Rising Prevalence Of Genetic Disorders Fueling The Market Growth Due To Increasing Need For Accurate Mutation Identification: Transformative Forces Shaping the Mutation Detection Kits In Genome Editing Market Landscape in 2025

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What Will the Mutation Detection Kits In Genome Editing Industry Market Size Be by 2025?
The genome editing market's mutation detection kits have seen fast-paced growth in the past few years. The market, which was valued at $1.01 billion in 2024, is expected to increase to $1.14 billion in 2025 at a compound annual growth rate (CAGR) of 13.4%. This significant growth during the historic period can be attributed to a number of factors, including increased genetic disorder research, growing government support for genomics, a rise in academic and clinical research partnerships, the increasing availability of high-tech molecular biology tools, and higher investment levels from biotech firms.

What's the Long-Term Growth Forecast for the Mutation Detection Kits In Genome Editing Market Size Through 2029?
Expect a significant expansion in the mutation detection kits sector of the genome editing market in the forthcoming years, with a projected value of $1.86 billion in 2029, reflecting a compound annual growth rate (CAGR) of 13.1%. This growth over the forecast period can be credited to the increasing use of autonomous mobile robots (AMRs), enhanced focus on supply chain transparency, growing investments in digital twin technologies, amplified demand for immediate asset tracking, and the escalating adoption of industrial automation. The forecast period will also witness major trends such as advancement in real-time location systems (RTLS), the emergence of AI-powered asset tracing, RFID's integration with IoT platforms, the progress in ultra-wideband (UWB) technology, and the incorporation of digital twin solutions in industrial automation.

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What Are the Key Growth Drivers Fueling the Mutation Detection Kits In Genome Editing Market Expansion?
The increased incidence of genetic disorders is anticipated to accelerate the expansion of the mutation detection kits in the genome editing market. Genetic disorders are diseases or conditions resulting from DNA abnormalities, which can be hereditary or arise from novel genetic mutations. Greater awareness and improved diagnostic technologies are fuelling the surge in genetic disorders, leading to early and precise detection and subsequently increased reported prevalence rates. Genome editing mutation detection kits aid in tackling genetic disorders by precisely identifying the genes causing diseases, facilitating concentrated research and the creation of accurate therapeutic interventions. For instance, as stated by the National Health Service, a UK government department, in May 2024, in England, around 17,000 individuals suffer from sickle cell disease, an inherited blood disorder, with approximately 250 new diagnoses each year. Consequently, the escalating incidence of genetic disorders is stimulating the growth of mutation detection kits in the genome editing market.

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What Long-Term Trends Will Define the Future of the Mutation Detection Kits In Genome Editing Market?
Prominent corporations active in the genome editing market for mutation detection kits are prioritizing the creation of cutting-edge products like ultrasensitive multiplexed assays. These are designed to elevate the parameters of precision, swiftness, and sensitivity in detection of genetic mutations. Such advanced diagnostic examinations are capable of identifying multiple genetic mutations at extremely low levels simultaneously. This allows healthcare professionals and scientists to conduct more comprehensive, faster and precise mutation analysis, which subsequently aids in disease diagnosis and tracking treatment progress. In April 2024, for example, Bio-Rad Laboratories Inc., a research firm based in the US, unveiled the ddPLEX ESR1 Mutation Detection Kit. This ultrasensitive multiplexed digital PCR assay was specifically developed for the detection of mutations in breast cancer. The kit can concurrently identify and accurately quantify seven ESR1 mutations, with an analytical sensitivity reaching 0.01% variant allele fraction. It can be applied for both tissue and plasma sample analysis. Innovations like these demonstrate the industry's dedication to upgrading diagnostic precision and facilitating more efficient disease tracking and individualised therapy strategies.

How Is the Mutation Detection Kits In Genome Editing Market Segmented?
The mutation detection kits in genome editing market covered in this report is segmented

1) By Product Type: Reagents, Kits, Software Solutions
2) By Technology: Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR), Transcription Activator-Like Effector Nucleases Or Meganuclease-TAL Effector Nucleases (TALENs/MegaTALs), Zinc Finger Nucleases (ZFN), Other Technologies
3) By Application: Research, Clinical Diagnostics, Drug Development, Other Applications
4) By End Use: Academic Institutions, Hospitals And Diagnostic Centers, Biotechnology Companies

Subsegments:
1) By Reagents: Deoxyribonucleic Acid Polymerases (DNA) Polymerases, Nucleases, Buffers And Enzymes, Fluorescent Dyes And Probes, Primers And Oligonucleotides
2) By Kits: Polymerase Chain Reaction (PCR)-Based Mutation Detection Kits, Next-Generation Sequencing-Based Mutation Analysis Kits, Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) Mutation Validation Kits, Gel Electrophoresis-Based Detection Kits
3) By Software Solutions: Mutation Analysis And Visualization Tools, Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) Off-Target Prediction Software, Genomic Alignment and Annotation Software, Data Interpretation Platforms For Next-Generation Sequencing, Cloud-Based Bioinformatics Platforms

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Which Companies Are Leading the Charge in Mutation Detection Kits In Genome Editing Market Innovation?
Major companies operating in the mutation detection kits in genome editing market are F. Hoffmann-La Roche Ltd, Merck KGaA, Thermo Fisher Scientific Inc., QIAGEN N.V., Eurofins Scientific SE, Agilent Technologies Inc., Illumina Inc., Bio-Rad Laboratories Inc., Integrated DNA Technologies Inc., GenScript Biotech Corporation, Takara Bio Inc., Promega Corporation, Analytik Jena AG, Twist Bioscience Corporation, New England Biolabs Inc., Applied Biological Materials Inc., Synthego Corporation, Cell Signaling Technology Inc., BioVision Inc., Creative Biogene Corporation.

Which Regions Are Leading the Global Mutation Detection Kits In Genome Editing Market in Revenue?
North America was the largest region in the mutation detection kits in genome editing market in 2024. Asia‐Pacific is expected to be the fastest-growing region in the forecast period. The regions covered in the mutation detection kits in genome editing market report are Asia-Pacific, Western Europe, Eastern Europe, North America, South America, Middle East, Africa.

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