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全基因組測序市場 - 2018-2028 年全球行業規模、佔有率、趨勢、競爭、機會及預測。按測序類型、按產品類型、按應用、按最終用戶、按地區和競爭情況分類Whole Genome Sequencing Market - Global Industry Size, Share, Trends, Competition, Opportunity, and Forecast, 2018-2028. Segmented By Sequencing Type, By Product Type, By Application, By End User, By Region and Competition |
在2024-2028 年的預測期內,全基因組測序市場預計將以驚人的複合年成長率成長。這可歸因於以下因素
NGS 儀器技術的不斷進步和測序技術的更新將進一步推動測序市場在預測期內的成長。此外,與毛細管測序或基於PCR 的方法不同,下一代測序(NGS)具有復用功能,使微生物研究人員能夠對數百種生物進行測序。基於NGS 的微生物基因組測序不僅省時高效,而且簡化了工作流程,不像老式技術那樣依賴於耗時的克隆階段。此外,可能會被忽視的低頻變異和基因組重排,使用現有技術發現成本太高,而使用NGS(下一代測序)則可以發現。此外,當今時代的群體級WES(全外顯子組測序)數據生成量也在增加。全外顯子組測序(WES)是測序領域的一項成功應用,孟德爾表型、米勒氏病等疾病的基因的發現證明了這一點。全外顯子測序比全基因組測序更有用,因為大多數已知的致病突變都發生在外顯子中,市場需求量很大,因此預計未來將推動市場成長。
全基因組測序在疾病診斷方面的臨床應用需求日益成長,在鑑定基因組片段突變以分離基因變異或突變方面具有重要意義。此外,微生物全基因組重測序等技術涉及對細菌、病毒或其他微生物的整個基因組進行測序,並將測序結果與已知參照物的序列進行比較,因此有助於疾病診斷。因此,這種微生物基因組測序是微生物鑑定的重要工具。此外,全基因組測序技術還可用於識別生物體內鹼基的排列順序,從而生成精確的DNA 指紋,有助於將病例聯繫起來,快速檢測出疾病的爆發或缺陷,因此在傳染病診斷方面具有重要意義,從而促進預測期內的市場成長。
政府項目對基因組測繪的需求不斷增加,因為與疾病診斷和研究有關的研發工作日益增多,以改善癌症、突變性疾病和其他疾病的治療等。此外,不同國家和地區的政府正在對數百萬個基因組進行測序,以促進研究,發現更好的方法來識別和治療癌症、不常見疾病和其他疾病。例如,歐洲政府正在通過法國的"2025 年法國基因組醫學計劃"和英國的"10 萬基因組計劃"等項目,努力改善該地區的大規模基因組數據。這些計劃促進了NGS 下一代測序(NGS)資訊學服務在該地區的發展。例如,2022 年11 月,斯坦福醫科大學的科學家利用奈米孔基因組測序、人工智慧和雲端運算,在不到5 個小時的時間內完成了一名患者的全基因組測序。
2021 年11 月, Illumina 和基因聯盟宣布了一項價值1.2 億美元的全球計劃- iHope 基因健康計劃。該計劃旨在為全球各種受遺傳疾病影響的患者提供全基因組測序(WGS)服務。
此外,2020 年,領先企業QIAGEN 收購了NeuMoDx Molecular,鞏固了其在自動化分子檢測市場的地位。現在,該公司將基於PCR 檢測技術的中高通量NeuMoDx 自動化解決方案作為其最新產品組合的新組成部分。
根據給定的市場數據,TechSci Research 可根據公司的具體需求提供客製化服務。報告可提供以下客製化選項:
Whole Genome Sequencing Market is expected to grow with an impressive CAGR in the forecast period 2024-2028. This can be attributed to factors such as
Whole Genome Sequencing Market (WGS) is a widely used application included in genome, microbial resequencing, and genome sequencing. It is expected to increase significantly with the growing research in genomics. Additionally, a rise in the usage of this technology against COVID-19 in sequencing the data of the COVID-19 virus is expected to drive market growth.
Whole Genome Sequencing Market (WGS) technology can deliver quick results and high-quality data. It can be used to locate, monitor, and address disease outbreaks in a region. WGS is shown to be most useful in research and rarely in therapeutic treatments.
