End-to-End scRNA-seq Workflow
Process single-cell RNA-seq data from raw count matrices to biologically interpretable clusters and markers.
A practical course taught live in ScarfWeb, our browser-based GUI workbench for single-cell analysis. Your team goes from raw count matrices to confident biological insight in under 3 hours.
Instructors demo the full single-cell workflow in ScarfWeb, Nygen's no-code GUI workbench for single-cell analysis. Participants follow along in the browser with no local compute and no software to install. Existing results from Seurat, Scanpy, or Bioconductor pipelines can be imported whenever they help.
Core capabilities your team builds during the session.
Process single-cell RNA-seq data from raw count matrices to biologically interpretable clusters and markers.
Navigate upload, quality control, integration, exploration, and export confidently in the ScarfWeb GUI.
Interpret quality control metrics, tune filters, and correct batch effects across experiments.
Annotate cell types with marker evidence to uncover meaningful biological insights.
Define cell selections, set up contrasts, and interpret differential gene expression results.
A structured 2.5-hour journey from raw data to publishable results. CITE-seq and HTO upload can be covered during the data steps where audience interest allows.
Course goals, what single-cell analysis can answer, and how the session is structured. (5 min)
From sequencing to count matrices: what the data is and how it reaches ScarfWeb. (15 min)
Upload count matrices, attach metadata, and set up your project in the workbench. (15 min)
Configure the analysis, choose parameters, and apply best practices for reproducible workflows. (25 min)
Open session with the instructors to discuss your own data and analysis questions. (10 min)
Explore embeddings, inspect clusters, and read what the structure is telling you. (10 min)
Assess data quality and correct batch effects before drawing conclusions. (10 min)
Assign cell types from marker evidence and review annotation confidence. (10 min)
Create cell selections and run differential gene expression between groups of interest. (15 min)
Publish and share results, export outputs, and recap next steps. (15 min)
Each part of the live session maps to a step you run yourself in the workbench.
Bring in preprocessed count matrices in common formats and attach sample and cell-level annotations.
Filter cells by quality metrics and select highly variable genes with adjustable thresholds.
Harmonize datasets across experiments, then run dimensionality reduction for joint analysis.
Navigate cluster embeddings, inspect groups, and define cell selections for downstream comparisons.
Compare cell groups, identify marker genes, and interpret statistical outputs in context.
Publish findings, generate shareable links, and export outputs for further analysis.
Built for teams that need practical single-cell analysis fluency.
Build clear analysis instincts early and understand why each workflow step matters.
Interpret outputs with confidence and connect single-cell results to biological decisions.
Standardize best practices across projects and support users on reproducible workflows.
Learn directly from domain experts in single-cell biology and computational genomics.
Co-founder and Head of Partnerships, Nygen
PhD, Associate Professor in Molecular Hematology, Lund University.
Co-founder and CEO, Nygen
PhD, Computational Genomics.
We bring the course to you. Free for core facilities, research groups, and academic institutions.