Sequencing and multiomics platforms

    Instead of forcing trade-offs between scale, flexibility, data quality, and usability, we build systems with a clear purpose, so researchers can choose the platform that fits their work.

    Our platforms include VITARI™, AVITI24™, AVITI™, and AVITI LT™ spanning mid-throughput, multiomics, and high-throughput sequencing applications.

    Designed with intent, built for your discovery

    At Element, we innovate to meet researchers where they are today and where their science is headed tomorrow. We build platforms around real lab needs: reliable, high-quality performance, practical workflows, and room to grow so you can focus on discovery. And we keep evolving what we deliver, so your platform stays aligned with new applications, new questions, and new possibilities.

    VITARI

    Designed for high-throughput sequencing without compromises.

    VITARI is a high-throughput sequencing platform designed to deliver scale without sacrificing flexibility, usability, or data quality. It delivers up to 10 billion reads or 3 TB of data per dual-sided run, enabling a $100 genome with >90% Q30 quality.

    With two independent flow cells, each with six lanes, VITARI supports flexible, right-sized run configurations, allowing researchers to scale output while minimizing wasted capacity. VITARI will be available in H2 of 2026.

    AVITI24

    Designed for integrated single-cell, spatial multiomics and high-quality sequencing.

    AVITI24 is an integrated sequencing and single-cell multiomics platform designed to enable simultaneous analysis of DNA, RNA, proteins, phosphorylated proteins, and cell morphology from a single sample without library prep, supporting deeper biological insight without fragmented workflows or multiple instruments.

    It also delivers high-quality sequencing with up to 50% greater sequencing output than the AVITI, with the same quality, flexibility, and affordability.

    AVITI

    Designed for flexible, everyday mid-throughput sequencing

    AVITI is a cost-effective, high-quality, mid-throughput sequencing platform designed to support a wide range of applications with flexible run configurations, allowing researchers to right-size each run without batching.

    AVITI delivers cost-effective sequencing across diverse output needs, from 100 million to 2 billion reads experiments, while maintaining industry-leading performance and data quality. The AVITI can be upgraded to the multiomic capabilities of the AVITI24.

    AVITI LT

    Designed for focused sequencing with lower instrument cost

    AVITI LT is a low-throughput version of AVITI that brings high-quality ABC™ sequencing to more users with a lower instrument cost. It is the ideal choice for smaller-scale projects or research labs with a small range of applications or limited capital equipment budget.

    AVITI LT enables researchers to access Element sequencing performance in a lower-throughput configuration, while preserving the ability to upgrade to the AVITI or AVITI24 as their research evolves.

    Platform Overview

    Features AVITI LT AVITI AVITI24 VITARI
    Core NGS Output
    (reads/FC)a
    500 million 1 billion 1.5 billion 5 billion
    Dual Independent Flow Cells yes yes yes yes
    Individually Addressable Lanes yes yes yes yes
    Cloudbreak Freestyle™ yes yes yes yes
    Cloudbreak UltraQ™
    (>70% Q50+)
      yes yes  
    Trinity™   yes yes yes
    Core NGS Quality
    >90% >Q30
    yes yes yes yes
    Direct in sample multiomics     yes Future upgrade
    Upgrade Options Upgrade Available to AVITI or AVITI24 Upgrade Available to AVITI24 N/A  N/A

    a Performance metrics are based on sequencing Element 2x150 libraries. Actual results might differ based on factors such as library type and preparation.

     

    Powered by Avidite Base Chemistry™

    Our AVITI line of systems are built on Avidite Base Chemistry (ABC™), enabling unparalleled accuracy and efficiency in nucleotide detection. By utilizing a unique combination of enzymatic and chemical processes, ABC enhances the specificity and sensitivity of base calling, resulting in high-fidelity sequencing data with minimal errors. This innovative technology enables researchers to confidently explore the complexities of the genome, from identifying rare variants to unraveling intricate genetic pathways.

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