#\Genomics Market Analysis
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Genomics Market Business Growth, Opportunities and Forecast 2024-2030
The global genomics market size was valued at USD 32.65 billion in 2023 and is projected to witness a compound annual growth rate (CAGR) of 16.5% from 2024 to 2030.
The growth of genomics market is attributed to factors such as growing demand for gene therapy, personalized medicine, drug discovery, increasing cancer incidence, and a significant increase in demand for consumer genomics in recent years. Moreover, increasing number of joint ventures and partnerships amongst market players is also expected to have a positive impact on the genomics market growth. For instance, in June 2022, Illumina, Inc., and Allegheny Health Network signed a collaboration for effective evaluation of the impact of in-house Comprehensive Genomic Profiling (CGP) to leverage patient care.
Gather more insights about the market drivers, restrains and growth of the Genomics Market
The COVID-19 pandemic outbreak had posed challenges to applications of genomics technology in terms of research and therapeutics. Nevertheless, some niche applications were of great use to mankind during the pandemic situation to facilitate immediate attention for designing effective diagnostics, effective therapeutics and steps to curb the spread of COVID-19. For example, the viral genome mutational rate (~1-2 bases per month) was gauged for validity of PCR cycle was estimated to understand the efficacy of the re-purposed anti-viral treatments and thereby the vaccine development process was streamlined.
Many genomic surveillance programs were launched country wise to understand the dynamics of pandemic situation and to effective preventive measures. For instance, in December 2020, the Indian SARS-CoV-2 Genomics Consortium (INSACOG) was launched by the joint efforts of Department of Biotechnology (DBT), Ministry of Health, and ICMR with an aim to screen the genomic variations in the SARS-CoV-2 by sequencing technologies. Furthermore, country specific companies are providing consumer genomics services which is also expected to fuel the market size in coming years. One such company being Mapmygenome which is one of the pioneers in India offers DTC genomics services.
The increasing prevalence of inherited cancers is expected create a high demand for cancer genomics. The substantial understanding of human genome have targeted focus on use of various gene therapies for treatment of cancers by modern gene editing techniques such as CRISPR-Cas gene technology. For instance, in September 2022, a group of researchers at the University of California introduced the applications of precision genome editing agents for management of inherited retinal diseases (IRDs).
The development of high-throughput sequencing technologies such as Next-Generation Sequencing (NGS) and microarrays has generated massive amounts of genomic data. However, the rapid accumulation of this data from DNA sequencing and Electronic Health Records (EHRs) poses significant challenges and opportunities for the extraction of biologically or clinically relevant information. Phenome-wide association study (PheWAS) & genome-wide association study (GWAS) are helping researchers to study correlations between genotype and phenotype.
The market players are extensively working towards collaborations, expansions, acquisitions and huge capital investments to advance in research to understand rare diseases and to aid drug discovery. For instance, PacBio declares a collaboration with the Genomics England society for the utility of PacBio’s technology to detect genetic variation in unexplained rare disorders. The study is intended to re-sequence a selection of samples collected during Genomics England’s 100,000 genomes project to discover potential operational and clinical benefits of long-read sequencing for the identification of mutations associated with rare diseases.
Genomics Market Segmentation
Grand View Research has segmented the global genomics market based on application, technology, deliverables, end-use, and region:
Application & Technology Outlook (Revenue, USD Billion, 2018 - 2030)
• Functional Genomics
• Transfection
• Real-Time PCR
• RNA Interference
• Mutational Analysis
• SNP Analysis
• Microarray Analysis
• Epigenomics
• Bisulfite Sequencing
• Chromatin Immunoprecipitation (ChIP & ChIP-Seq)
• Methylated DNA Immunoprecipitation (MeDIP)
• High-Resolution Melt (HRM)
• Chromatin Accessibility Assays
• Microarray Analysis
• Pathway Analysis
• Bead-Based Analysis
• Microarray Analysis
• Real-time PCR
• Proteomics Tools (2-D PAGE; yeast 2-hybrid studies)
• Biomarker Discovery
• Mass Spectrometry
• Real-time PCR
• Microarray Analysis
• Statistical Analysis
• Bioinformatics
• DNA Sequencing
• Others
Technology Outlook (Revenue, USD Billion, 2018 - 2030)
• Sequencing
• PCR
• Flow Cytometry
• Microarrays
• Other technologies
Deliverables Outlook (Revenue, USD Billion, 2018 - 2030)
• Products
o Instruments/Systems/Software
o Consumables & Reagents
• Services
o NGS-based Services
o Core Genomics Services
o Biomarker Translation Services
o Computational Services
o Others
End-use Outlook (Revenue, USD Billion, 2018 - 2030)
• Clinical Research
• Academic & Government Institutes
• Hospitals & Clinics
• Pharmaceutical & Biotechnology Companies
• Other End Users
Regional Outlook (Revenue, USD Billion, 2018 - 2030)
• North America
o U.S.
o Canada
• Europe
o Germany
o U.K.
o France
o Italy
o Spain
o Denmark
o Sweden
o Norway
• Asia Pacific
o China
o India
o Japan
o South Korea
o Australia
o Thailand
• Latin America
o Brazil
o Mexico
o Argentina
• Middle East & Africa
o South Africa
o Saudi Arabia
o UAE
o Kuwait
Browse through Grand View Research's Biotechnology Industry Research Reports.
• The global cell sorting market size was valued at USD 242.7 million in 2023 and is projected to grow at a compound annual growth rate (CAGR) of 8.6% from 2024 to 2030.
• The global live cell imaging market size was valued at USD 2.48 billion in 2023 and is projected to grow at a compound annual growth rate (CAGR) of 9.0% from 2024 to 2030.
Key Companies & Market Share Insights
The market players operating in the genomics market are adopting product approval to increase the reach of their products in the market and improve the availability of their products & services in diverse geographical areas, along with expansion as a strategy to enhance production/research activities. In addition, several market players are acquiring smaller players to strengthen their market position. This strategy enables companies to increase their capabilities, expand their product portfolios, and improve their competencies.
Key Genomics Companies:
• Agilent Technologies
• Bio-Rad Laboratories, Inc.
• BGI Genomics
• Color Genomics, Inc.
• Danaher Corporation
• Eppendorf AG
• Eurofins Scientific
• F. Hoffmann-La Roche Ltd.
• GE Healthcare
• Illumina, Inc.
• Myriad Genetics, Inc.
• Oxford Nanopore Technologies
• Pacific Biosciences of California, Inc.
• QIAGEN N.V.
• Quest Diagnostics Incorporated
• Thermo Fisher Scientific, Inc.
• 23andMe, Inc.
Recent Development
• In November 2023, Fabric Genomics collaborated with DNAnexus and Oxford Nanopore Technologies for deployment of CLIA/CAP labs in pediatric and neonatal ICU’s. The labs will use Oxford Nanopore’s platforms to study genetic disorders in infants.
• In February 2023, Illumina, Inc. entered into a collaboration with African Centre of Excellence for Genomics of Infectious Diseases to start a training institute to increase genomic capabilities in African region
• In January 2023, SOPHiA GENETIC collaborated with the Memorial Sloan Kettering Cancer Center (MSK), a U.S. Cancer Center, to offer researchers and clinicians solutions to expand analytical and testing capabilities.
• In January 2023, Agilent Technologies, Inc. announced acquisition of Avida Biomed, a company that develops target enrichment workflows for clinical researchers utilizing NGS methods to study cancers.
• In April 2022, QIAGEN launched the Biomedical Knowledge Base in Europe, Japan, North America, and Australia to support data science applications in biotech companies
Order a free sample PDF of the Genomics Market Intelligence Study, published by Grand View Research.
