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市場調查報告書
商品編碼
1372033
2030 年 DNA 定序市場預測:按產品、技術、用途、最終用戶和地區進行的全球分析DNA Sequencing Market Forecasts to 2030 - Global Analysis By Product (Consumables, Instruments and Services), Technology (Next-Generation, Sequencing, Third Generation DNA Sequencing and Other Technologies), Application, End User and By Geography |
根據 Stratistics MRC 的數據,2023 年全球 DNA 定序市場規模將達到 125 億美元,預計在預測期內將以 19.1% 的年複合成長率成長,到 2030 年將達到 425 億美元。
DNA 定序是一種使用廣泛的平行性來確定不同 DNA 鏈序列的過程。與微陣列和其他遺傳分析技術相比,DNA 定序的優點包括成本低、準確度高、速度快,即使輸入樣本量少也能得到可靠的結果。 DNA 定序的用途包括生物標記鑒定、腫瘤學研究、個體化醫療保健和法醫學。
據國家人類基因組研究所稱,持續的技術創新將導致 2021 年 8 月每個基因組的 NGS 成本為 562 美元,每兆鹼基為 0.006 美元。
DNA 定序產業對基因組定序的需求量很大,因為它徹底改變了各個領域。此外,由於基因診斷、個人化醫療和癌症研究中對基因組定序的需求,臨床應用也不斷增加。此外,隨著基因組學不斷揭示潛在的疾病機制和潛在的治療方法,對基因組定序的需求預計會增加。這將加速 DNA 定序儀的新產品開發和市場開拓。
DNA 定序技術的高成本是市場的主要障礙。這些成本包括設備、消耗品和資料處理,使得定序配合措施通常在經濟上造成負擔。此外,定序計畫需要研究機構、臨床實驗室和醫療機構提供大量資金,而高昂的成本限制了尖端定序技術的取得,特別是在資源有限的環境中,並可能阻礙普及。這阻礙了市場的擴張。
DNA 定序技術的發展徹底改變了基因組研究和臨床應用。此外,Illumina和Oxford Nanopore等公司的次世代定序(NGS)技術使高通量定序成為可能。此外,這些發展使得大規模基因組研究變得更加經濟實惠,並加快了資料收集速度。單分子定序和長讀長技術提高了 DNA 序列的準確性,使得分析複雜的基因組區域變得更容易。此外,它允許研究人員和臨床醫生在從農村地區到臨床設施的各種環境中進行定序活動,從而提高了基因組學的可及性和有效性。因此,這些要素是市場擴張的主要驅動力。
DNA 定序市場一直受到隱私問題的阻礙。隨著基因檢測的使用增加,人們和組織對敏感基因資料的安全性和潛在濫用提出了擔憂。此外,這阻礙了人們參與基因研究和與醫療保健專業人員共用資訊,從而減緩了基因組學研究和治療應用的發展。此外,現代定序技術會產生大量資料,造成巨大的計算和資料分析障礙,阻礙有效的解釋和利用。
DNA 定序市場受到了 COVID-19 爆發的負面影響。疫情擾亂了供應鏈,限制了實驗室的使用,並給醫療機構造成了財務限制,從而影響了測序計劃和非大流行項目的研究經費。儘管有這些挑戰,大流行加速了定序在感染疾病研究中的引入,並逐漸限制了市場擴張。
由於文庫建構各個階段(包括 DNA 片段化、富集、接頭連接、擴增和品管)的試劑和試劑盒廣泛可用,消耗品部分預計將佔據最大佔有率。它還包括用於樣品製備和分析的消耗品、流通池、引子、緩衝液和定序試劑。消耗品對於定序工作流程至關重要,因為它們可確保 DNA 序列的準確性和有效性。因此,消耗品產業為製造商提供了重要且穩定的收入來源,對於基因組學研究、臨床診斷和個人化醫療的進步至關重要。
預計次世代定序領域將在預測期內出現良好的成長。 NGS 因其能夠以實惠的價格產生高品質的序列資料而成為主流定序方法。此外,NGS 已被證明比傳統定序技術更準確,使其適合癌症檢測和基因組研究等用途。此外,稱為次世代定序儀定序儀(NGS)系統的大規模平行定序儀可以在短時間內產生大量資料。因此,次世代定序儀技術憑藉其優越的準確性和檢測能力,有望獲得更大的市場佔有率。
由於該地區經濟體的積極參與,亞太地區在預測期內獲得了最大的市場佔有率。此外,該地區許多國家啟動了大規模的基因組學計劃和研究計劃。鼓勵基因組在醫療保健中應用的重要舉措的例子包括日本的日本基因組醫學計劃和中國的精準醫學計劃。此外,政府資助以及與大企業的合作也支持該領域的創新。亞太地區龐大的人口為基因檢測和個人化醫療創造了龐大的市場。因此,該地區正在成為擴大基因組研究和 DNA 定序領域的焦點。
預計歐洲在預測期內的年複合成長率最高。該地區受益於充滿活力的科學界、受人尊敬的研究機構以及促進基因組學研究創造力和金融投資的友好法規環境。此外,歐洲國家對醫療保健的大量投資增加了對個人化醫療、遺傳診斷和藥物基因組學中基因組應用的需求。此外,國際合作鼓勵大規模基因組學配合措施,加劇該地區的競爭。因此,歐洲的全民健保體係有利於將基因組資料涵蓋臨床實踐並刺激市場擴張。
