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市場調査レポート
商品コード
1289651
ロングリードシーケンス市場- 世界の産業規模、シェア、動向、機会、予測、2017年~2027年:コンポーネント別、技術別、ワークフロー別、用途別、エンドユーザー別、企業別、地域別セグメントLong Read Sequencing Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, 2017-2027 Segmented By Component, By Technology, By Workflow, By Application, By End User, By Region, By company and By Region |
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カスタマイズ可能
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ロングリードシーケンス市場- 世界の産業規模、シェア、動向、機会、予測、2017年~2027年:コンポーネント別、技術別、ワークフロー別、用途別、エンドユーザー別、企業別、地域別セグメント |
出版日: 2023年06月01日
発行: TechSci Research
ページ情報: 英文 113 Pages
納期: 2~3営業日
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ロングリードシーケンスの世界市場は、予測期間2023-2027年に目覚ましい成長を遂げると予測されています。
主な要因としては、遺伝性疾患の新興国市場の拡大、研究開発活動に対する政府支援の拡大、技術の広範な開拓などが市場の成長を後押ししています。ロングリードシーケンスは、第3世代シーケンシングとも呼ばれ、研究が進められているDNAシーケンシング技術です。一度に10,000~100,000塩基対の長いDNA配列の塩基配列を決定することができます。この技術により、他のDNA塩基配列決定法では通常必要とされるDNAの切断や増幅が不要となります。市場の成長を支えるその他の要因としては、研究開発活動の活発化、がんを含む遺伝性疾患患者の増加、臨床試験件数の増加、個別化医療の人気の高まり、医療診断のための最新手法の受け入れ拡大、医療機関における学術目的のシーケンス解析手法の利用拡大、世界人口の増加、無機的成長戦略の採用拡大、新興サブマーケットへの大きな可能性などが挙げられます。
色覚異常、ダウン症、嚢胞性線維症などの遺伝性疾患の世界の流行が、市場の成長を後押ししています。世界保健機関(WHO)によると、10,000を超える遺伝性疾患が単発性であることが知られており、ヒトDNA内の1つの遺伝子のエラーによって引き起こされます。ロングリードシーケンス法を用いれば、患者の全ゲノミクスを調べることができます。そのため、遺伝子疾患の治療におけるロングリードシーケンスの採用が増加しています。遺伝性疾患を患う患者数の増加も市場成長の一因です。世界保健機関(WHO)によると、重度の遺伝性疾患である鎌状赤血球貧血は、新生児の約72,000人が罹患しています。
ロングリードシーケンス法を用いた研究の増加は、政府当局から多額の資金援助を受けており、これが市場成長の主な理由となっています。さらに、研究活動の増加が市場の成長を後押ししています。例えば、米国では、ゲノム研究開発プロジェクトは、米国国立衛生研究所(NIH)だけでなく、世界中の他の多くのグループからも資金提供を受けています。現在、数多くの研究活動が行われており、これはメーカーが新しく先進的なロングリードシーケンスを開発する際に有利になるとともに、ロングリードシーケンス市場に多くの機会をもたらすと予測されています。例えば、米国では、ゲノム研究開発プロジェクトは、米国国立衛生研究所(NIH)だけでなく、世界中の他の多くのグループからも資金提供を受けています。
シーケンサーの技術的進歩の高まりが市場の成長を後押ししています。これらの進歩により、シーケンスの効率性、正確性、移植性が向上しています。例えば、SMRTシーケンサで生成されるロングリードは、可能性のある反復領域を網羅し、ゲノム全体を包括的に見ることができます。同様に、2018年、カリフォルニアのPacific Biosciences(PacBio)は、ソフトウェアの新バージョン、試薬を含む新しい消耗品、新しいSMRTセル(1M v3)からなるSequel Systemの機能強化を発表しました。
TechSci Researchは、所定の市場データを使用して、企業の特定のニーズに応じたカスタマイズを提供します。レポートでは以下のカスタマイズが可能です:
The global long-read sequencing market is anticipated to observe impressive growth during the forecast period 2023-2027. The major factors include growing occurrences of genetic disorders, growing government support for R&D activities, and extensive development in technology are fueling the growth of the market. Long-read sequencing, also known as third-generation sequencing, is a DNA sequencing technique that is being researched. It can determine the nucleotide sequence of long sequences of DNA ranging between 10,000 and 100,000 base pairs at a time. This technology eliminates the need to cut up and then amplify DNA which is usually needed in other DNA sequencing methods. The other factors supporting the market's growth are, a rise in R&D activities, a growing number of patients with genetic diseases, including cancer, an increasing number of clinical trials, the rising popularity of personalized medicine, increasing acceptance of modern approaches for medical diagnostics, rising utilization of sequence analysis methodologies in medical institutes for academic purposes, rise in world population, growing adoption of inorganic growth strategies, and immense potential for emerging submarkets.
