Global Genetic Testing Services Market Growth, Size, Share, Industry Report and Forecast 2019-2025
The global Genetic Testing Services market is projected to have a considerable CAGR during the forecast period. The growing prevalence of chronic diseases such as cancer, infectious diseases across the globe further contributes to the growth of the genetic testing services market. As per the International Agency for Research on Cancer (IARC), in 2018 there were 17 million new cancer cases and 9.5 million cancer mortality across the globe. Moreover, the global cancer burden is expected to grow to 27.5 million new cancer cases and 16.3 million cancer mortality in 2020.
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Increasing genomic and
proteomic researches Proteomics refers to the analysis of overall proteins
present content of a cell, tissue or an organism. It comprises of identi?cation
and quanti?cation technologies and also uses technologies such as genomics and
transcriptomics. Genomic studies and advanced technologies enable defining
driver mutation and alteration of DNA & RNA in many cancers. The genomic
information from tumors and normal tissue are compared which helps the required
genomic changes. The genomic methods are used to detect molecular
characteristics for clinical phenotypes which enables the detection of genetic
changes. Increasing investment and research in genomics and proteomics are also
significantly driving market growth.
The emerging economies such as
the Asia-Pacific region is one of the potential markets for genomic biomarkers.
The factors that will be favorable for the growth of the market in this region
include increasing government expenditures on healthcare in the region, and the
presence of a huge population suffering from various chronic diseases such as
cancer, hypertrophic cardiomyopathies, arrhythmias, and others. The average
annual increase in government healthcare spending in the US is 4.5% and less
than 1.5% in the European Union. However, the countries of Asia-Pacific
reported an increase in healthcare expenditure of more than 6%, which is higher
than the developed nations.
Moreover, the 1000 Genomes Project is an effort that comprises genome sequencing of at least a thousand people from across the globe to develop the most comprehensive and medically relevant picture of human genetic variation. This initiative intends to make accessible genomic data easily from international research institutions. The major support for the project is offered by the National Human Genome Research Institute (NHGRI), part of the National Institutes of Health (NIH), Wellcome Trust Sanger Institute in Hinxton, England, and the Beijing Genomics Institute, Shenzhen (BGI Shenzhen) in China. Therefore, these genome projects further provide a significant opportunity for market growth in emerging markets.
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·
Predictive & Presymptomatic Testing
·
Prenatal Testing
·
Diagnostic Testing
·
Newborn Screening
·
Others
By Application
·
Oncology
·
Infectious Diseases
·
Autoimmune Disease
·
Others (Rare Disease)
Regional
Analysis
North America
·
United States
·
Canada
Europe
·
UK
·
Germany
·
Spain
·
France
·
Italy
·
Rest of Europe
Asia-Pacific
·
India
·
China
·
Japan
·
Rest oF APAC
Rest of The World
·
Latin
America
·
Middle
East and Africa
Company
Profiles
·
23andMe,
Inc.
·
Abbott
Laboratories
·
Ambry
Genetics Corp, A Konica Minolta Company
·
Blueprint
Genetics Oy
·
bioMérieux
SA
·
BGI
Genomics Co., Ltd.
·
Bio-Rad
Laboratories, Inc.
·
deCODE
genetics
·
Danaher
Corp.
·
Centogene
AG
·
Eurofins
GSC Lux SARL
·
F.
Hoffmann-La Roche Ltd.
·
GeneDx,
Inc.
·
Helix
OpCo LLC
·
Illumina,
Inc.
·
Luminex
Corp.
·
Myriad
Genetics, Inc.
·
NeoGenomics
Laboratories, Inc.
·
PerkinElmer
Inc.
·
Quest
Diagnostics Inc.
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