#Genomics Market#Genomics Market size#Genomics Market share#Genomics Market analysis#Genomics Industry
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Single-cell Genome Sequencing Market - Forecast(2024 - 2030)
Single-cell Genome Sequencing Market Overview
The Single-cell Genome Sequencing size is estimated to reach $9 billion by 2030, growing at a CAGR of 16.2% during the forecast period 2023-2030. Single-cell genome sequencing is one of the major areas of research for finding a cure for chronic ailments such as cancer. The rising cases of cancer worldwide would drive the Single-cell Genome Sequencing Market during the forecast period. According to Cancer.org, the global burden of new cancer cases would grow to 27.5 million by 2040. This would certainly boost the demand for Single-cell Genome Sequencing Market to find a cure for such chronic diseases.
Rapid development in sequencing technologies is also expected to drive the growth of this market during the forecast period. Polymerase chain reaction (PCR) and next-generation sequencing are emerging as the preferred technologies for various applications, especially for single-cell genomic sequencing. In January 2022, a group of medical Scientists at Stanford and their collaborators developed a new ultra-fast genome sequencing approach that offered a diagnostic rate of about 12% higher than the average rate for diagnosing mystery illnesses.
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Single-cell Genome Sequencing Market - Report Coverage:
The “Single-cell Genome Sequencing Market Report- Forecast (2023-2030)” by IndustryARC, covers an in-depth analysis of the following segments in the Single-cell Genome Sequencing Market.AttributeSegment
By Product Type
Consumables
Reagents
By Technique
Flow Cytometry
Next-generation Sequencing
Polymerase Chain Reaction
Microscopy
Mass Spectrometry
Others
By Application
Cancer
Immunology
Microbiology
Others
By End-User
Academic and Research Laboratories
Hospitals and Diagnostic Centers
Biotechnology and Pharmaceutical Companies
Cell Banks and IVF Centers
By Geography
North America (the U.S., Canada and Mexico)
Europe (Germany, France, the UK, Italy, Spain, Russia and the Rest of Europe),
Asia-Pacific (China, Japan, South Korea, India, Australia & New Zealand and the Rest of Asia-Pacific),
South America (Brazil, Argentina, Chile, Colombia and the Rest of South America)
The Rest of the World (the Middle East and Africa).
COVID-19 / Ukraine Crisis - Impact Analysis:
The COVID-19 pandemic had a positive impact on the Single-cell Genome Sequencing Market. The studies on single-cell genome sequencing offered critical insights into coronavirus infection and allowed medical experts better understand the nature of the infection. On performing single-cell sequencing, most cell types in patients with COVID-19 showed a significant interferon-α response along with an overall acute inflammatory response.
Russia’s invasion of Ukraine has made a significant impact on the Single-cell Genome Sequencing market. It has not only affected the lives and work of genomic researchers in these countries but has also influenced the relationships with colleagues in the U.S. and elsewhere.
The sanctions against Russia are most likely to bring experimental genomics research in the country to a halt. Ukraine had several genomics research projects going on before the war began. Now, with all the unrest, most researchers in Ukraine are fleeing the country and looking for positions in the west.
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Key Takeaways:
Fastest Growth in the Asia-Pacific Region : Geographically, in the global Single-cell Genome Sequencing market share, Asia-Pacific is analyzed to grow with the highest CAGR of 17.2% during the forecast period 2023-2030. This growth is driven by the rising number of cancer cases in the region. According to the projections by the International Agency for Research on Cancer, there would be about 15.1 million new cases per year in Asia until 2040. The unprecedented rate of population aging is the key determinant of this development. Japan, the country with the oldest population in the world, also has the highest rate of cancer. This would drive growth in the Single-cell Genome Sequencing Market in the region during the forecast period.
Reagents Segment to Register the Fastest Growth : In the Single-cell Genome Sequencing analysis, the Reagents segment is estimated to grow with the highest CAGR of 17% during the forecast period. This is because the use of single-cell sequencing reagents allows the experts to process bulk samples with the input of as few as 100 cells. With the recent advancements in single-cell DNA sequencing techniques, bulk DNA sequencing can be done more efficiently and cost-effectively. Moreover, commercial reagents are now available for all the wet-lab steps of a scRNA-seq protocol as well as for preparing barcoded cDNA libraries. The increasing availability of reagents and their growing need in various single-cell genome sequencing processes are boosting its growth in the Single-cell Genome Sequencing Market during the forecast period.
Academic and Research Laboratories Segment is Leading the Market : According to the Single-Cell Genome Sequencing Market forecast, the academic and research laboratories segment held the largest market share of 38.6% in 2022. Single-cell genomics is emerging as one of the major areas in scientific research and development. The rising prevalence of chronic diseases demands new cures and treatment options, which is further boosting the growth of the academic and research laboratories segment. Moreover, understanding the genomics of individual cells opens up a new set of opportunities for the world of biotechnology.
Increased Funding for Vaccine Development and Production : Government agencies in various parts of the world have increased funding for the development and production of vaccines in response to the pandemic. This has led to increased use of single-cell analysis (SCA) tools for COVID-19 research. SCA helps in the assessment of the peripheral immune function of the disease and contributes to the study of the pathophysiology and treatment possibilities of the disease. Thus, the market is positively impacted by COVID-19.
Massive Demand in the field of Immunology, Oncology and Others : Single-cell technology is used in the molecular-level examination of processes and pathways of cellular heterogeneity along with its assessment. This rapidly developing technology has major applications in immunology, oncology and other major areas. Moreover, the development of advanced tools that help make proteomic and transcriptomic processes simpler is also driving the use of single-cell analysis methods, boosting the growth of the Single-cell Genome Sequencing Market.
High Cost of Instruments to Hinder Market Growth : While there is a significant demand for genome sequencing machines among the end-user industries, the instrument costs are significantly high. According to a report published in Bloomberg, Illumina’s new NovaSeq X series costs $985,000 for the base machine and $1.25 million for the advanced one. Such high cost of instruments are likely to hinder the growth of the Single-cell Genome Sequencing Market.
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Key Market Players:
Product/Service launches, approvals, patents and events, acquisitions, partnerships and collaborations are key strategies adopted by players in the Single-Cell Genome Sequencing Market.
The top 10 companies in this industry are listed below:
Standard BioTools Inc. (Maxpar®, Advanta™ Assays)
QIAGEN N.V. (QIAseq FX, REPLI-g)
Illumina, Inc. (NovaSeq, NextSeq)
F. Hoffmann-La Roche AG (AVENIO, MagNA Pure)
Thermo Fisher Scientific, Inc. (Invitrogen, Applied Biosystems)
Bio-Rad Laboratories, Inc. (SEQuoia, ddSEQ)
10X Genomics, Inc. (Chromium, Visium)
Becton, Dickinson and Company (BD Rhapsody™, BD AbSeq)
Oxford Nanopore Technologies Limited (MinION, GridION)
Beijing Genomics Institute Group (CardioGen, COLOTECT™)
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Scope of the Report:
Report MetricDetails
Base Year Considered
2022
Forecast Period
2023–2030
CAGR
16.2%
Market Size in 2030
$9 billion
Segments Covered
Product Type, Technique, Application, End-user and Region
Geographies Covered
North America (the U.S., Canada and Mexico) Europe (Germany, France, the UK, Italy, Spain, Russia and the Rest of Europe),Asia-Pacific (China, Japan, South Korea, India, Australia, New Zealand and the Rest of Asia-Pacific), South America (Brazil, Argentina, Chile, Colombia and Rest of South America) and the Rest of the World (the Middle East and Africa).
