Genomics & transcriptomics

Single-Cell RNA-seq Analysis

We analyse single-cell RNA-seq datasets from count matrices to annotated cell populations and between-condition comparisons, with every filtering and clustering choice documented and figures ready for a manuscript.

Graph-based clusters of single cells shown in a UMAP embedding. Distances between clusters in UMAP space are not quantitative.

Who it is for

  • Labs with 10x Genomics or similar droplet data
  • Projects comparing conditions or time points across samples

What you send us

  • Cell Ranger outputFiltered or raw matrix, features and barcodes.
  • h5ad or Seurat objectsExisting analyses to extend or review.
  • Sample metadataDonor, condition, batch and chemistry.

What you receive

  • Annotated object (h5ad or RDS)
  • Cluster markers and annotation evidence
  • UMAP, dot-plot and composition figures
  • Pseudobulk differential-expression tables
  • Methods and notebooks

Methodology

How the work runs

Each step is agreed with you and documented. Typical tools: Scanpy · Seurat · scrublet · Harmony · scVI · CellTypist · DESeq2 (pseudobulk)

  1. ScopingSamples, conditions, expected cell types and the comparisons that matter.
  2. QC and filteringCell and gene filtering, doublet and ambient-RNA handling, with thresholds documented per sample.
  3. Integration and clusteringNormalisation, integration across samples and graph-based clustering at a justified resolution.
  4. AnnotationMarker- and reference-based cell-type annotation, reviewed with you before it is final.
  5. Comparison and reportCell-type composition and pseudobulk differential expression between conditions.

Quality controls

Checks applied to every project

  • Per-sample QC distributions and thresholds reported
  • Doublet rate estimated against the expected rate for the loading
  • Integration checked for over-correction of biological differences
  • Cluster stability across resolutions and random seeds

Scope and limits

What the work can and cannot show

  • Between-condition comparisons need biological replicates (donors or animals), not only many cells.
  • Research use only: results are not a clinical or diagnostic report.

Free quote

Start a Single-Cell project.

Describe your data and questions. We reply with questions or a written quote.

Sent securely to [email protected]. Your details are used only to process this request.

FAQ

Frequently asked questions

Not answered here? Send us your question and we will reply by e-mail.

It depends on the data type, the number of samples and the depth of interpretation you need. Every project receives a written quote with scope, deliverables, price and delivery date after a short exchange about your data and questions. The quote is free and carries no obligation.

Data are used only for your project, transferred through a channel you approve and deleted at the end of the engagement on request. We will sign your institution’s confidentiality agreement before any data are shared.

Yes. You receive a methods section with software versions and parameters, and every figure can be regenerated from the delivered code. Authorship or acknowledgement follows your field’s norms and is agreed at the start.