Single-Cell RNA-Seq (scRNA-Seq) Services
Expert, end-to-end Single-Cell RNA-Seq (scRNA-Seq) Services from BioCode — send us your data and research question and we deliver the analysis, a clear report and reproducible code you can publish with confidence.
- Confidential & NDA-friendly
- Report + reproducible code
- Real research datasets
Single-cell RNA-Seq (scRNA-Seq) analysis
Single-cell RNA sequencing (scRNA-Seq) measures gene expression in individual cells, making it possible to dissect cellular heterogeneity, identify rare cell populations and map the diversity of tissues that traditional bulk RNA-Seq cannot resolve. It has transformed our understanding of development, immunology, cancer and many complex tissues.
We provide complete scRNA-Seq analysis using Seurat, Scanpy and related tools, from raw count matrices to fully annotated, biologically interpretable results.
Our Services
- Quality control, doublet detection and normalisation
- Dimensionality reduction, clustering and UMAP / t-SNE visualisation
- Cell-type annotation and marker-gene identification
- Differential expression between clusters and conditions
- Trajectory and pseudotime analysis
- Cell–cell communication and ligand–receptor analysis
- Batch-effect correction and multi-sample integration
- Gene-set and pathway-enrichment analysis
The result is a clear picture of which cell types are present and how their transcriptional programmes change across conditions, time and treatment.
Tell us about your
analysis
Share your research question and dataset and we'll get back to you with a scope, timeline and quote — usually within one to two working days.
- Attach data: PDF, DOCX, PDB, SDF, CSV, XLS, XLSX
- No-obligation quote
- Replies within 24–48 hours