Key Market Players
Standard BioTools Inc.
QIAGEN N.V.
Illumina, Inc.
F. Hoffmann-La Roche AG
Thermo Fisher Scientific, Inc.
Bio-Rad Laboratories, Inc.
10X Genomics, Inc.
Becton, Dickinson and Company
Oxford Nanopore Technologies Limited
Beijing Genomics Institute Group
Pacific Biosciences of California, Inc.
NuGEN Technologies, Inc.
Novogene Co. Ltd.
Takara Bio, Inc.
Danaher Corporation
#Single Cell Genome Sequencing Market#Single Cell Genome Sequencing Market Size#Single Cell Genome Sequencing Market Share#Single Cell Genome Sequencing Market Analysis#Single Cell Genome Sequencing Market Revenue#Single Cell Genome Sequencing Market Trends#Single Cell Genome Sequencing Market Growth#Single Cell Genome Sequencing Market Research#Single Cell Genome Sequencing Market Outlook#Single Cell Genome Sequencing Market Forecast
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𝑬𝒎𝒆𝒓𝒈𝒊𝒏𝒈 𝑻𝒓𝒆𝒏𝒅𝒔 𝒊𝒏 𝒕𝒉𝒆 𝑴𝒆𝒕𝒂𝒈𝒆𝒏𝒐𝒎𝒊𝒄𝒔 𝑴𝒂𝒓𝒌𝒆𝒕
𝑺𝒆𝒄𝒖𝒓𝒆 𝑭𝑹𝑬𝑬 𝑺𝒂𝒎𝒑𝒍𝒆: https://www.nextmsc.com/metagenomics-market/request-sample
The 𝑴𝒆𝒕𝒂𝒈𝒆𝒏𝒐𝒎𝒊𝒄𝒔 𝑴𝒂𝒓𝒌𝒆𝒕 is rapidly expanding, driven by advancements in DNA sequencing technologies and a growing focus on understanding microbial communities.
𝑲𝒆𝒚 𝑻𝒓𝒆𝒏𝒅𝒔:
𝑻𝒆𝒄𝒉𝒏𝒐𝒍𝒐𝒈𝒊𝒄𝒂𝒍 𝑨𝒅𝒗𝒂𝒏𝒄𝒆𝒎𝒆𝒏𝒕𝒔: Innovations in sequencing technologies and bioinformatics tools are enhancing the accuracy and efficiency of metagenomic studies.
𝑨𝒑𝒑𝒍𝒊𝒄𝒂𝒕𝒊𝒐𝒏𝒔 𝑨𝒄𝒓𝒐𝒔𝒔 𝑰𝒏𝒅𝒖𝒔𝒕𝒓𝒊𝒆𝒔: From healthcare to agriculture, metagenomics is revolutionizing how we approach disease detection, soil health, and more.
𝑰𝒏𝒄𝒓𝒆𝒂𝒔𝒆𝒅 𝑰𝒏𝒗𝒆𝒔𝒕𝒎𝒆𝒏𝒕: Venture capital and funding are flowing into research and development, fueling the growth of this dynamic market.
𝑾𝒉𝒚 𝑰𝒕 𝑴𝒂𝒕𝒕𝒆𝒓𝒔: Metagenomics offers insights into the microbial world that were previously unattainable, enabling breakthroughs in diagnostics, treatment strategies, and environmental management.
𝑲𝒆𝒚 𝑷𝒍𝒂𝒚𝒆𝒓𝒔: Some of the major players in the market are Agilent Technologies, Inc., F. Hoffmann-La Roche Ltd., Enterome SA, Illumina, Inc., Pacific Biosciences of California, Inc., Oxford Nanopore Technologies Ltd., PerkinElmer, Inc., Swift Biosciences, Inc., Qiagen N.V., Thermo Fisher Scientific, Inc., and many more.
𝑨𝒄𝒄𝒆𝒔𝒔 𝑭𝒖𝒍𝒍 𝑹𝒆𝒑𝒐𝒓𝒕: https://www.nextmsc.com/report/metagenomics-market
As we look ahead, the metagenomics market promises to unlock new possibilities and drive innovation across various sectors. Stay tuned for more updates and insights into this exciting field!
#metagenomics#genomics#innovation#healthcare#biotechnology#market trends#market research#market analysis
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Predictive Genetic Testing & Consumer/Wellness Genomics Market Projections: What to Expect in 2024 and Beyond
Predictive Genetic Testing & Consumer/Wellness Genomics Market Outlook, Scope & Overview:
Industry reports indicate that the global predictive genetic testing & consumer/wellness genomics market was valued at USD 2.2 billion in 2023 and is projected to reach USD 5.10 billion by 2031, growing at a CAGR of 11.1% over the forecast period 2024-2031.
Technological Advancements to Drive Growth of Global Predictive Genetic Testing & Consumer/Wellness Genomics Market
The adoption of predictive genetic testing and consumer/wellness genomics will continue to influence global market revenues. Consumers and healthcare providers are increasingly utilizing these genomic solutions to identify genetic predispositions, personalize healthcare strategies, and enhance overall wellness.
As a product segment, direct-to-consumer (DTC) genetic tests currently hold a significant share of the global predictive genetic testing & consumer/wellness genomics market. This segment is anticipated to grow at a year-over-year rate of 11.1% in 2024 over 2023 and reach USD 5.10 billion in revenues by 2031. The increasing consumer awareness and demand for personalized health and wellness solutions are expected to drive market growth.
Predictive Genetic Testing & Consumer/Wellness Genomics Solutions – Market Dynamics
Drivers:
Predictive genetic testing and consumer/wellness genomics solutions are witnessing significant growth in the global market due to their ability to provide insights into genetic predispositions, inform lifestyle choices, and enable early disease detection. The growing adoption of personalized medicine, the increasing availability of genetic testing services, and advancements in genomic technologies are key factors driving the adoption of these solutions worldwide. Additionally, the rising focus on preventive healthcare and wellness is further propelling market growth.
Restraints:
Despite the growth potential, challenges such as data privacy concerns, ethical issues related to genetic testing, and the high cost of genomic sequencing are hindering the widespread adoption of predictive genetic testing and consumer/wellness genomics solutions. Moreover, the complexity of interpreting genetic data and the need for genetic counseling pose additional challenges to market expansion.
Predictive Genetic Testing & Consumer/Wellness Genomics Solutions – Market Outlook
The proven benefits of predictive genetic testing and consumer/wellness genomics in personalized healthcare, disease prevention, and health optimization have contributed to the market's growth. These solutions are expected to witness increased adoption across major healthcare markets, including North America, Europe, and Asia Pacific, driven by advancements in genomic research and the growing consumer demand for genetic insights.
Global Predictive Genetic Testing & Consumer/Wellness Genomics Market
The rise in demand for predictive genetic testing and consumer/wellness genomics solutions in developed and emerging markets is expected to drive market growth over the forecast period. North America currently holds a significant market share in the global market, with the US being a key contributor to market revenues. Europe and Asia Pacific regions are also experiencing rapid adoption of genomic solutions, supported by favorable regulatory frameworks and increasing investments in genetic research and personalized healthcare.
Key Players in the Predictive Genetic Testing & Consumer/Wellness Genomics Market
Leading companies in the predictive genetic testing & consumer/wellness genomics market include 23andMe, AncestryDNA, MyHeritage, and Helix. These companies are at the forefront of providing advanced genetic testing services for various applications, including ancestry, health risk assessment, and wellness optimization.
In conclusion, the global predictive genetic testing & consumer/wellness genomics market is poised for substantial growth over the forecast period, driven by technological advancements, increasing consumer awareness, and the expanding adoption of personalized healthcare and wellness solutions across diverse settings.
