End to End Sequencing Solutions

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.

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Illumina Short-Read

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.

High-Throughput Performance

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

Clinical-Grade
Accuracy

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

Fast Turnaround
Time

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

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

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.

Structural Variant Detection

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

Native Methylation Profiling

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

Phasing and Haplotyping

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

Real-Time Sequencing

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

Full support for all sample types: blood, saliva, tissue, FFPE, and more
Data delivered as FastQ, VCF, or fully interpreted clinical reports — in your preferred format
Customisable sequencing outputs with clinical-grade accuracy
30X WGS as gold standard with flexible lower coverage tiers available
CAP-accredited and ISO 15189 certified
All data stored on sovereign Microsoft Azure cloud with full air-gap isolation
Encrypted end-to-end data pipeline
Largest omics lab outside the USA
High-Throughput Performance

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

High-Throughput Performance

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

High-Throughput Performance

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

High-Throughput Performance

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

Capabilities

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

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

Customisable sequencing outputs with clinical-grade accuracy

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

CAP-accredited and ISO 15189 certified

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

Encrypted end-to-end data pipeline

Largest omics lab outside the USA

From Sample to Impact: The Population Genomics Journey

We uniquely orchestrate a seamless, integrated and customizable turnkey solution for population genomics

Outreach and Sample Collection

Sample
Transportation

Preparation &
Sequencing

Data Storage
and access

Data Processing
& BIX

Modular
Applications

White Papers

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White Papers & Though Leadership

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Actionable genetic insights for better health and patient care with extra care

Through engagement with the Genomics England Research Network

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Actionable genetic insights for better health and patient care with extra care (1)

Through engagement with the Genomics England Research Network

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Actionable genetic insights for better health and patient care with extra care (2)

Through engagement with the Genomics England Research Network

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