Long Read Sequencing Market Trends

  • Report ID: 2595
  • Published Date: Jul 28, 2025
  • Report Format: PDF, PPT

Long Read Sequencing Market - Growth Drivers and Challenges

Growth Drivers

  • Technology advancements in genomic analysis: With the growing amount of long read sequencing data, cloud platforms with AI algorithms are becoming crucial in the healthcare sector. The NIH's All of Us program in 2024 initiated a collaboration with Amazon Web Services to host long read genomic datasets for national-scale analysis. AI is now facilitating fast variant annotation, quality scoring, and clinical report generation essential for real-time oncology and infectious disease decision-making. These technologies enhance access, turnaround time, and cost, further increasing demand throughout hospitals and public health labs.
  • Manufacturers' strategies and innovations: Many leading companies are adopting innovative strategies in their firms to broaden long read sequencing footprint. For example, Oxford Nanopore Technologies has collaborated with the UK's National Health Service to deploy LRS in more than 45 regional hospitals in 2024. This move is specially addressed to expand real-time sequencing for cancer patients and infectious diseases. This collaboration has surged the long read sequencing market share by 18.4% in the UK. Similarly, Pacific Biosciences introduced Revio, a 2023 high-throughput LRS platform, reducing per-genome costs by 60.6% and boosting worldwide clinical interest. Strategic partnerships are a major force behind increased adoption and access.
  • Rising patient volume in rare disease genomics: In Europe, long read sequencing of diseases, particularly rare genetic disorders, is growing rapidly. As per the European Organization for Rare Diseases report, in Germany, nearly 1.6 million individuals were living with an undiagnosed rare disease in 2025, up 14.5% over the past decade. Long read sequencing is particularly well adapted for diagnosing diseases with big structural variants, including muscular dystrophy and Huntington's disease. Further, with rising clinical adoption and expanding national genomics initiatives, the patient population for long read applications will increase substantially throughout North America and Europe.

Historical Patient Growth Analysis: Foundation for Future Market Expansion

Historical Patient Growth (2010-2020)

Country

2010 (Patients)

2020 (Patients)

Growth (%)

Comments

USA

220,005

1,570,003

613.9%

Fueled by NIH's All of Us program, and growth in precision oncology labs

Germany

48,008

365,005

660.8%

National rare disease registry and public-private genome initiatives

France

44,004

310,009

604.8%

Genomic medicine initiatives under Inserm and cancer diagnostics programs

Spain

29,010

205,010

607.3%

Ministry of Health genomics expansion via Instituto de Salud Carlos III

Australia

21,009

145,004

590.8%

Genomics Health Futures Mission and rare disease focus

Japan

70,006

480,009

585.9%

AMED-led cancer genome profiling and rare disease programs

India

9,010

122,008

1255.9%

The Government of India’s GenomeIndia and DBT programs catalyzed adoption

China

37,006

670,005

1709.8%

Precision medicine initiative, national biobank investments

Sources: NIH, BMBF, Inserm, HAS, FEDER, Genomics Health Futures Mission, AMED, ICMR, CAS

Manufacturer Strategies Shaping Market Expansion

Revenue Opportunities for Manufacturers

Company Name

Strategy Employed

Revenue Gained ($ Million)

Market Share Growth (%)

Pacific Biosciences (USA)

Revio launch & NIH genomic collaborations

$124.9 million (2023)

+34.7%

Oxford Nanopore (UK)

Adaptive sampling + NHS partnership

$98.4 million (2023)

+28.5%

BGI Genomics (China)

Clinical genomics expansion via MOST

$77.8 million (2023)

+19.3%

Genewiz/Azenta (USA)

Automation upgrades + AHRQ support

$64.2 million (2023)

+16.4%

Nabsys (USA)

Long-read platform optimization

$32.9 million (2023)

+12.5%

Sources: Genome, Genomics England, AHRQ, MOST

Challenges

  • Awareness gaps in genomics sequencing adoption: Nearly 38.5% of U.S. adults were aware of the advantages of genomic sequencing in preventive medicine, according to a 2022 CDC survey. In France and Spain, where there are no early screening programs also the adoption of LRS tools for cancer and rare diseases has also been delayed. Companies like Illumina have introduced awareness campaigns through public hospitals, but their reach remains limited to urban areas. Responding, a number of EU-supported programs, such as the 1.3+ million genomes initiative, are attempting to expand public education and genomic literacy. Moreover, collaborations between biotech companies and national healthcare systems are developing to bring about the integration of long read sequencing into routine diagnostic pipelines.

Base Year

2024

Forecast Year

2025-2037

CAGR

21.6%

Base Year Market Size (2024)

USD 1.6 billion

Forecast Year Market Size (2034)

USD 8.7 billion

Regional Scope

  • North America (U.S., and Canada)
  • Asia Pacific (Japan, China, India, Indonesia, Malaysia, Australia, South Korea, Rest of Asia Pacific)
  • Europe (UK, Germany, France, Italy, Spain, Russia, NORDIC, Rest of Europe)
  • Latin America (Mexico, Argentina, Brazil, Rest of Latin America)
  • Middle East and Africa (Israel, GCC North Africa, South Africa, Rest of the Middle East and Africa)

Browse key industry insights with market data tables & charts from the report:

Frequently Asked Questions (FAQ)

In the year 2025, the industry size of long read sequencing is assessed at USD 1.9 billion.

Long Read Sequencing Market size was over USD 1.6 billion in 2024 and is anticipated to cross USD 8.7 billion by 2034, witnessing more than 21.6% CAGR during the forecast period i.e., between 2025-2034.

North America industry is predicted to dominate majority revenue share of 39.7% by 2037, North America industry is set to dominate majority revenue share of 17.2% by 2034.

The major players in the market are Pacific Biosciences (PacBio), Oxford Nanopore Technologies, Illumina, Inc., BGI Genomics Co., Ltd., Roche Sequencing Solutions, GenapSys, Inc., Strand Life Sciences, Quantapore, Inc., Dovetail Genomics, Nabsys, Inc., Thermo Fisher Scientific, Hitachi High-Tech Corporation, GenXys Health Care Systems, Macrogen, Inc., BaseClear B.V., Biotools Co., Ltd., GenomixLab Sdn. Bhd. and so on.
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