CALYPSO™

Your NGS Sample Preparation Automation

A revolutionary sequencing platform that offers a fully automated solution for nucleic acid extraction and library preparation, streamlining your old NGS workflow and eliminating the time-consuming and error-prone manual steps.

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What is CALYPSO™ ?

Calypso product shot taken from the side

CALYPSO™, our innovative system efficiently processes a wide variety of raw samples, including both DNA and RNA, generating high-quality, sequence-ready libraries within a remarkable timeframe of under 2 hours. Pre-loaded onboard reagents and our proprietary system work in tandem to minimize sample loss and ensure consistent processing across experiments. By empowering researchers with a robust platform for streamlined NGS workflows, CALYPSO™ accelerates discovery and maximizes research output.

CALYPSO™ - Revolutionizing NGS Sample Prep

Faster Sequencing

CALYPSO™ streamlines your genomic processing. It extracts and purifies DNA and RNA from raw samples, and prepares the sample to be sequence-ready—all within 2 hours and without any human involvement, elevating your genomic processing to the next level.

Versatile & Flexible

From analyzing intricate wastewater microbial communities to investigating pathogens in pure cultures, or from exploring the genetic makeup of plant tissues to venturing into new areas of NGS research, CALYPSO™ adapts to your specific needs and seamlessly integrates into your existing workflow.

Data analysis quantitative result bar chart with a magnifying glass

With CALYPSO™, you can bid farewell to the tedious manual labour and welcome a new era of hands-free, error-free library preparation. By employing innovative technology, the cutting-edge solution automates sequencing library preparation with precision and efficiency.

Intuitive & Reliable

CALYPSO™ is engineered to be compatible with a wide range of sequencing platforms, including Oxford Nanopore, Illumina, and PacBio systems. Whether you're performing long-read sequencing, short-read sequencing, or nanopore sequencing, Calypso™ has you covered.

Cross-Platform Compatibility

What Can CALYPSO™ Help?

1. Sample Input

2. Nucleic Acid Extraction

Amplification Process of DNA Sequencing Preparation

3. Amplification (Optional)

4. Fragmentation

Fragments Size Selection in DNA Sequencing Preparation

5. Size Selection

Calypso DNA Sequecing Preparation Clean-Up Process

6. Clean-up

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7. Library Quality Control

Ligation Process in DNA Sequencing preparation

8. Adapter Ligation

CALYPSO™ begins by effortlessly extracting high-quality nucleic acids, either DNA or RNA from your sample of choice, ensuring purity and integrity throughout the process. Enzymatic fragmentation swiftly transforms nucleic acids into smaller fragments suitable for sequencing, setting the stage for precise downstream analysis. End repair and adenylation processes further refine DNA fragments, priming them for efficient adapter binding and subsequent sequencing. With customizable size selection, clean-up, and quantification protocols, CALYPSO™ delivers libraries of unparalleled quality and concentration, tailored to your experimental needs. Complete your library preparation journey with confidence as CALYPSO™ facilitates adapter ligation, seamlessly preparing your libraries for sequencing on leading platforms such as Oxford Nanopore, Illumina, or PacBio.