Single-Cell RNA-seq Nodes
scRNA-seq nodes take droplet-based sequencing data through quantification, quality control, and downstream analysis (clustering, marker genes, UMAP).
Cell Ranger count
10x Genomics’ pipeline for read alignment and per-cell gene quantification.
Inputs: reads: FASTQ, reference: Directory (transcriptome)
Outputs: matrix: Matrix, report: Report
| Parameter | Type | Default | Description |
|---|---|---|---|
expectCells | Int | — | Expected number of cells |
chemistry | String | auto | 10x chemistry version |
Cell Ranger is memory- and disk-heavy. Use Large (128 GB)+ for human data.
STARsolo
Open-source alternative to Cell Ranger built on STAR; produces a compatible count matrix.
Inputs: reads: FASTQ, reference: FASTA, annotation: GTF
Outputs: matrix: Matrix
Scanpy: QC & Filter
Loads a count matrix and computes per-cell QC metrics; filters cells/genes.
Inputs: matrix: Matrix
Outputs: adata: Matrix (h5ad), report: Report
| Parameter | Type | Default | Description |
|---|---|---|---|
minGenes | Int | 200 | Drop cells below this gene count |
maxPctMito | Float | 5.0 | Drop cells above this % mito reads |
Scanpy: Cluster & Embed
Normalization, PCA, neighbors, Leiden clustering, and UMAP embedding.
Inputs: adata: Matrix
Outputs: adata: Matrix, umap: Report
| Parameter | Type | Default | Description |
|---|---|---|---|
nPCs | Int | 50 | Principal components |
resolution | Float | 1.0 | Leiden clustering resolution |
A typical scRNA-seq pipeline
[FASTQ Input] → [Cell Ranger count] → [Scanpy QC & Filter] → [Scanpy Cluster & Embed] → [Report Output]See also
- Data Types — the
Matrixtype - Assembly nodes