RNA-Sequencing (RNA-seq) & Analysis Market to Observe Prominent CAGR of 17.7% by 2030 | Latest Report by Delvens

RNA-Sequencing & Analysis (RNA-seq) Market, By Product and Services (RNA Sequencing Platforms and Consumables, Sample Preparation Products, RNA Sequencing Services, Data Analysis, Storage and Management),Technology (Sequencing By Synthesis, Ion Semiconductor Sequencing, Single-Molecule Real-Time Sequencing, Nanopore Sequencing), Application (Expression Profiling Analysis, Small RNA Sequencing, De Novo Transcriptome Assembly, Variant Calling and Transcriptome Epigenetics), End User (Research and Academia, Hospitals and Clinics, Pharmaceutical and Biotechnology Companies, Other End Users) and region (North America, Europe, Asia-Pacific, Middle East and Africa and South America).

RNA-seq is a widely used technique that provides comprehensive insights into the genomic makeup of an organism or cell. This technique is used in both traditional and non-traditional applications, such as identifying gene expression patterns, detecting mutations, and studying epigenetic modifications. The demand for better sequencing-based diagnostics has led to the development of novel sequencing technologies that can provide more accurate and reliable results. High-throughput sequencers and portable units are two examples of such technologies that have become increasingly popular due to their ability to generate large amounts of data quickly and efficiently.

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The Global RNA-Sequencing & Analysis (RNA-seq) Market size was estimated at USD 2.8 billion in 2022 and is projected to reach USD 8.7 billion in 2030 at a CAGR of 17.7% during the forecast period 2023-2030.

Next-generation sequencing (NGS) technology is a relatively new technology that has gained immense popularity since its launch due to its ability to provide advanced and comprehensive genetic insights. NGS technology is widely used in both traditional and non-traditional applications, such as in research, clinical diagnostics, and personalized medicine, to analyze DNA and RNA sequences. The growing demand for enhanced sequencing-based diagnostics has led to the development of new sequencing technologies that offer improved accuracy, speed, and cost-effectiveness.

RNA sequencing is a technique used to determine the sequence of nucleotides in RNA molecules, which can provide valuable information about the virus's genetic makeup. Single-cell RNA sequencing, stranded RNA sequencing, and ultra-low input RNA sequencing are different methods used to study the virus's features and epidemiology across diverse countries. Single-cell RNA sequencing allows researchers to study individual cells and their gene expression patterns, while stranded RNA sequencing can determine the directionality of RNA molecules. Ultra-low input RNA sequencing is used when only a small amount of RNA is available for analysis.

The prominent players in the RNA-sequencing & analysis (RNA-seq) market are Illumina Inc., Thermo Fischer Scientific Inc., Oxford Nanopore Technologies plc, Agilent Technologies, Inc., BGI, PerkinElmer Inc., QIAGEN, Eurofins Scientific, F. Hoffmann-La Roche Ltd, Takara Bio Inc., GENEWIZ, Inc., Hamilton Company, Macrogen Inc., Zymo Research Corporation, Tecan Trading AG and others.

Recent Developments

In July 2022, Illumina Inc launched Illumina DRAGEN v4.0, an accurate and comprehensive secondary analysis platform.

In January 2021, Oxford Nanopore Technologies collaborated with NVIDIA to integrate the NVIDIA DGX Station A100 into Oxford Nanopore's ultra-high-throughput sequencing system, PromethION.

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Scope of the Report:

The RNA-Sequencing & Analysis (RNA-seq) Market is segmented into various segments such as by Product service, Technology, Application, End-User and Region:

Based on Product service, the RNA-Sequencing & Analysis (RNA-seq) Market is segmented into:

Sample preparation
Application
Method
Sequencing platforms consumables for RNA sequencing
RNA Sequencing Service
Data analysis, storage and management

Based on the Technology, the RNA-Sequencing & Analysis (RNA-seq) Market is segmented into:

Sequencing by synthesis
Ion Semiconductor Sequencing
Single-molecule real-time sequencing
Nanopore sequencing

Based on the Application, the RNA-Sequencing & Analysis (RNA-seq) Market is segmented into:

De Novo Transcriptome Assembly
Expression Profiling Analysis
Variant Calling Transcriptome Epigenetics
Small RNA Sequencing

Based on End-User, the RNA-Sequencing & Analysis (RNA-seq) Market is segmented into:

Research centers and Academic government institutes
Hospital Clinics
Pharmaceutical Biotechnology Companies
Others

Based on Region, the RNA-Sequencing & Analysis (RNA-seq) Market is segmented into:

Asia Pacific

Japan
China
India
Australia
South Korea
Vietnam
New Zealand
Philippines
Thailand
Malaysia
Hong Kong
Taiwan
Singapore
Indonesia
Sri Lanka
Rest of Asia-Pacific

North America

U.S.
Canada
Mexico

Europe

Germany
U.K.
France
Italy
Spain
Sweden
Austria
Finland
Belgium
Turkey
Russia
Poland
Hungary
Czech Republic
Switzerland
Netherlands

Rest of Europe

South America
Brazil
Argentina
Chile
Colombia
Rest of South America

Middle East & Africa

South Africa
U.A.E.
Saudi Arabia
Oman
Qatar
Iran
Egypt
Rest of Middle East and Africa

North America to Dominate the Market

North America dominating the NGS-based RNA-sequencing market due to the increasing initiatives and funds from the government for genomics research.

Asia-Pacific is expected to grow at the highest growth rate in the forecast period of 2022 to 2029 due to the increasing levels of investment for research activities and occurrence of better health facilities.

Next-generation sequencing (NGS) is a high-throughput DNA sequencing technology that has revolutionized the field of genomics. Paired-end (PE) sequencing is a type of NGS that allows for the simultaneous sequencing of both ends of DNA fragments in a library. This technique produces twice as many reads as single-end sequencing, which only sequences one end of the DNA fragment. The forward and reverse reads produced by PE sequencing are aligned as reading pairs, which improves the accuracy of read alignment and enables the detection of insertions and deletions (indels) in the DNA sequence. Indels are important genetic variations that can cause diseases or affect an individual's response to drugs. The ability to detect indels is not achievable with single-read data, which makes PE sequencing a more powerful tool for genomic research. The paired-end strategy is the most modern and well-liked technique among researchers because of its ability to produce high-quality sequencing data and detect genetic variations that are not detectable by other sequencing methods.

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