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Artificial Intelligence In Genomics Market May Set New Epic Growth Story
The global Artificial Intelligence In Genomics market focuses on encompassing major statistical evidence for the Artificial Intelligence In Genomics industry as it offers our readers a value addition on guiding them in encountering the obstacles surrounding the market. A comprehensive addition of several factors such as global distribution, manufacturers, market size, and market factors that affect the global contributions are reported in the study. In addition the Artificial Intelligence In Genomics study also shifts its attention with an in-depth competitive landscape, defined growth opportunities, market share coupled with product type and applications, key companies responsible for the production, and utilized strategies are also marked.
Key players in the global Artificial Intelligence In Genomics marketIBM Corporation (United States), Microsoft Corporation (United States), NVIDIA Corporation (United States), Deep Genomics (Canada), BenevolentAI (United Kingdom), Fabric Genomics Inc. (United States), Verge Genomics (United States), Cambridge Cancer Genomics (United Kingdom), Sophia Genetics (United States), Data4Cure Inc. (United States). Free Sample Report + All Related Graphs & Charts @: https://www.advancemarketanalytics.com/sample-report/173521-global-artificial-intelligence-in-genomics-market Although genomic medicine has achieved great advances in recent years, the clinical use of genomics is still evolving as new understanding and technology emerge. One key problem is making sense of exceptionally huge amounts of genomic sequence data and properly integrating and examining it with other relevant information, such as other molecular or clinical data. AI-based computer vision methods are set to change image-based diagnostics in clinical diagnostics, while other AI subtypes have begun to show comparable promise in diverse diagnostic modalities. Deep learning is a sort of AI technique that is used to handle vast and complicated genomic datasets in particular fields, such as clinical genomics.What's Trending in Market:
Rising Adoption of AI in Precision Medicine Segment
Challenges:
Data Theft or Leakage
High Initial Investment
Market Growth Drivers:
High Investments in AI for Genomics
Growth in Healthcare Infrastructure
The Artificial Intelligence In Genomics industry report further exhibits a pattern of analyzing previous data sources gathered from reliable sources and sets a precedent growth trajectory for the Artificial Intelligence In Genomics market. The report also focuses on a comprehensive market revenue streams along with growth patterns, Local reforms, COVID Impact analysis with focused approach on market trends, and the overall growth of the market.Moreover, the Artificial Intelligence In Genomics report describes the market division based on various parameters and attributes that are based on geographical distribution, product types, applications, etc. The market segmentation clarifies further regional distribution for the Artificial Intelligence In Genomics market, business trends, potential revenue sources, and upcoming market opportunities.
Download PDF Sample of Artificial Intelligence In Genomics Market report @ https://www.advancemarketanalytics.com/download-report/173521-global-artificial-intelligence-in-genomics-market The Global Artificial Intelligence In Genomics Market segments and Market Data Break Down are illuminated below: by Application (Diagnostics, Drug Discovery & Development, Precision Medicine, Agriculture & Animal Research, Other), Technology (Deep Learning, Reinforcement Learning, Supervised Learning, Unsupervised Learning, Others), End Use (Hospitals, Specialty Clinics), Functions (Genome Sequencing, Gene Editing, Clinical Workflows, Predictive Genetic Testing), Component (Software, Services (Managed, Professional)) The Artificial Intelligence In Genomics market study further highlights the segmentation of the Artificial Intelligence In Genomics industry on a global distribution. The report focuses on regions of LATAM, North America, Europe, Asia, and the Rest of the World in terms of developing market trends, preferred marketing channels, investment feasibility, long term investments, and business environmental analysis. The Artificial Intelligence In Genomics report also calls attention to investigate product capacity, product price, profit streams, supply to demand ratio, production and market growth rate, and a projected growth forecast.In addition, the Artificial Intelligence In Genomics market study also covers several factors such as market status, key market trends, growth forecast, and growth opportunities. Furthermore, we analyze the challenges faced by the Artificial Intelligence In Genomics market in terms of global and regional basis. The study also encompasses a number of opportunities and emerging trends which are considered by considering their impact on the global scale in acquiring a majority of the market share.The study encompasses a variety of analytical resources such as SWOT analysis and Porters Five Forces analysis coupled with primary and secondary research methodologies. It covers all the bases surrounding the Artificial Intelligence In Genomics industry as it explores the competitive nature of the market complete with a regional analysis.
Brief about Artificial Intelligence In Genomics Market Report with TOC @ https://www.advancemarketanalytics.com/reports/173521-global-artificial-intelligence-in-genomics-market Some Point of Table of Content:Chapter One: Report OverviewChapter Two: Global Market Growth TrendsChapter Three: Value Chain of Artificial Intelligence In Genomics MarketChapter Four: Players ProfilesChapter Five: Global Artificial Intelligence In Genomics Market Analysis by RegionsChapter Six: North America Artificial Intelligence In Genomics Market Analysis by CountriesChapter Seven: Europe Artificial Intelligence In Genomics Market Analysis by CountriesChapter Eight: Asia-Pacific Artificial Intelligence In Genomics Market Analysis by CountriesChapter Nine: Middle East and Africa Artificial Intelligence In Genomics Market Analysis by CountriesChapter Ten: South America Artificial Intelligence In Genomics Market Analysis by CountriesChapter Eleven: Global Artificial Intelligence In Genomics Market Segment by TypesChapter Twelve: Global Artificial Intelligence In Genomics Market Segment by Applications
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#Global Artificial Intelligence In Genomics Market#Artificial Intelligence In Genomics Market Demand#Artificial Intelligence In Genomics Market Trends#Artificial Intelligence In Genomics Market Analysis#Artificial Intelligence In Genomics Market Growth#Artificial Intelligence In Genomics Market Share#Artificial Intelligence In Genomics Market Forecast#Artificial Intelligence In Genomics Market Challenges
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#Spatial Genomics & Transcriptomics Market#Spatial Genomics & Transcriptomics Market size#Spatial Genomics & Transcriptomics Market share#Spatial Genomics & Transcriptomics Market trends#Spatial Genomics & Transcriptomics Market analysis#Spatial Genomics & Transcriptomics Market forecast
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Global Spatial Genomics Transcriptomics Market Is Estimated To Witness High Growth Owing To Increasing Adoption of Spatial Genomics Technologies
Market Overview: Spatial genomics transcriptomics combines the technologies of spatial transcriptomics and genomics to analyze gene expression within the context of tissue architecture. This innovative approach allows researchers to study the spatial organization of gene expression within individual cells, leading to a better understanding of various biological processes and disease mechanisms. The market for spatial genomics transcriptomics is driven by the increasing adoption of these technologies in various research applications, including cancer research, neurobiology, developmental biology, and immunology. The ability to analyze gene expression within the context of tissue architecture provides valuable insights into cell-to-cell interactions, cellular heterogeneity, and spatial relationships, making it a powerful tool for biomedical research. The global Spatial Genomics Transcriptomics Market Size is estimated to be valued at US$ 262.7 million in 2023 and is expected to exhibit a CAGR of 13% over the forecast period 2023-2030, as highlighted in a new report published by Coherent Market Insights. Market Key Trends: One key trend driving the growth of the spatial genomics transcriptomics market is the increasing demand for single-cell analysis. Single-cell analysis allows researchers to study individual cells rather than bulk population samples, providing a deeper understanding of cellular heterogeneity and development. Spatial genomics transcriptomics takes single-cell analysis a step further by incorporating spatial information, enabling researchers to study gene expression within the context of tissue architecture. This integrated approach allows for a more comprehensive analysis of complex biological systems and has the potential to revolutionize our understanding of cellular processes and disease mechanisms. For example, 10x Genomics, one of the key players in the spatial genomics transcriptomics market, offers the Visium Spatial Gene Expression Solution, which enables researchers to analyze gene expression in intact tissue sections. This technology allows for the identification of cell types, mapping of gene expression, and analysis of the spatial relationships between cells. By combining single-cell analysis with spatial information, researchers can gain valuable insights into the role of gene expression in tissue development and disease progression. PEST Analysis: Political: The spatial genomics transcriptomics market is influenced by government regulations and policies regarding genomics research and healthcare. Government funding and support for research initiatives can drive market growth. Economic: The market is driven by increasing investment in genomics research and the growing demand for personalized medicine. The economic factors, such as GDP growth, healthcare expenditure, and disposable income, also impact the adoption of spatial genomics transcriptomics technologies. Social: The growing prevalence of chronic diseases and the need for better diagnostic and treatment options are driving the demand for spatial genomics transcriptomics technologies. The increasing awareness and acceptance of personalized medicine among patients and healthcare professionals are also contributing to market growth. In conclusion, the spatial genomics transcriptomics market is poised for significant growth due to the increasing adoption of these technologies in various research applications. The integration of spatial information with gene expression data provides valuable insights into cellular processes and disease mechanisms, driving the demand for spatial genomics transcriptomics technologies. With advancements in genomics research and technological innovation, this market is set to revolutionize our understanding of biology and contribute to the development of personalized medicine.
