Single-Cell RNA-seq Analysis
Cell Population & State Discovery
We build complete single-cell workflows that reveal cell populations, disease-specific cell states, treatment response programs, and cell-type-specific gene expression changes. From raw count matrices to annotated atlases and trajectory models, every step is documented in reproducible notebooks and presented with publication-ready figures.
Key Features
QC, Normalisation & Batch Correction
Cell and gene filtering, doublet detection, normalisation, and batch correction ensure a clean, comparable foundation across samples and conditions.
Dimensionality Reduction & Clustering
UMAP/t-SNE embeddings, graph-based clustering, and marker discovery partition the transcriptional landscape into interpretable cell populations.
Cell-Type Annotation & Reference Mapping
Canonical marker panels and reference-atlas mapping assign confident identities to each cluster, cross-validated against published cell-type signatures.
Trajectory, Ligand–Receptor & Pathway Activity
Pseudotime and trajectory inference, differential abundance, cell-type-specific DE, ligand–receptor signalling, and pathway activity scoring connect cell states to biology.