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World-Class Sequencing, Ready to Scale

From sample collection to secure data delivery, Biogenix provides end-to-end sequencing services for clinical laboratories, research institutions, pharmaceutical companies, and national health programs. Our capabilities cover logistics, sample processing, high-throughput sequencing, and automated data analysis, ensuring speed, accuracy, and reliability at every step.

We offer short-read and long-read NGS-based sequencing to support a broad range of applications, including rare disease diagnosis, oncology testing, drug discovery, biomarker research, population-scale genomic programs, and translational research. All sequencing is performed in CAP-accredited, ISO 15189 certified facilities, with data delivered securely and in your preferred format.

  • Illumina Short-Read

    NovaSeq X and NovaSeq 6000 platforms, clinical-grade short-read sequencing, rapid turnaround.

    Running on NovaSeq X and NovaSeq 6000 platforms, we primarily deliver whole genome sequencing at clinical grade and population scale, with the flexibility to support targeted sequencing applications where required.

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    High-Throughput Performance

    Process thousands of samples in parallel at clinical and research scale, without compromising quality or turnaround.

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    Clinical-Grade
    Accuracy

    Validated workflows and deep coverage ensure high sensitivity and specificity across diagnostics, screening, and genomic reporting.

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    Fast Turnaround
    Time

    Optimised protocols and automation deliver results with minimal delay, critical for time-sensitive applications such as newborn screening and oncology.

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    Scalable for Any Use Case

    From whole genome sequencing to targeted applications, our service adapts to your project size, application, and scientific requirements.

  • Oxford Nanopore Long-read

    Long-read sequencing with native methylation profiling, structural variant detection, and real-time capability.

    Our Oxford Nanopore long-read sequencing service is designed for researchers and discovery programs requiring resolution that short-read sequencing cannot provide. We support structural variant detection, repeat expansion analysis, complex region phasing, and native methylation profiling, all from a single sequencing run without additional preparation steps.

    Long-read sequencing is particularly suited to rare disease research, epigenomic studies, and projects requiring deep biological characterisation at population scale. All data is processed and delivered securely from our state-of-the-art sequencing facility.

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    Structural Variant Detection

    Identify large-scale genomic rearrangements and complex variants that short-read sequencing cannot resolve.

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    Native Methylation Profiling

    Capture epigenomic data directly from sequencing — no additional library preparation required.

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    Phasing and Haplotyping

    Resolve complex genomic regions and determine variant phasing with greater accuracy than short-read approaches.

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    Real-Time Sequencing

    Adaptive sequencing and real-time data analysis for time-sensitive research and clinical applications.

Capabilities

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Full support for all sample types: blood, saliva, tissue, FFPE, and more

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Data delivered as FastQ, VCF, or fully interpreted clinical reports — in your preferred format

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Customisable sequencing outputs with clinical-grade accuracy

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30X WGS as gold standard with flexible lower coverage tiers available

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CAP-accredited and ISO 15189 certified

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All data stored on sovereign Microsoft Azure cloud with full air-gap isolation

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Encrypted end-to-end data pipeline

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Largest omics lab outside the USA

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