PUBLISHER: Stratistics Market Research Consulting | PRODUCT CODE: 1383304
PUBLISHER: Stratistics Market Research Consulting | PRODUCT CODE: 1383304
According to Stratistics MRC, the Global Genomics Market is accounted for $46.2 billion in 2023 and is expected to reach $118.4 billion by 2030 growing at a CAGR of 14.4% during the forecast period. The study of an organism's whole genome, or collection of genes, is at the center of the scientific discipline known as genomics. All genes, their roles, interactions, and the structure and arrangement of the DNA within an organism are analyzed and characterized. It also has many applications in fields including medicine, agriculture, evolutionary biology, and more. Techniques like DNA sequencing and bioinformatics are frequently used in genomic research to collect and interpret genetic data.
According to the National Cancer Institute, by 2040, the number of new cancer cases is expected to rise by 29.5 million, while cancer-related fatalities will rise by 16.4 million.
Numerous pharmaceutical firms are making growing investments in the study of tailored medicine. With the use of personalized medicine, doctors can pinpoint a patient's precise needs and then prescribe medications and therapies in response. Better healthcare results are ensured by this strategy. Numerous possibilities for market participants will arise as a result of the growth of the customized medicine business.
Gene editing, amplification, sequencing, and multiplexing are just a few of the complicated and delicate techniques used in genomic investigations. These techniques include the use of sophisticated tools, including sequencers, centrifuges, analyzers, liquid handling equipment, and PCR and microarray equipment. Therefore, extreme caution must be used when using all of the devices. Handling such delicate devices is a significant market growth inhibitor.
The prevalence of cancer and the growing use of next-generation sequencing in cancer research are important drivers of the market's expansion. The way cancer is identified and treated is changing as a result of genomics. The methods for detecting cancer from a blood sample are getting better because to genome research. Genomic research has led to a rise in hereditary cancer screening tests. As a result, the market is expanding due to the rising incidence of cancer and the effective use of genomics in cancer diagnosis and treatment.
Despite improvements in DNA sequencing technology, whole genome sequencing and comprehensive genomic profiling are among the most costly genomic tests and analyses. The broad use of genomics in clinical practice is constrained by the high costs involved with genetic testing and interpretation, particularly in locations with limited resources or for people with poor financial means. The availability and accessibility of genomic goods and services are also impacted by financial a factor, which restrains the expansion of the industry.
The early stage of the pandemic saw a little negative rise in the COVID-19 effect. This was caused by a decline in personalized medicine, cancer research, and other research efforts. The epidemic also caused difficulties in delivering post-sales services and the temporary closure of some academic institutions, which disrupted the market as a whole. To examine viral genetic material, laboratories employed the polymerase chain reaction (PCR) and next-generation sequencing (NGS).
The pathway analysis segment is expected to be the largest during the forecast period. One of the most rapidly expanding uses of route analysis is the creation of next-generation therapies. Since the advent of clinical genomics and tailored treatments, pathway-based analysis has drawn increased interest. This is mostly due to the assistance provided by genetics and individualized medicines for the in-depth investigation of the capacity to navigate illness networks and signaling pathways.
The research institutes segment is expected to have the highest CAGR during the forecast period. Researchers with a focus on genomics, financing from public and private foundations, and business partnerships are some of the reasons that contribute to the segment's dominance in the market for genomics services. Additionally, the research institutes category is anticipated to grow faster throughout the projection period due to collaborations with other academic institutions, hospitals, and biotechnology firms.
North America is projected to hold the largest market share during the forecast period due to the support of research institutes and pharmaceutical giants. Due to the effects of genetic expression on human health, genomics is now a crucial component of all illness research and therapeutic development. Additionally, the presence of cutting-edge healthcare infrastructure, which supports the expansion of technical advancements in this industry, and rising demand for biotechnology services in the area are anticipated to support regional growth.
Asia Pacific is projected to hold the highest CAGR over the forecast period due to increased demand for genomics applications in diagnostics and the growing demand for novel therapeutic drugs to fight the increased incidence of diseases. Additionally, the rising incidence of chronic illnesses like cancer, greater government funding for research, and growing consumer awareness all contribute to the expansion of regional markets.
Some of the key players in Genomics market include: BGI Genomics, Myriad Genetics, Inc., Agilent Technologies, Quest Diagnostics Incorporated, Thermo Fisher Scientific, Inc., Eurofins Scientific, Danaher Corporation, Eppendorf AG, Bio-Rad Laboratories, Inc., Color Genomics, Inc., Agilent Technologies, F. Hoffmann-La Roche Ltd., GE Healthcare, Illumina, Inc., Oxford Nanopore Technologies, Quest Diagnostics Incorporated, Pacific Biosciences of California, Inc. and Color Health, Inc.
In June 2023, BGI Genomics was recognized as the GB/T 35770-2022/ISO 37301 Compliance Management System accreditation-approved company, after the extensive evaluation of BSI, a global testing, standardization, and certification authority.
In June 2023, Myriad Genetics and The University of Texas MD Anderson Cancer Center announced their collaboration aimed at metastatic renal cell carcinoma treatment selection and response research and incorporating Myriad's minimal residual disease testing platform based on whole genome sequencing.
In April 2023, Bio-Rad Laboratories, Inc. pivoted their measurable residual disease (MRD) genomics research via a half dozen collaborations with companies and institutions to launch their new QX600™ Droplet Digital™ PCR System.
Note: Tables for North America, Europe, APAC, South America, and Middle East & Africa Regions are also represented in the same manner as above.