According to Stratistics MRC, the Global DNA Sequencing Market is accounted for $12.5 billion in 2023 and is expected to reach $42.5 billion by 2030 growing at a CAGR of 19.1% during the forecast period. DNA sequencing is a procedure that uses extensive parallelization to sequence different DNA strands. The advantages of DNA sequencing over microarray and other genetic analysis techniques include cheaper cost, higher accuracy and speed, and reliable results even with small sample input, applications for DNA sequencing include the identification of biomarkers, oncology research, individualized healthcare, forensics, and others.
According to National Human Genome Research Institute, due to continuous innovations, the cost of NGS per genome is USD 562, and the cost of NGS per megabase is USD 0.006 in August 2021.
Genome sequencing is in greater demand in the DNA sequencing industry due to its transformational effects across a number of fields. Additionally, a rise in clinical applications is being caused by the necessity of genome sequencing in genetic diagnostics, customized medicine, and cancer research. Furthermore, the need for genome sequencing is anticipated to increase as genomics continues to shed light on the mechanisms underlying disease and potential treatments. Thus, this will encourage new product development and market expansion for DNA sequencing.
The high cost of DNA sequencing technologies is a key market obstacle. Equipment, consumables, and data processing are included in these costs, which frequently make sequencing efforts financially burdensome. Additionally, sequencing programs require huge amounts of cash from research institutions, clinical laboratories, and healthcare facilities, particularly in environments with limited resources, high expenses can restrict access to cutting-edge sequencing techniques and deter widespread adoption. Therefore, hampers the market expansion.
Genomic research and clinical applications have undergone a revolution due to technological developments in DNA sequencing. Additionally, high-throughput sequencing is made possible by next-generation sequencing (NGS) technologies from companies like Illumina and Oxford Nanopore. Moreover, because of the developments, large-scale genomic studies it has become more affordable, and data gathering has been speed up. The accuracy of DNA sequencing has increased because of single-molecule sequencing and long-read technologies, which also make it easier to analyze complex genomic areas. Furthermore, this has increased the accessibility and effect of genomics by enabling researchers and clinicians to conduct sequencing activities in a variety of contexts, from rural locations to clinical facilities. Therefore, these factors significantly have driven the market expansion.
The market for DNA sequencing has been hampered by privacy issues, as the use of genetic testing increases, people and organizations express concern about the security and potential abuse of highly sensitive genetic data. Additionally, this has made people hesitant to take part in genetic research and share information with healthcare professionals, which has slowed the development of genomics research and therapeutic applications. Furthermore, modern sequencing technologies create enormous amounts of data, which poses substantial computing and data analytic obstacles and hampers effective interpretation and utilization.
The market for DNA sequencing was negatively impacted by the COVID-19 epidemic. The pandemic impacted sequencing initiatives and research funding for non-pandemic projects by disrupting the supply chain, limiting laboratory access, and creating financial restrictions in healthcare institutions. Despite these challenges, the pandemic accelerated the adoption of sequencing for the research of infectious diseases, which gradually restrained market expansion.
The consumables segment is estimated to hold the largest share, due to the widespread availability of reagents and kits for all library construction phases, including DNA fragmentation, enrichment, adapter ligation, amplification, and quality control. Additionally, this includes consumables used for sample preparation and analysis, flow cells, primers, buffers, and sequencing reagents. Consumables are essential to the sequencing workflow because they guarantee the precision and effectiveness of DNA sequencing. Therefore, the consumables industry provides manufacturers with a crucial and consistent source of income and is essential to the advancement of genomics research, clinical diagnostics, and customized medicine.
The next-generation sequencing segment is anticipated to have lucrative growth during the forecast period, due to its capacity to produce high-quality sequence data at affordable prices, NGS has become the predominant sequencing methodology. Furthermore, NGS has been shown to be more accurate than conventional sequencing techniques, making it appropriate for uses like cancer detection and genomics research. Moreover, massively parallel sequencers called next-generation sequencing (NGS) systems can produce a lot of data in a short amount of time. Therefore, due to its excellent accuracy and detection capacities, next-generation sequencing technology is anticipated to gain a greater market share.
Asia Pacific commanded the largest market share during the extrapolated period due to the active participation of the region's economies. Additionally, many nations in the region have started large-scale genomics initiatives and research plans. Examples of significant initiatives encouraging genomics applications in healthcare include Japan's "Japanese Genomic Medicine Program" and China's "Precision Medicine Initiative". Furthermore, governmental funding and partnerships with business titans are also encouraging innovation in the sector. The enormous population of the Asia-Pacific area creates a sizable market for genetic testing and tailored medicine. Thus, as a result, the area is gradually becoming a focus for genomics research and the expansion of the DNA sequencing sector.
Europe is expected to witness highest CAGR over the projection period. The area benefits from a vibrant scientific community, esteemed research institutions, and a friendly regulatory environment that promotes creativity and financial investment in genomics research. Additionally, the demand for genomic applications in personalized medicine, genetic diagnostics, and pharmacogenomics has increased as a result of significant investments made in healthcare in European nations. Furthermore, large-scale genomics initiatives are encouraged by international cooperation, which raises the region's competitiveness. Therefore, the universal healthcare systems in Europe make it easier to incorporate genomic data into clinical practice, which stimulates market expansion.
Some of the key players in the DNA Sequencing Market include: Agilent Technologies Inc., Pacific Biosciences of California Inc., Hamilton Thorne Biosciences, Bio-Rad Laboratories Inc., Danaher Corporation, Hoffmann-La Roche Ltd, Illumina Inc., Merck KGaA, Qiagen, PerkinElmer Inc., Macrogen Inc., Myriad Genetics Inc. and Eurofins Scientific.
In March 2023, llumina Inc. a global leader in DNA sequencing and array-based technologies, announced that its first product based on its novel Illumina Complete Long Read technology is now available to order.
In September 2022, Illumina, Inc. announced the launch of the NovaSeq™ X Series (NovaSeq X and NovaSeq X Plus), new production-scale sequencers that will push the limits of what is possible with genomic medicine, enabling faster, more powerful, and more sustainable sequencing.
In January 2019, NRGene and Macrogen Corp announced the launch of a joint sequencing-based genotyping service, ArrayMAGIC, at the Plant and Animal Genome (PAG) conference in San Diego.