Omics Analysis
Analysis you can defend in a review.
Practice Overview
We take raw sequencing, mass-spec or array data through QC, processing, statistics and interpretation. Every result comes with the methods, the code and the environment needed to reproduce it.
Core Capabilities
Genomics
Germline and somatic variant calling, structural variants, CNVs, annotation and prioritisation. Short-read and long-read (ONT, PacBio).
Transcriptomics
Bulk RNA-seq differential expression, splicing and fusion detection. Single-cell and spatial: clustering, annotation, trajectories, cell–cell communication.
Epigenomics
ATAC-seq, ChIP-seq and CUT&Tag peak calling, differential accessibility, motif analysis. Bisulfite and nanopore methylation.
Proteomics & metabolomics
Label-free and TMT quantification, imputation, differential abundance, pathway enrichment.
Microbiome & metagenomics
Taxonomic profiling, assembly and binning, functional annotation, AMR gene detection, diversity statistics.
Multi-omics integration
Factor models, network integration and joint embeddings that connect layers instead of stapling results together.
Key Deliverables
- ✓Analysis-ready matrices, variant tables and annotated objects
- ✓A written report with methods you can paste into a manuscript
- ✓Publication-quality static figures and interactive views
- ✓Reproducible notebooks with pinned environments
