Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us

Download Mobile App




Uptake of Next-Generation Sequencing in Europe Driven Largely by Personalized Medicine Developments

By LabMedica International staff writers
Posted on 02 Jun 2014
A new Frost & Sullivan (San Antonio, TX, USA) analysis has found the Western European next-generation sequencing (NGS) market poised for steady growth, owing to the emergence of many new applications.

The new report, "Western European Next-Generation Sequencing Markets," indicates that growth will continue with the emergence of applications such as noninvasive prenatal testing and comprehensive oncology panels. More...
NGS companies are further tapping into this space by forming partnerships with molecular diagnostic companies to quicken NGS adoption in clinics, particularly for oncology-based testing. Also, the future of DNA sequencing is predicted to shift from a laboratory-based setup to point-of-care testing in the next 5 years.

The report found that the market earned revenues of USD 381.9 million in 2013 and estimates this to reach USD 697.3 million in 2018. The total market, as defined by this study, includes next-generation sequencers and reagents for both research and diagnostic use. Major medical growth areas will include preimplantation genetic diagnosis, oncology testing, infectious disease, human leukocyte antigen typing, and companion diagnostics. Also, as applications expand to include food and safety testing (as well as crop improvement), ready-to-use sequencing-based tests that generate data from raw samples will emerge as important tools.

A key restraint curbing market potential is the lack of reimbursement norms, which leads to geographical disparity in terms of NGS test availability. The consequent need for the cross-border shipping of samples, prominent in Belgium, France, Italy, Spain, the UK, and Germany, makes gauging the reimbursement scenario extremely tough for market participants. Hence, NGS vendors must establish early, robust partnerships with regulatory bodies and devise effective business models to gain rapid regulatory clearance. Manufacturers must also look to adhere to the CE marking rather than laboratory developed test (LDT) policies to enable the easy generation of reimbursement codes.

"Companies within the space of personalized healthcare are designing instruments to target specific needs across the clinical diagnostic spectrum, therefore adding NGS capabilities to their portfolio," said Divyaa Ravishankar, Healthcare Senior Industry Analyst at Frost & Sullivan. "As long as the genomic era interfaces with personalized medicine, NGS uptake will continue."

"Given the recent technology advancements in Europe, the future of DNA sequencing will move away from a laboratory-based setup to point-of-care testing," predicted Ms. Ravishankar. "Frost & Sullivan expects NGS to become an area of interest to all market leaders within the point-of-care testing domain, as they strive to bring sequencing from 'bench to bedside'."

Related Links:

Frost & Sullivan
Life Sciences Growth Partnership Service program



Gold Member
Hematology Analyzer
Medonic M32B
POC Helicobacter Pylori Test Kit
Hepy Urease Test
New
Gold Member
Genetic Type 1 Diabetes Risk Test
T1D GRS Array
Clinical Chemistry System
P780
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Immunology

view channel
Image: Whole-genome sequencing enables broader detection of DNA repair defects to guide PARP inhibitor cancer therapy (Photo courtesy of Illumina)

Whole-Genome Sequencing Approach Identifies Cancer Patients Benefitting From PARP-Inhibitor Treatment

Targeted cancer therapies such as PARP inhibitors can be highly effective, but only for patients whose tumors carry specific DNA repair defects. Identifying these patients accurately remains challenging,... Read more

Pathology

view channel
Image: AI models combined with DOCI can classify thyroid cancer subtypes (Photo courtesy of T. Vasse et al., doi 10.1117/1.BIOS.3.1.015001)

AI-Powered Label-Free Optical Imaging Accurately Identifies Thyroid Cancer During Surgery

Thyroid cancer is the most common endocrine cancer, and its rising detection rates have increased the number of patients undergoing surgery. During tumor removal, surgeons often face uncertainty in distinguishing... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.