Leverage the utility of genome sequencing automation
Our liquid handling includes cDNA synthesis, amplification of targets, indexing, nucleic acid clean-up, and initiating the sequencing run with no manual library preparation required.
A fully automated, next-generation sequencing platform that offers complete characterization of select pathogens. Built to deliver accurate and near real-time results, Clear Dx™ is revolutionizing the way clinical and public health labs approach genomic and pathogen surveillance.
Our fully automated sequencing platform helps you work quickly and efficiently—offering you the agility to address pathogen outbreaks and more productive time to perform other lab tasks.
Our liquid handling includes cDNA synthesis, amplification of targets, indexing, nucleic acid clean-up, and initiating the sequencing run with no manual library preparation required.
Clear Dx™ reduces hands-on time from 9 hours to less than 45 minutes, cuts down the number of human touch points from 100 manual steps to 1, and decreases the time to results from 4 to 10 days down to 24 to 27 hours.
By enabling whole genome sequencing (WGS) monitoring for select pathogens, Clear Dx™ offers one seamless solution within a single lab shift, helping to facilitate more timely decision-making.
Clear Dx Microbial Surveillance WGS automates the process for whole genomic sequencing of bacterial isolates utilizing short-read sequencing technology.
Clear Dx WGS SARS-CoV-2 provides fully automated whole genome sequencing of RNA extracts and assembled FASTA files utilizing long-read sequencing technology.
The Clear Dx FlexPro: Wastewater (SARS-CoV-2) provides fully automated whole genome sequencing of RNA extracts of SARS-CoV-2 from wastewater utilizing short-read sequencing technology.
Clear Dx™ allows you to generate the same outcome repeatedly—which reduces workflow errors, increases the consistency of results, boosts your overall productivity, and ultimately improves your organization’s genomic surveillance.
Through pathogen sequencing automation, Clear Dx™ helps you connect insights with unparalleled speed and precision.
Clear Dx helps you generate accurate test results that you can act on with confidence.
With our comprehensive Clear Dx™ workflow, you can manage and interpret your data—and act on it accordingly—without the need for bioinformatics specialists. Featured in the platform are data integration and connectivity solutions that help to streamline genomic surveillance.
The Clear Dx™ software offering for genomic metadata analysis places high priority on protecting the integrity and availability of customer data.
Open API integration as well as sequencing files and quality metrics for each sample are available for download after analysis.
Perform simplified sample registration and result analysis without the need for manual, error-prone interaction.
Clear Dx’s comprehensive and fully automated sequencing platform significantly reduces the level of effort typically required for infectious disease surveillance.
Our whole genome sequencing (WGS) workflow consists of only one human touchpoint vs. a hundred.
Increase lab tech productivity through automated sequencing, as technologists can perform other tasks after loading samples onto the Clear Dx™ instrument.
Learn how the Clear Dx™ platform performs versus existing methods.