29 November 2019
Visiongain has launched a new pharma report ‘’Next-Generation Sequencing (NGS) Services Market Report’’ by Service Type (Human Genome Sequencing Services, Single Cell Sequencing Services, Microbial Genome - based Sequencing Services, Animal & Plant Sequencing, Gene Regulation Services (Small RNA sequencing service, ChIP sequencing, Other gene regulation - based service), Other Sequencing Services), Workflow (Data Analysis Service, Pre Sequencing Service, Sequencing Service), End Users (Hospitals & Clinics, Pharma & Biotech, Universities & Other Research Facilities, Other End Users), and Geography.
The global next-generation sequencing (NGS) Services market is anticipated to grow at a lucrative CAGR of 13.8% and anticipated to reach USD 6.49 billion by 2030.
In terms of reproducibility and cost savings, the advancement of NGS technology has revolutionized gene sequencing. As a result, many developments in NGS technology have been made to facilitate its use in medical laboratories and hospitals. Most of the current innovations in the NGS industry spin around the simplification & sophistication in the usage of seq-technology. Such factors have motivated several end-users to take up NGS services.
Service providers of traditional disease testing have increased their scope with an increasing trend in sequential genetic testing. For instance, ARUP Laboratories collaborated with the CHOP (Children's Hospital of Philadelphia) in October 2014. In November 2017, service provision for HLA genotyping based on NGS, including HLA Class I & II, began.
With the rising trend of high-performance sequencing in the pharmaceutical and biotech industries, further innovations are needed to improve the speed and convenience of seq-platforms with high-performance and simplify workflows. As a result, companies are focusing on developing approaches to improve sample amplification and purification.
The new Small RNA Library Prep Kit for Illumina was launched by Norgen in July 2017. This kit is being designed to produce small RNA libraries and is configured for low-input RNA (0.5-1ng) samples such as urine, saliva, plasma, blood, and exosomes.
Data generated by genome sequencing is considered as an important diagnostic method which enables clinicians to identify specific characteristics in the patient, thus helping clinicians with tailored treatments, thus increasing clinical results. In the coming years, this aspect is expected to fuel demand for NGS-based diagnostics.
However, some of the major issues faced by customers while conducting single-cell seq are introducing large-scale data analysis and analytical problems. Nonetheless, manufacturers are actively investing in research & development to tackle these obstacles and increase the scope of next-generation sequencing services.
On the other hand, during the forecast period, gene regulatory services were expected to show a lucrative CAGR. This includes small sequencing of RNA, ChIP-sequencing, sequencing of lncRNA, isoform sequencing and sequencing of bisulfite. In many applications, numerous advantages provided by RNA sequencing have allowed microarrays to be replaced. The application of RNA-seq is expected to continue to expand in the coming years, driving rapid growth in the field.
Researchers engaged in performing sequencing protocols for their projects face great challenges in analyzing NGS results. This is because of the effective collection and interpretation of data requires a structured and knowledgeable methodology. As the number of sequenced reads per run increases, there is expected a resulting increase in demand for a reliable data management solution.
In the year 2018, North America dominated the global next-generation sequencing market owing to factors such as well-established computer networks, successful regulatory guidelines for genetic testing acceptance and use, and the presence of major players in the region. Also, increasing numbers of genomic tests approved by the FDA in the U.S. are expected to drive the regional market throughout the forecast period.
The Asia Pacific next-generation sequencing market is anticipated to grow at a lucrative CAGR over the forecast period owing to growing government investments in the development of advanced diagnostic approaches. Also, domestic players in Asian countries are involved in establishing mutually beneficial alliances for the establishment of NGS service providers, as well as with global companies. For example, Novogene (China) partnered with AITbiotech based in Singapore in 2017 to set up NovogeneAIT Genomics Singapore Pte Ltd. to provide next-generation sequencing services across Southeast Asian countries.
Currently, key players are forming various strategies such as acquisitions, mergers, partnerships, collaborations and launching new products to strengthen their position in the global next-generation sequencing (NGS) market. Companies are also expanding their R&D, distribution, and management facilities to expand their business and to hold a competitive edge in the NGS Services market.
The comprehensive market report features companies such as Abm Inc., ARUP Laboratories, BGI, Gene by Gene, GENEWIZ Germany GmbH, Illumina, Inc., Lucigen, NanoString Technologies, Inc., Novogene Corporation, Pacific Biosciences of California, Inc., Quest Diagnostics, Veritas Genetics, SeqLL Inc., CD Genomics, Otogenetics Corporation, DNA Link, Inc., MedGenome Inc., SciGenom Labs Pvt. Ltd, PerkinElmer, Inc., Qiagen N.V. among other prominent players. Also the research study offers market estimation and forecast for the period ranging 2020-2030 for global markets such as North America, Latin America, Europe, Asia Pacific and MEA along with regional sub-markets as U.S., Canada, Brazil, Mexico, Germany, UK, France, Italy, Spain, Russia, India, Japan, China, Australia, ASEAN, GCC and South Africa.
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