#Spatial Genomics Transcriptomics Market#Spatial Genomics Transcriptomics Market Size#Coherent Market Insights#Spatial Genomics Transcriptomics Market Demand#Spatial Genomics Transcriptomics Market Growth#Spatial Genomics Transcriptomics Market Trends#Spatial Genomics Transcriptomics Market Analysis#Spatial Genomics Transcriptomics Market Forecast
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The Global Genomic Data Analysis & Interpretation Market is likely to grow at a CAGR of around 11.10% during the forecast period, i.e., 2022-27, says MarkNtel Advisors. The market growth attributes principally to the burgeoning cancer cases worldwide, encouraging numerous biotechnology companies to develop genomic software solutions for data analysis to help clinicians provide precision oncology treatments.
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Genomic Data Analysis and Interpretation Market Research Report 2022 to 2028: Industry Trends, Regional Wise Outlook, Growth Projections and Opportunities
This report provides a comprehensive analysis of current Global Genomic Data Analysis and Interpretation Market based on segmented types and downstream applications. Major product development trends are discussed under major downstream segment scenario.This report also focuses on major driving factors and inhibitors that affect the market and competitive landscape. Global and regional leading players in the Genomic Data Analysis and Interpretation industry are profiled in a detailed way, with sales data and market share info. This report also includes global and regional market size and forecast, drill-down to top 20 economies.
According to this survey, the global Genomic Data Analysis and Interpretation market is estimated to have reached $ xx million in 2020, and projected to grow at a CAGR of xx% to $ xx million by 2028.
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Covid-19 pandemic has impacted the supply and demand status for many industries along the supply chain. Global Genomic Data Analysis and Interpretation Market Status and Forecast 2022-2028 report makes a brilliant attempt to unveil key opportunities available in the global Genomic Data Analysis and Interpretation market under the covid-19 impact to help readers in achieving a better market position. No matter the client is industry insider, potential entrant or investor, the report will provide useful data and information.
The Global Genomic Data Analysis and Interpretation Market has been exhibited in detail in the following chapters
Chapter 1 displays the basic product introduction and market overview.
Chapter 2 provides the competition landscape of global Genomic Data Analysis and Interpretation industry.
Chapter 3 provides the market analysis by type and by region
Chapter 4 provides the market analysis by application and by region
Segmented by Type
l Next-Generation Sequencing (NGS)
l Polymerase Chain Reaction (PCR)
l Microarray
l Other Genomic Platforms
Segmented by Application
l Research and Academic Institutions
l Biotechnology and Biopharmaceutical Companies
l Hospitals and Diagnostic Laboratories
l Contract Research Organizations
l Forensic Laboratories
l Other End Users
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Segmented by Country
North America
United States
Canada
Mexico
Europe
Germany
France
UK
Italy
Russia
Spain
Asia Pacific
China
Japan
Korea
Southeast Asia
India
Australasia
Central & South America
Brazil
Argentina
Colombia
Middle East & Africa
Iran
Israel
Turkey
South Africa
Saudi Arabia
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Key manufacturers included in this survey
l Thermo Fisher Scientific Inc.
l SoftGenetics LLC
l QIAGEN N.V.
l Partek
l Pacific Biosciences of California
l Oxford Nanopore Technologies
l Illumina
l Golden Helix
l Genomics
l F. Hoffmann-La Roche Ltd
l DNASTAR
l Bio-Rad Laboratories
l Beijing Genomics Institute (BGI)
l ASURAGEN INC
l Agilent Technologies
l 10x Genomics
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Genomics Market - Forecast(2024 - 2030)
Global Genomic Market Overview:
A genome is the genetic material of an organism. It includes both the genes and the noncoding DNA, as well as mitochondrial DNA and chloroplast DNA. The study of genomes is called genomics. The genomics market is gaining traction owing to its applications in various fields of study such as intragenomic phenomenon including epistasis, pleiotropy, heterosis, and other interactions between loci and alleles within the genome. In this era of medical and life science innovations shaping itself as an inevitable uptake for sustainability of mankind, the genomic research is poised for exponential growth owing to imperative genetic innovations feeding off it. Abundant potential has driven this arcade to reach a staggering market size of $16 billion - $16.5 billion as of 2018, and the demand is estimated to increment at formidable CAGR of 9.2% to 10.2% during the forecast period of 2019 to 2025.
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Global Genomic Market Outlook:
Genomics is extensively employed in healthcare, agriculture, biotechnology, DNA sequencing, and diagnostics. In the healthcare segment, genomics is used for the development of vaccines and drugs. This segment leads the application vertical and is growing with a CAGR of 10.1%-10.7 % through to 2025. Genomics plays a significant part in diagnosis of several genetic disorders. It has an ample scope in personalized medication as it can advocate a medical management constructed on the genetic face of a person with the help of clinical data and AI. It is also applied in synthetic biology and bioengineering. Genomics research in agriculture is hired for plant breeding and genetics to cultivate crop production. The understanding of gene function and the accessibility of genomic maps along with an enhanced understanding of genetic variant will aid the plant breeders to identify the traits and then manipulate those traits to obtain a high yield. All these factors affecting the enormous medical and agricultural sector are all set to stroke the genomics market with abundant demand.
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Global Genomic Market Growth Drivers:
As per the National Center for Biotechnology Information, U.S, the progression in oncology (study and treatment of tumor) expenses is forecast to rise 7%–10% annually throughout 2020, with universal oncology cost exceeding $150 billion[1]. As per the WHO, cancer is a leading cause of death worldwide, accounting for an estimated 9.6 million deaths in 2018[2]. And the total annual economic cost of cancer at the initial period of this decade was estimated at approximately $1.16 trillion. Thus the application of genomics in exploring cell-free circulating DNA by several R&D sectors as a potential biomarker for cancers is driving the market towards exponential growth. The genomics market with its current potential displays all the necessary traits it can adapt in the coming years to divert a huge chunk of traffic and revenue from the omnipresent cancer diagnostics.
