Genomics Market Trends: Data, Costs, and Clinical Adoption in 2025

Genomics is shifting from research to routine care as sequencing costs plunge and data volumes explode. Market forecasts point to double-digit growth, while cloud and AI reshape pipelines and policy resets recalibrate dealmaking.

Published: November 16, 2025 By Aisha Mohammed Category: Genomics
Genomics Market Trends: Data, Costs, and Clinical Adoption in 2025

A Sector Scaling on Data and Demand

Genomics has moved from a research niche to a core pillar of biomedicine, with investment guided by accelerating data production and clearer clinical use cases. The global genomics market is projected to reach $83.1 billion by 2029 from $46.2 billion in 2024, expanding at a 12.9% CAGR, according to industry analysts at MarketsandMarkets. The growth arc reflects maturing sequencing platforms, richer biobank cohorts, and increasing reimbursement for molecular diagnostics.

Data intensity is rising even faster. Genomics could outpace astronomy and YouTube in raw data generation as whole genomes, single-cell profiles, and spatial maps accumulate at scale, a landmark analysis suggests. Companies such as Illumina, Thermo Fisher Scientific, and Oxford Nanopore Technologies are expanding throughput and automating library prep, effectively turning genomes into a utility input for precision medicine and drug discovery.

Falling Costs, Rising Throughput

Sequencing costs continue their long slide, with the cost to generate a human genome dropping below $1,000 on many platforms; the trend is documented by the U.S. National Human Genome Research Institute’s long-running cost tracking series, NHGRI data show. As capital and reagent efficiency improve, labs are pushing beyond short-read coverage into long-read and hybrid strategies to resolve structural variants and complex regions at scale.

That shift is reshaping platform mixes and pipeline design. Oxford Nanopore’s PromethION line and Illumina’s latest high-throughput instruments anchor competing roadmaps, while Thermo Fisher’s clinical testing footprint supports targeted panels in regulated settings. Startups including DNAnexus and Tempus are building data fabrics atop this hardware layer to standardize pipelines across research and clinical environments. This builds on broader Genomics trends as labs consolidate around interoperable, audit-ready workflows.

From Bench to Bedside: Clinical Adoption and Real-World Evidence

Population-scale genomics is now delivering real-world evidence with clinical utility. The UK Biobank recently completed whole-genome sequencing for its 500,000 participants, unlocking a treasure trove for gene discovery and risk prediction, according to the program...

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