Bioinformatics consultancy · Oxford, UK

Turning complex biological data into clear, actionable insights.

Oxford Omics provides expert bioinformatics analysis, training and guidance for industry, academic and healthcare teams.

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Dr Peter Kilfeather and Dr Charmaine Lang, co-founders of Oxford Omics

Dr. Charmaine Lang & Dr. Peter Kilfeather · co-founders

Drawing on experience at the University of Oxford, the Garvan Institute of Medical Research and precision-oncology industry.

17years combined experience

40+clients

Services

What we do

Three ways of working: end-to-end analysis, practical training, or senior-level support embedded in your team.

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.

Expertise

Areas of expertise

Illustration of a brain with circuit lines and a central AI label, representing machine learning.

AI and Machine Learning for Biology

We design and apply AI and machine learning methods for complex biological data, including genomics, transcriptomics, imaging and clinical biomarker datasets, with recent work spanning cancer prediction and generative protein design.

UMAP scatter plot of coloured single-cell clusters.

Single-cell RNA-Seq (including Spatial)

Expert analysis and interpretation of single-cell RNA-seq and spatial transcriptomics data: study design, processing, cell type annotation, differential expression and biological interpretation across complex tissues and disease contexts.

DNA double helix being cut by scissors with a guide RNA strand, representing CRISPR editing.

CRISPR analysis

Analytical workflows for CRISPR screening data: quality control, normalisation, hit calling and biological interpretation across genome-wide and targeted screens.

Monitor showing analysis outputs: volcano plot, sequencing traces and result charts.

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.

Clustered heatmap with dendrogram, typical of differential-expression results.

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.

Three stylised figures wearing DNA-helix motifs, representing inherited genetic variation.

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 prioritisation and decision-making.

Laboratory support

Cell culture

We are experts in cell culture methods, including the optimisation of induced pluripotent stem cell differentiation protocols for neurodegenerative disease models.

Laboratory pipette with blue volume scale.

Molecular Biology

We have knowledge in a range of molecular biology techniques and optimal experimental design, particularly for omics related studies.

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.

Our human promise

Artificial Intelligence (AI) is opening up new possibilities for scientific discovery. At Oxford Omics, we continually review our methods to ensure we work at the cutting edge of science and technology.

We guarantee that your project will be directed by our expert human team. All analyses are strictly human-in-the-loop to provide accountability, credibility and accuracy.

When you talk to us, you talk to humans.

Schedule a free call About us

Contact

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