The mapping of novel organisms' genomes, the completion of the genomes of already-known organisms, or the comparison of genomes from other samples all benefit from microbial whole-genome sequencing. To create reliable reference genomes, microbial identification, and other comparative genomic investigations, it is required to sequence the full bacterial, viral, and other microbial genomes.
Increasing technological advancement in NGS instruments and update in technology utilized in Sequencing techniques are adding to further drive the sequencing market growth in the forecast period. Moreover, with its multiplexing feature, next-generation sequencing (NGS) enables microbiology researchers to sequence hundreds of organisms, unlike capillary sequencing or PCR-based methods. NGS-based microbial genome sequencing is time efficient and streamlines the workflow, and does not rely on time-consuming cloning stages like older techniques. Additionally, low-frequency variations and genomic rearrangements that might be overlooked are too expensive to find using current techniques that can be found using NGS (Next Generation Sequencing). Also, population-level WES (whole exome sequencing) data generation has increased in today's time. Whole exome sequencing (WES) is a successful application in the field of sequencing and is proved by the discovery of the genes for the conditions such as Mendelian phenotypes, Miller's disease, and other diseases. Whole exome sequencing is more useful than whole genome sequencing since the majority of known disease-causing mutations take place in exons and are in high demand in the market and thus anticipated to propel the market growth in the future.
Whole genome sequencing has an increased demand in clinical applications regarding disease diagnosis and has significant importance in the identification of a mutation in a genome segment for isolating a variant or mutation in a gene. Moreover, techniques such as Microbial whole-genome resequencing involve the sequencing of the entire genome of a bacteria, virus, or other microbe and comparing the sequence to that of a known reference and thus is helpful in disease diagnosis. This microbial genome sequencing is thus an important tool for microbial identification. Additionally, the whole genome sequencing technique is used for identifying the order of bases in the organism and is thus utilized to produce a precise DNA fingerprint and thus can aid in linking the cases allowing the eruption or defect to be detected quickly and, thus, is significant in infectious disease diagnosis to bolster the market growth in the forecast period.
The rising demand for genome mapping in government projects for the rising research and development related to disease diagnosis and research for improved treatment in cancer, mutated disorders, and other diseases, etc. Furthermore, governments of distinct countries and regions are sequencing millions of genomes to progress research and discover better ways to identify and cure cancer, uncommon disorders, and other ailments. For instance, the European government is undertaking efforts to improve the region's large-scale genomic data with projects such as France's French Plan for Genomic Medicine 2025 and, similarly, the United Kingdom's 100,000 Genomes Project. These initiatives have resulted in the growth of NGS's Next-generation sequencing (NGS) informatics services in the region. For instance, in November 2022, using Nanopore Genome Sequencing, AI, and Cloud Computing, scientists at Stanford Medicine University sequenced a patient's whole genome in under five hours.
In November 2021, Illumina and Genetic Alliance announced a USD 120 million global initiative-the iHope Genetic Health program. This initiative aims to offer Whole Genome Sequencing (WGS) access to various patients impacted by genetic disorders globally.
Also, In 2020, a leading company QIAGEN acquired NeuMoDx Molecular and secured its position in the market in automated molecular testing. The company now includes medium- and high-throughput NeuMoDx automation solutions based on PCR testing technology as a new component of its updated product portfolio.
The whole Genome Sequencing Market is segmented based on the sequencing type, product type, application, end-user, and region. Based on sequencing type, the market is segmented into large whole-genome sequencing and small-genome sequencing. Based on product type, the market is segmented into instruments, kits, and services. Based on application, the market is segmented into diagnostics, drug discovery and development, personalized medicine, and others. Based on end users, the market is further fragmented into hospitals and clinics, pharmaceutical and biotechnology companies, and others. Based on the region, the market is further segmented into North America, Europe, Asia-Pacific, South America, and MEA.
GE Healthcare, Inc., Illumina, Inc., QIAGEN N.V., Thermo Fisher Scientific, Agilent Technologies, 10 x Genomics, BGI, Oxford Nanopore, Nebula Genomics, Veritas Genetics, etc.., are some of the major players operating in the global Whole Genome Sequencing Market.
In this report, Whole Genome 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 Whole Genome 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: