Whole-Genome Sequencing (WGS)

Sequencing solutions

OHMX.bio offers state-of-the-art sequencing solutions designed to accelerate your research and clinical breakthroughs. By leveraging cutting-edge technologies, expert bioinformatics, and extensive experience, we provide tailored sequencing strategies for a wide range of applications. From discovery research to clinical diagnostics, our services ensure precision, reliability, and unparalleled data insights. Explore how our sequencing solutions can power your next breakthrough.

Comprehensive sequencing services

Our suite of sequencing solutions is designed to meet diverse research and clinical needs. Whether you are looking for genome-wide insights or targeted analyses, OHMX.bio delivers high-quality, scalable services that provide actionable data. Our core offerings include:

Clinical Solutions

Advanced sequencing tailored to meet regulatory and diagnostic requirements. Aimed at high-throughput solutions offered under GCLP.
Clinical Solutions
RNA Sequencing

RNA Sequencing

Discover the transcriptome as a whole to investigate differences in expression between groups, or learn about alternative splicing methods.
Ribosomal Profiling

Ribosomal Profiling

A unique sequencing technique to gain insights into translational regulation by analyzing ribosome-bound mRNA.

Whole-Genome Sequencing (WGS)

Whole-Genome Sequencing (WGS)

Gain comprehensive genetic insights with our short– and long-read sequencing expertise.
Single-Cell Sequencing

Single-Cell Sequencing

Explore individual cells. Unlock detailed biological insights with single-cell sequencing.
Whole-Exome Sequencing (WES)

Whole-Exome Sequencing (WES)

Focus on coding regions for impactful mutation analysis.
Epigenetic Sequencing

Epigenetic Sequencing

Utilize Oxford Nanopore‘s bimodal readout to simultaneously analyze DNA/RNA methylation, histone modifications, and chromatin accessibility in the same sample.
Custom Sequencing Solutions

Custom Solutions

Our experts are ready to discuss your project and create tailor-made sequencing strategies, including custom enrichment kits for targeted approaches.
Each of these services is supported by our cutting-edge bioinformatics team, ensuring that your data is accurately processed, analyzed, and interpreted.

90+

Satisfied customers trusted us with their samples

190+

Solutions offered to progress research and clinical trials

22.300+ km

Of nucleotides sequenced end-to-end. That’s the earth’s diameter, twice!

Why choose OHMX.bio for sequencing?

At OHMX.bio, we go beyond data generation to deliver actionable insights. Here’s why researchers and clinicians trust us.

Scientific Expertise

As a spin-off from Ghent University, we combine academic rigor with practical application.

Advanced Technology

We leverage the latest platforms and protocols to provide accurate, reproducible results.

Customization

Our flexible approach ensures that your specific needs and objectives are met.

End-to-End Support

From sample preparation to advanced data analysis, we provide comprehensive support at every step.

Regulatory Compliance

Our services meet stringent quality standards, ensuring reliability for both research and clinical applications.

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Seamless integration across technologies

Our sequencing solutions are designed to integrate seamlessly with other -omics services, such as proteomics and transcriptomics, enabling multi-dimensional insights. By combining data from various platforms, we provide a holistic view of your biological system, enhancing the impact of your research.
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Partner with OHMX.bio

Whether you are conducting fundamental research, developing novel therapeutics, or advancing clinical diagnostics, OHMX.bio’s sequencing solutions are here to support your goals. Our commitment to innovation, quality, and client success makes us the ideal partner for all your sequencing needs.

Let’s get in touch!

Are you curious about how we can work on your -omics challenges together? Fill out the form below!
Our experts will reply within 2 working days to freely discuss your omics project.

Frequently asked questions about our sequencing solutions

OHMX.bio provides a broad portfolio of sequencing solutions, RNA sequencing, ribosomal profiling, whole-genome sequencing (WGS), whole-exome sequencing (WES), epigenetic sequencing, long-read sequencing, single-cell sequencing, and custom sequencing strategies. These services are supported by integrated bioinformatics analysis and tailored workflows to match specific research or clinical objectives. Projects can range from exploratory discovery studies to regulated diagnostic applications, ensuring flexibility and scientific rigor across use cases.
Whole-genome sequencing (WGS) analyzes the entire genome, allowing comprehensive detection of SNPs, indels, structural variants, and non-coding alterations. Whole-exome sequencing (WES) focuses specifically on protein-coding regions (exons), which represent a smaller portion of the genome but contain many disease-associated variants. WGS provides broader biological insight, while WES offers a cost-efficient approach for variant discovery in clinical and translational research settings.
OHMX.bio operates under strict quality standards, including GCLP conditions for applicable workflows. Sequencing services include end-to-end support: sample handling, quality control of samples, library preparation, sequencing, and advanced bioinformatics analysis. Regulatory compliance, reproducibility, tracability and data integrity are central to the workflow. This ensures that generated data is suitable for research, translational studies, and clinical applications requiring validated procedures.
Yes. OHMX.bio offers custom sequencing solutions tailored to specific research questions, unique sample types, or specialized enrichment strategies. Custom enrichment kits and protocol adjustments can be designed in collaboration with researchers. This flexibility ensures that each project generates biologically meaningful and actionable data aligned with defined objectives.
OHMX.bio combines academic expertise, advanced sequencing technologies, and integrated bioinformatics under one roof. As a spin-off from Ghent University and part of the Anacura Group, the company delivers high scientific standards alongside practical scalability. With extensive project experience and a strong track record, OHMX.bio supports clients from experimental design through interpretation and reporting.