As per the Food and Agriculture Organization of United Nations, between 1960 and 1990 the arable land increased by 1.5 billion ha, and in the recent past decades the elevation recorded is just 155 million ha[3]. With decreasing arable floor and the increasing global population augmenting the demand for food by 70% (by 2050), obtaining a high yield is a major trend in the agricultural sector. Genomics market is all set to capitalize on this unprecedented demand scenario. Genomics supplements the understanding of gene function and the accessibility of genomic maps along with an enhanced understanding of genetic variant, thus aiding the plant breeders to identify the traits and then manipulate those traits to obtain a high yield.
After an acute analysis of the regional insights of the global genomics market, North America is revealed to hold 39% to 40% of the entire global market size as of 2018. Such dominance can be attributed to several aspects such as cumulative investment on research by federal administrations, growing patient awareness, and accessibility of urbane healthcare facilities.
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Global Genomics Market Players Perspective:
Some of other key players profiled in this IndustryARC business intelligence report are Beckton Dickson, Synthetic Genomics Inc. (SGI) ,Cepheid, Inc., Affymetrix, Inc., Bio-Rad Laboratories, Inc., Agilent Technologies, GE Healthcare, Illumina, Inc., Danaher Corporation,F. Hoffmann-La Roche, QIAGEN, Thermo Fisher Scientific and PacBio (Pacific Biosciences of California). Majority of the companies mentioned are situated in North America augmenting the regional affluence in the global market.
Global Genomics Market Trends:
High overload owing to a wide range of reagents and consumables has propelled companies into approving different policies to endure in the market and stay ahead of the curve.
For instance, in January 2017, BD launched Precise WTA Reagents for precise and guileless quantification of hereditary data form single cell analysis. Moreover, in July 2016, SGI-DNA entered into a distribution agreement with VWR International, an American company involved in the distribution of research laboratory products, with over 1,200,000 items to more than 250,000 customers in North America and Europe.
Genomics Market Research Scope
The base year of the study is 2018, with forecast done up to 2025. The study presents a thorough analysis of the competitive landscape, taking into account the market shares of the leading companies. It also provides information on unit shipments. These provide the key market participants with the necessary business intelligence and help them understand the future of the Genomics Market. The assessment includes the forecast, an overview of the competitive structure, the market shares of the competitors, as well as the market trends, market demands, market drivers, market challenges, and product analysis. The market drivers and restraints have been assessed to fathom their impact over the forecast period. This report further identifies the key opportunities for growth while also detailing the key challenges and possible threats. The key areas of focus include the types of equipment in the Genomics Market, and their specific applications in different phases of industrial operations.
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Genomics Market Report: Industry Coverage
Types of Solutions Genomics Market:
By Product Types- Microarray chip, Sequencers.
By Application- Genotyping, SNP analysis.
By End-User- Anthropology, Diagnostics.
The Genomics Market report also analyzes the major geographic regions for the market as well as the major countries for the market in these regions. The regions and countries covered in the study include:
North America: The U.S., Canada, Mexico
South America: Brazil, Venezuela, Argentina, Ecuador, Peru, Colombia, Costa Rica
Europe: The U.K., Germany, Italy, France, The Netherlands, Belgium, Spain, Denmark
APAC: China, Japan, Australia, South Korea, India, Taiwan, Malaysia, Hong Kong
Middle East and Africa: Israel, South Africa, Saudi Arabia
#genomics#genomics market#genomics market size#genomics market share#genomics market value#genomics market report#DNA microarrays#Electrophoresis#X-Ray Crystallography#Polymerase Chain Reaction#DNA Sequencers#Chromatography#Bio-informatics Tools#Bio-informatics Database#DNA Sample Sequencing#SNPS Analysis#Molecular Biology#Gene Expression Analysis#Genotyping#Targeted Re-sequencing#Individual Genome Sequencing#Biomarker Solutions
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Analysis, Theories & Background Information On:
This thing
Smeech!
Smeech is a Yordle chem-baron and the boss of the Scrap Hackers.
Based on his appearance alone (the only features really shown are his face, torso and hands), Smeech is a cyborg.
While Smeech doesn’t necessarily look tall based on the small appearances in the show, Smeech is most likely around 5’6 to 5’7. As stated in his wiki page, Smeech has mechanical limbs attached to his hands and feet to make himself as tall as a normal human.
While there isn’t much to Smeech’s character, it’s stated that his origin region is Bandle City.
Because Smeech is a Yordle (like Heimerdinger), perhaps is also nearly 400? Maybe around that number.
More depth/Background + Theories within:
According to Smeech’s wiki page, Smeech’s business as the boss of the Scrap Hackers involved with a lot of technology and mainly cyborgs within his organization. A common theme in Silco’s business are Cyborgs (such as Finn, Smeech and (not entirely) Sevika). Perhaps because of this, Finn and Smeech make business deals or just generally hang out?
Speaking of Finn and Smeech, it also seems that Smeech and Finn are close coworkers (especially considering Smeech was involved in the discussion.)
In the first (and most likely final) scene where Smeech is seen, Smeech also seems to be a character who is easy to ‘be placed in line’, such as how Smeech immediately backed down from Finn’s offer after Silco planned the gas attack.
Also, based on his appearance (and this is just a theory), perhaps Smeech was experimented on with Shimmer like Deckard was (based on how battered and frail Smeech looks, along with his eyes being a similar color to Jinx’s in the last episode).
Smeech also advertises his company; “The Scrap Hackers provide body augments to anyone willing to pay the price, both physically and monetarily. From genome hacking to mech-exoskeleton construction, we make the impossible possible. Whether you’re in the market for purely cosmetic enhancements or modifications to augment strength, speed and agility - we have the technology to make your bio-dreams a reality.”
According to Smeech’s wiki page, Smeech isn’t one to be messed with, especially if it means someone isn’t paying their debt. In his wiki, it states that he had a problem with someone in the lanes, so he “sent him a signed note and a warning to not go to his compatriots and made a joke about the man's amputated leg. He then had his henchman break into the man's warehouse to go through the man's things and presumably steal what was believed by the investigators to be a stash of medical equipment. Because the target confronted his docile but strong lackey, the man was killed, with part of the encounter seen by a witness, and became the subject of a homicide investigation.”
#arcane#mircon rambles#sevika mentioned#smeech arcane#smeech#silco mentioned#Finn mentioned#jinx mentioned#shimmer mentioned#arcane theory#arcane analysis#arcane character analysis#I like talking about background characters :]
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Artificial Intelligence In Genomics Market Forecast: What to Expect in the Coming Years
Artificial Intelligence in Genomics Market Outlook, Scope & Overview:
Industry reports indicate that the global artificial intelligence in genomics market was valued at USD 726.9 million in 2023 and is projected to reach USD 15,007.1 million by 2031, growing at a CAGR of 46.0% over the forecast period 2024-2031.
Technological Advancements to Drive Growth of Global Artificial Intelligence in Genomics Market
The adoption of advanced AI technologies in genomics will continue to influence global market revenues. Researchers and healthcare professionals are increasingly utilizing AI for genomics due to its ability to analyze large datasets and provide precise insights for genetic research and personalized medicine.
As a technology segment, machine learning algorithms currently hold a significant share of the global AI in genomics market. This segment is anticipated to grow rapidly at a year-over-year rate, driven by the increasing need for advanced data analysis tools in genomics research.
AI in Genomics – Market Dynamics
Drivers:
Artificial intelligence is transforming the genomics field by enhancing data analysis capabilities and enabling more accurate and faster genetic sequencing. The integration of AI in genomics helps in identifying genetic mutations, understanding gene functions, and predicting disease susceptibility. The increasing investments in AI and genomics research, along with the growing demand for personalized medicine, are key factors driving the growth of this market.
