![]() |
市場調査レポート
商品コード
1630617
ロングリードシーケンスの市場規模、シェア、成長分析:提供製品別、技術別、ワークフロー別、用途別、エンドユーザー別、地域別 - 産業予測 2025~2032年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 |
||||||
|
ロングリードシーケンスの市場規模、シェア、成長分析:提供製品別、技術別、ワークフロー別、用途別、エンドユーザー別、地域別 - 産業予測 2025~2032年 |
出版日: 2025年01月09日
発行: SkyQuest
ページ情報: 英文 157 Pages
納期: 3~5営業日
|
ロングリードシーケンスの世界市場規模は2023年に5億9,581万米ドルと評価され、2024年の7億7,992万米ドルから2032年には67億2,302万米ドルに拡大し、予測期間(2025年~2032年)のCAGRは30.9%で成長する見通しです。
遺伝子シーケンシング市場は、遺伝性疾患の発生率の増加、個別化医療の台頭、第3世代シーケンシングのような技術の進歩によって牽引されています。COVID-19のパンデミックは、診断や医薬品開発における革新的なシーケンス手法の需要をさらに加速させています。単一分子リアルタイム(SMRT)やナノポア(Nanopore)などのロングリードシーケンス技術は、複雑なゲノム領域を正確に解析し、従来の方法では見逃されがちな大規模な構造異常を検出できるため、人気を集めています。これらの利点により、特に遺伝性疾患について、より効率的な診断が可能になります。さらに、医薬品開発やコンパニオン診断のための先進ゲノム技術開発を目的とした提携に見られるように、大手企業による投資の増加が市場の成長を促進すると予想されます。
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.