From Discovery
To Clinical Impact

We empower research & clinical innovation with advanced native-read sequencing solutions.

[Who we are]

Wasatch BioLabs, a leading NGS sequencing service provider, harnesses advanced native-read sequencing and streamlined R&D workflows—translating breakthrough discovery into real-world outcomes.

Advancing Research

High-throughput solutions powering academic and translational studies.

[1]

Empowering Biopharma

End-to-end tools for advanced biomarker discovery and development.

[2]

Enhancing Clinical Testing

Scalable sequencing built for precision diagnostics and real-world deployment.

[3]

the Methylation
revolution

Legacy methods like microarrays and bisulfite sequencing lack the resolution and scalability needed for clinical impact, limiting biomarker discovery and slowing adoption in precision health. Wasatch BioLabs’ Direct Whole Methylome (dWMS) platform is a nanopore-based solution optimized through proprietary library preparation and dWMS-specific bioinformatics. By building on the core strengths of Oxford Nanopore Technologies, dWMS delivers high-resolution, end-to-end methylation and variant analysis designed for real-world research and clinical use.

[01]

Native Nanopore Sequencing

Directly detect native methylation—no bisulfite or PCR required.

[02]

Proprietary Library Prep

Increase throughput and read quality, with proprietary protocols.

[03]

CpG + Variant Coverage

Profile methylation and structural variants from a single unified assay.

[04]

Scalable Deployment

Built for multiplexing, cohort studies, and diagnostic-ready workflows.

[05]

Integrated Bioinformatics

Leverage our MethylSeqR tools and expert team for end-to-end support.

[06]

Flexible Assay Design

Tailor coverage depth and protocols to meet your research objectives.

[Our advantages]

Oxford Nanopore Certified Provider

Wasatch BioLabs is the first full-scale clinical lab dedicated to Oxford Nanopore sequencing, offering proprietary platforms like dWMS and standard ONT services for flexible research support.

Direct RNA Sequencing

Profile native RNA with long reads—no reverse transcription required.

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cDNA Sequencing

Resolve full-length isoforms and expression patterns with long reads.

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PCR Amplicon Sequencing

Capture variants and target regions with long-read amplicons.

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Services &
Custom assays

Continue discovering how Wasatch can push your research & impact.