Restraints:
Despite the promising growth, the high cost of implementing AI technologies in genomics and the need for skilled professionals to operate advanced AI systems pose significant challenges. Additionally, concerns regarding data privacy and security in handling sensitive genetic information may hinder the widespread adoption of AI in genomics.
AI in Genomics – Market Outlook
The effective outcomes from the use of AI in genomics in enhancing research capabilities and advancing personalized medicine have boosted the prominence of this technology in the global market. AI in genomics is expected to witness significant growth, particularly in regions with strong research infrastructure and supportive regulatory environments.
Global AI in Genomics Market
The upsurge in the application of AI in genomics in North America, Europe, and Asia Pacific is expected to drive market growth over the forecast period. North America currently holds a significant market share in the global AI in genomics market, with the US being a key contributor to market revenues. Europe and Asia Pacific regions are also experiencing a surge in AI applications in genomics, driven by advancements in AI technologies and increasing research funding.
Key Players in the AI in Genomics Market
Leading companies in the AI in genomics market include IBM Watson Health, NVIDIA Corporation, Google AI, Deep Genomics, and Illumina Inc. These companies are at the forefront of integrating AI with genomics, offering innovative solutions for genetic research and personalized healthcare.
In conclusion, the global artificial intelligence in genomics market is poised for explosive growth over the forecast period, driven by technological advancements, increasing research investments, and the growing need for personalized medical solutions.
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#Artificial Intelligence In Genomics Market#Artificial Intelligence In Genomics Market Size#Artificial Intelligence In Genomics Market Share#Artificial Intelligence In Genomics Market Trends#Artificial Intelligence In Genomics Market Growth#Artificial Intelligence In Genomics Market Analysis#Artificial Intelligence In Genomics Market Outlook
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How Artificial Intelligence can both benefit us and affect humans?
The evolution of artificial intelligence (AI) brings both significant benefits and notable challenges to society.
And my opinion about artificial intelligence is that can benefit us but in a certain way it can also affect us.
And you will say why I think that is good because mainly it is because several aspects are going to change and for some things the help you give us will be useful but for other things it is going to screw us up very well.
And now I'm going to tell you some Advantages and some Disadvantages of AI
Benefits:
1. Automation and Efficiency: AI automates repetitive tasks, increasing productivity and freeing humans to focus on more complex and creative work. This is evident in manufacturing, customer service, and data analysis.
2. Healthcare Improvements: AI enhances diagnostics, personalizes treatment plans, and aids in drug discovery. For example, AI algorithms can detect diseases like cancer from medical images with high accuracy.
3. Enhanced Decision Making: AI systems analyze large datasets to provide insights and predictions, supporting better decision-making in sectors such as finance, marketing, and logistics.
4. Personalization: AI personalizes user experiences in areas like online shopping, streaming services, and digital advertising, improving customer satisfaction and engagement.
5. Scientific Research: AI accelerates research and development by identifying patterns and making predictions that can lead to new discoveries in fields like genomics, climate science, and physics.
Challenges:
1. Job Displacement: Automation can lead to job loss in sectors where AI can perform tasks traditionally done by humans, leading to economic and social challenges.
2. Bias and Fairness: AI systems can perpetuate and amplify existing biases if they are trained on biased data, leading to unfair outcomes in areas like hiring, law enforcement, and lending.
3. Privacy Concerns: The use of AI in data collection and analysis raises significant privacy issues, as vast amounts of personal information can be gathered and potentially misused.
4. Security Risks: AI can be used maliciously, for instance, in creating deepfakes or automating cyberattacks, posing new security threats that are difficult to combat.
5. Ethical Dilemmas: The deployment of AI in critical areas like autonomous vehicles and military applications raises ethical questions about accountability and the potential for unintended consequences.
Overall, while the evolution of AI offers numerous advantages that can enhance our lives and drive progress, it also requires careful consideration and management of its potential risks and ethical implications. Society must navigate these complexities to ensure AI development benefits humanity as a whole.
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World’s largest epilepsy study reveals ‘genetic architecture’ and points to new therapies
- By Luciana Constantino , Agência FAPESP -
Considered the largest genetic study of epilepsy in the world, a study published in the journal Nature Genetics reveals specific alterations in DNA that signal a greater risk of the brain disorder.
Identifying these alterations will improve diagnosis and advance the possibility of new treatments for the disease.
The researchers identified 26 different areas (loci) of the genome that are linked to epilepsy, with 29 genes thought to play an important role in the disorder. Of these genes, 17 were associated with epilepsy for the first time; ten are linked to the development of the disease when mutated or altered (known as monogenic epilepsy genes) and the other seven are known to already have approved drugs that focus on treating autism spectrum disorders.
Analysis of the subtypes revealed significantly different “genetic architectures” mainly between two subtypes of epilepsy – focal and generalized – and common variations in DNA can explain between 39.6% and 90% of the genetic risk for the latter type.
Coordinated by a consortium of the International League Against Epilepsy (ILAE) involving more than 350 scientists, the study compared data from 29,944 people with the disease to those of 52,538 control subjects. It included epilepsy cases of European (92%), African (3%) and Asian (5%) descent.
Brazil was the only Latin American representative through the Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), a FAPESP Research, Innovation and Dissemination Center (RIDC) based at the State University of Campinas (UNICAMP).
“We at BRAINN were involved in all stages of the work, from the detailed characterization of the patients from a clinical, imaging and neurophysiological point of view – which we’re very good at – to planning the analyses, suggesting how they could be carried out and then checking the results. We were also actively involved in writing the article, which was submitted to the journal over a year ago. Many international studies exclude patients from Brazil because we have such great genomic diversity. However this study did a meta-analysis, which allows us to combine populations with different genomic structures. For the future, we want to expand this diversity even more,” Iscia Teresinha Lopes-Cendes, a professor at UNICAMP’s School of Medical Sciences and co-author of the BRAINN article, told Agência FAPESP.
There are an estimated 2 million Brazilians with epilepsy, at least 25% of whom are uncontrolled, according to the Ministry of Health. Worldwide, the World Health Organization (WHO) estimates that 50 million people are affected by the disorder, a third of whom are resistant to the treatments available on the market.
A highly hereditary neurological disease with no cure, epilepsy causes seizures, up to 40 or 50 a day in the most severe cases, leading to loss of consciousness and falls. Uncontrolled seizures not only disrupt the patient’s daily routine but also pose a serious risk of sudden and premature death.
Treatment involves a combination of medications, which are not always effective. Most medications reduce the activity of neurons across the board, which controls seizures, but they have side effects. An alternative is surgery to remove the part of the brain affected by the malformation.
Now, the researchers are proposing some medications that are normally used for other conditions, but act on the epilepsy risk genes identified in the study.
Knowledge over time
Recognizing the complexity of the genetic and environmental factors related to epilepsy, the consortium was formed in 2010 to collaborate on investigating large datasets at an international level.
“This is an important milestone for the ILAE Consortium on Complex Epilepsies and shows what can be achieved when scientists collaborate openly and share data from around the world,” said the league’s president, Professor Helen Cross, in a press release.
To arrive at the results suggesting different genetic architectures between focal and generalized forms of epilepsy, genetic data were combined with databases of phenotypic information, expanding the sample to more than 51,600 patients and 1 million “controls.” This discovery of the different genetic framework for the different types of epilepsy provides clues to understanding the various syndromes.
In their work, the scientists point out that the proteins that carry electrical impulses through the gaps between the brain’s neurons are part of the risk for generalized forms of epilepsy. In this sense, they emphasize the importance of accurately characterizing or classifying specific epileptic syndromes (syndromic phenotyping) in order to better understand the genetic basis of the disease.
