Clinical Diagnostic Solutions Leveraging Nanopore Technology

We understand that choosing the right clinical laboratory service provider is a huge decision. This is why we’re committed to providing innovative sequencing technologies with the best customer support, visibility, and experience in the industry.

Whether you’re working at a new startup, an established health system, or on large-scale population-level testing, we have a solution for you. Our proprietary, targeted sequencing technology combined with assays from Oxford Nanopore Technologies and our in-house bioinformatics pipeline allows us to provide the following:

Rapid Turnaround Times

Our automated processing and bioinformatics systems facilitate rapid turnaround times and unprecedented efficiency.

Unrivaled Transparency

Our in-house LIMS gives you and your team direct access to the status of your samples in your portal, keeping you informed at every step of the process.

Streamlined Data Management

Our team of engineers has developed flexible APIs and data delivery platforms to insure our data fits seamlessly into your operations.

Increased Cost Efficiency

Our clients experience, on average, over 20% in cost savings, compared to alternative NGS solutions.

The Process

Convert your current assay to the Nanopore platform

1. Meet with a research specialist to assess the scope and experimental design of your project.

2. We provide your R&D quote and the projected timeline.

‍3. Once the terms are confirmed, your assay is developed.

4. Upon completion, we provide a free run on the platform to provide you with the data for your clinical validation.

Learn More

Person in a lab coat and gloves using a centrifuge.

Case Study Highlight

Inherent Biosciences

"We’ve found that studying and understanding epigenetics is limited by the technology available to investigate DNA methylation. WBL has overcome a lot of these limitations by developing a method of detecting DNA methylation that produces extremely consistent and reliable data between runs. We've been able to identify methylation that was previously obscured by the background noise associated with other NGS platforms.

And it’s not just the increase in methylation visibility. WBL has also outshined our last partner in both time and money—shortening turnaround times down by about 50% and reducing costs by about 20%. In the fertility world, time is extremely precious to our couples, so getting our patients’ data quicker has been invaluable."

Kristen Brogaard

Co-Founder & CEO

Automated Bioinformatics Pipeline For Quick Data Access

Proprietary, in-house bioinformatic pipelines are curated for each type of test that allow us to provide you enhanced data reports and rapid turnaround times. Results are accessible within your WBL portal in .FASTQ formats with qC reports.

Processing

WBL LIMS takes raw sequencing data and processes experiments on a sample-to-sample basis in near-real-time.

Bioinformatics

Proprietary bioinformatic pipelines are curated for each new type of test. These pipelines use machine learning and bioinformatic algorithms to provide novel data and insights.

Security

Because everything is processed in-house, we track and control the data from data genesis to data upload.

R&D

We are always looking at new ways to view and process NGS data and have developed ways to view DNA methylation, determine cell-of-origin, and detect complex diseases.

Data Publication

Our LIMS can organize data according to specific experiments, projects, and samples, making it easier to track and retrieve information. Data is available in raw format or bioinformatic reports.

Integration

Our LIMS API stack is designed to integrate WBL laboratory systems, bioinformatics tools, and databases, enhancing the overall efficiency of the lab. API stack allows data exchange with 3rd party platforms.

Process Integration

Integrating our LIMS with Nanopore instruments and bioinformatics tools streamlines the entire workflow, from sample preparation to data analysis.

Download a custom report here.

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Our Approach

Wasatch BioLabs strives to provide the most accurate, cost-effective DNA & RNA sequencing tools available, placing you at the cutting edge. Our approach is simple—innovative technology, accurate results, fast turnaround times, full transparency, and industry-leading customer and technical support.

‍Consistent Results, Unmatched Support