Turning complex biological data into clear, actionable insights.
Oxford Omics provides expert bioinformatics analysis, training and guidance for industry, academic and healthcare teams.
Our Services
Analysis
We provide end-to-end bioinformatics analysis for genomics, transcriptomics, and multi-omics data. This includes experimental design support, data processing, statistical analysis, and biological interpretation. Our focus is on producing robust, reproducible results that directly answer your scientific or commercial questions - not just running pipelines.
Training
We deliver practical, tailored training to help individuals and teams develop confidence in bioinformatics and computational biology. Training can be delivered as short workshops or longer programmes and is adapted to your data, tools, and research goals. The aim is to help teams understand their analyses, interpret results correctly, and work more independently over time.
Flexible support
For projects that require on-demand bioinformatics expertise, we can join your team on a flexible, part-time or project-based basis. This provides rapid access to senior-level bioinformatics support without the overhead of a full-time hire. We work alongside your scientists, contributing directly to analyses, project planning, and decision-making over weeks or months as needed.
Our Expertise
AI and Machine Learning for Biology
We design and apply artificial intelligence (AI) and machine learning methods for the analysis and interpretation of complex biological data, including genomics, transcriptomics, imaging and clinical biomarker datasets, with recent work spanning cancer prediction and generative protein design.
Single-cell RNA-Seq (including Spatial)
We provide expert analysis and interpretation of single-cell RNA-seq and spatial transcriptomics data, supporting study design, data processing, cell type annotation, differential expression, and biological interpretation across complex tissues and disease contexts.
CRISPR analysis
We work with clients to design and execute analytical workflows for CRISPR screening data, covering quality control, normalization, hit calling, and biological interpretation across genome-wide and targeted screens.
Pipelines and Data Dashboards
We design and build robust data processing pipelines and interactive dashboards to support reproducible analysis, insight discovery and effective communication of results.
Mutation Analysis
We work with research and clinical teams to design, analyze, and interpret whole-genome (WGS) and whole-exome (WES) sequencing studies, supporting confident variant prioritization and decision-making.
RNA-Seq
We support RNA-seq projects from experimental design through data processing, differential expression analysis, and biological interpretation, with a focus on robust methodology and reproducible results.
Laboratory Support
Molecular Biology
We have knowledge in a range of molecular biology techniques and optimal experimental design, particulary for omics related studies.
Cell culture
We are experts in cell culture methods, including the optimisation of induced pluripotent stem cell differentiation protocols for neurodegenerative disease models.
Library Preparation
We are experienced in performing routine and bespoke library preparations for a range of sequencing technologies, such as Illumina and Oxford Nanopore Technologies.