An advocate of studies with so-called “pure data,” Lopes-Cendes says that she is now working specifically on mesial temporal lobe epilepsy (MTLE) with hippocampal atrophy. “We’ve been continuously generating data for specific research on the topic. I’d argue that in certain studies, mixing information from different types of epilepsy can ’dilute’ the data and not highlight results that might appear if the group of patients studied was more homogeneous. I think a balance is needed,” she adds.
In early 2023, the researcher and her group published another article that deepened our understanding of MTLE, considered the most common and refractory to pharmacological treatment, by evaluating, for the first time, the profile of messenger RNA (mRNA, a molecule that contains the information for the production of proteins) from surgical tissue obtained from patients.
Because of her work in genetics, Lopes-Cendes was recently invited by the WHO to join the new Technical Advisory Group on Genomics (TAG-G), which is responsible for contributing to the process of accelerating access to genomic knowledge and technologies, especially in low- and middle-income countries. The group consists of 15 scientists from different countries.
The article “GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture” can be read at: www.nature.com/articles/s41588-023-01485-w.
This text was originally published by FAPESP Agency according to Creative Commons license CC-BY-NC-ND. Read the original here.
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For epilepsy sufferers, cutting-edge technology offers early alerts of seizures
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Magnetic Beads Market Outlook: World Approaching Demand & Growth Prospect 2022-2027
Global Magnetic Beads Market Report from AMA Research highlights deep analysis on market characteristics, sizing, estimates and growth by segmentation, regional breakdowns & country along with competitive landscape, players market shares, and strategies that are key in the market. The exploration provides a 360° view and insights, highlighting major outcomes of the industry. These insights help the business decision-makers to formulate better business plans and make informed decisions to improved profitability. In addition, the study helps venture or private players in understanding the companies in more detail to make better informed decisions.
Major Players in This Report Include Thermo Fisher Scientific Inc (United States),Merck KGaA, Darmstadt (Germany),Polysciences, Inc. (United States),Qiagen (Germany),MagQu Co. Ltd. (Taiwan),FUJIFILM Wako Pure Chemical Corporation (Japan),Takara Bio Inc. (Japan),Spherotech Inc (United States),Cube Biotech GmbH (Germany),Lab on a Bead AB (Sweden)
Magnetic beads & particles are used as carriers of antibodies, antigens, catalyzers, proteins as well as nucleic acids, allowing action on viruses, cells, bacteria, & other biological entities. Magnetic beads are an ultimate tool for immobilizing molecules such as proteins or nucleic acids on a solid phase. They can be additionally used in many applications. This magnetic bead separation process is an efficient, rapid, clean which many scientists are using to substitute centrifugation, filtration, as well as separation techniques. These are used for immunoprecipitation applications. These ensure the rapid & reproducible isolation of proteins. Market Drivers Growing Number of Life Sciences Research Activities
Rising Need to Identify Antigens That Are Related With Autoimmune Diseases
High Demand in The Biopharmaceuticals Field Involving The Application, Opportunities For New Innovation in The Field of Life Science
Opportunities Growing Genomics & Proteomics Research with the Increasing Adoption of Immunoprecipitation in the Coming Years
Growing Funding for Cell Based R&D by Government and Biotechnology companies
Challenges Quality Concerns over Research Antibodies
The Magnetic Beads market study is being classified by Application (Human Cell Separation, Animal cell separation (clinical study), Secondary cell separation), End Users (Healthcare Facilities (Hospitals, Clinics, and Others), Individual Pathology Labs, Research Institutes, Others), Magnetic Beads Size (Small beads (1-10 µm), Medium beads (20-40 µm), Large beads (70-120 µm)), Isolation Technique (Positive, Negative, Others (Depletion, and Others)) Presented By
AMA Research & Media LLP
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Genomics Market Expected To Witness High Growth Driven By Advancements In Technology And Rising Demand For Personalized Medicine
A) Market Overview:
Genomics is the study of genes and their functions, with a focus on understanding the structure, function, evolution, mapping, and editing of genomes. It plays a crucial role in personalized medicine, drug discovery, and the development of precision therapies. The market mainly consists of products such as instruments & consumables, services, and software used in genomic research and diagnostics.
The global Genomics Market is estimated to be valued at US$ 46.2 Bn in 2023 and is expected to exhibit a CAGR of 12.4% over the forecast period 2023-2028, as highlighted in a new report published by Coherent Market Insights.
B) Market Dynamics:
The global Genomics Market is driven by two major factors. Firstly, advancements in technology have revolutionized genomics research and diagnostics. The development of Next-Generation Sequencing (NGS) technologies and its applications in various genomic studies have significantly contributed to market growth. NGS enables faster and cost-effective sequencing of DNA, RNA, and proteins, thereby facilitating a deeper understanding of diseases at a molecular level.
Secondly, there is a rising demand for personalized medicine, which utilizes genomic information to tailor medical treatments to individual patients. The increasing prevalence of chronic diseases such as cancer and genetic disorders has created a need for more targeted therapies. Genomic testing enables the identification of specific genetic mutations associated with these diseases, allowing for personalized treatment plans.
C) Market Key Trends:
One key trend observed in the Genomics Market is the growing adoption of direct-to-consumer genetic testing. Companies such as 23andMe provide consumers with the opportunity to access their genetic information through at-home testing kits. This trend has gained popularity due to increased consumer awareness and curiosity about their DNA and ancestry.
For example, 23andMe offers ancestry reports, health predisposition reports, and carrier status reports, providing individuals with insights into their genetic background and potential health risks. This trend is expected to continue, as more people are interested in exploring their genetic information for various purposes.
D) SWOT Analysis:
Strength:
1. Advancements in technology - Continued advancements in genomic technologies such as NGS drive the market's growth.
2. Increasing demand for personalized medicine - The rising prevalence of chronic diseases and genetic disorders fuels the adoption of genomic approaches in clinical decision-making.
Weakness:
1. High costs associated with genomic testing - The cost of genomic tests and sequencing technologies may limit their accessibility, hindering market growth.
2. Regulatory challenges - Stringent regulations regarding the use and sharing of genetic data pose challenges for the market expansion.
Opportunity:
1. Growing applications in non-invasive prenatal testing - Genomics has the potential to revolutionize prenatal care by enabling non-invasive detection of fetal genetic abnormalities.
2. Expanding use of genomics in agriculture - The agricultural sector can benefit from genomics-based technologies for crop improvement and disease resistance.
Threats:
1. Ethical and privacy concerns - The collection and utilization of genetic data raise ethical questions and privacy concerns among individuals and regulatory bodies.
2. Lack of awareness and limited infrastructure - Limited awareness about genomics and inadequate infrastructure in certain regions can hinder market growth.
E) Key Takeaways:
- The global genomics market is expected to witness high growth, exhibiting a CAGR of 12.4% over the forecast period, driven by advancements in technology and rising demand for personalized medicine.
- North America is currently the largest market for genomics, owing to the presence of well-established healthcare infrastructure, increased funding for genomics research, and a growing consumer base for direct-to-consumer genetic testing.
- Key players operating in the global genomics market include Thermo Fisher Scientific, Agilent Technologies, Bio-Rad Laboratories, Illumina, Pacific Biosciences, Oxford Nanopore Technologies, 23andMe, Foundation Medicine, Hoffmann-La Roche Ltd., and Myriad Genetics Inc. These players focus on product development, partnerships, and acquisitions to maintain their market position and enhance their product offerings.
#Genomics Market#Coherent Market Insights#Genomics Market Demand#Genomics Market Growth#Genomics Market Sale#Genomics Market Trends#\Genomics Market Analysis
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