain deeper insights into critical areas like genome assembly, gene expression, and DNA modification patterns. By enhancing the accuracy and completeness of genomic data, long read sequencing becomes an essential tool in NGS-based studies, further driving its implementation in various scientific investigations. This increasing demand for comprehensive genomic analysis fosters the overall growth of the long read sequencing market on a global scale.
Restraints in the Global Long Read Sequencing Market
The global Long Read Sequencing market faces several restraints, notably the high expenses associated with these advanced technologies. Compared to conventional short read sequencing, long read sequencing incurs greater costs related to equipment, reagents, and data analysis. This financial burden can restrict the implementation of long read sequencing methods, particularly in clinical diagnostics and resource-limited research environments, where budget constraints may hinder the widespread adoption of these innovative yet expensive sequencing options. Consequently, the elevated costs present a significant challenge for the growth and accessibility of long read sequencing in various sectors.
Market Trends of the Global Long Read Sequencing Market
The Global Long Read Sequencing market is witnessing robust growth as healthcare and research institutions increasingly adopt these advanced technologies for their superior ability to deliver comprehensive genomic insights. This shift is primarily fueled by the need for accurate genome assembly, structural variant analysis, and complex transcriptomic studies, which short read sequencing often struggles to address. Moreover, the expanding applications in personalized medicine, oncology, and genetic research are amplifying market demand, while technological advancements and reduced costs further enhance accessibility. As a result, long read sequencing is positioning itself as a pivotal tool in the genomics landscape, shaping the future of precision medicine and genetic research.