The increasing prevalence of genetic diseases, such as color blindness, Down's syndrome, cystic fibrosis, and others, across the globe is bolstering the growth of the market. According to the World Health Organization (WHO), more than 10,000 of the diseases are known to be monogenic, triggered by a single error in a single gene in the human DNA. With the help of long-read sequencing methods, the whole genomics of the patient can be examined. Thus, rising the adoption of long-read sequencing in the treatment of genetic conditions. The growing number of patients suffering from genetic diseases is also a contributing factor to the growth of the market. According to the World Health Organization (WHO), sickle cell anemia, a severe genetic condition, affects about 72,000 newborn babies.
The increasing research which uses long-read sequencing methods is being heavily funded by government authorities, which is a key reason for the growth of the market. Moreover, the rising number of research activities is augmenting the growth of the market. For instance, in the U.S., genomics research and development projects are funded through the National Institutes of Health (NIH) as well as numerous other groups from around the globe. Presently, numerous amounts of research activities are being performed, which is projected to give manufacturers an advantage as they develop new and advanced long-read sequencing, as well as to open many opportunities in the long-read sequencing market. For instance, in the U.S., genomics research and development projects are funded through the National Institutes of Health (NIH) as well as numerous other groups from around the globe.
The rise in technological advancements in sequencers is propelling the growth of the market. These advancements have made sequencing more efficient, accurate, and portable. For instance, long reads generated by SMRT sequencers span around possible repetitive regions and give a comprehensive view of the whole genome. Similarly, in 2018, Pacific Biosciences of California (PacBio) announced the enhancements to their Sequel System, which comprises a new version of its software, new consumables including reagents, and a new SMRT Cell (1M v3).
The global long-read sequencing market is segmented into components, technology, workflow, application, end user, and company. Based on components, the market is divided into instruments, consumables, and services. Based on technology, the market is divided into single-molecule real-time sequencing (SMRT), nanopore sequencing, and others. Based on workflow, the market is divided into pre-sequencing, sequencing, and data analysis. Based on application, the market is divided into oncology, infectious diseases, rare diseases, genetic disorders, metabolic disorders, and others. Based on end-user, the market is divided into hospitals & clinics, biotechnology & pharmaceutical companies, academic & research institutions, and others. In terms of country, the United States is expected to be a lucrative market in the forecast period due to rising incidences of hematologic malignancies in the country.
Agilent Technologies, Inc., BGI Group, Bionano Genomics, Inc., Circulomics Inc, Oxford Nanopore Technologies plc, Longas Technologies Pty Ltd, Novogene Co., Ltd., Illumina, Inc., F. Hoffmann-La Roche AG, Pacific Biosciences of California, Inc., Quantapore, Inc., QIAGEN NV, PerkinElmer, Inc, Thermo Fischer Scientific, Inc., and Takara Bio, Inc. are some of the leading companies operating in the market.
In this report, global long-read sequencing market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:
Company Profiles: Detailed analysis of the major companies present in Global Long Read Sequencing Market
With the given market data, TechSci Research offers customizations according to a company's specific needs. The following customization options are available for the report: