Single Cell Visualization - STAR-Fusion/STAR-Fusion GitHub Wiki

Results from running STAR-Fusion on single cell data can be viewed with cirrocumulus.

Cirrocumulus can simultaneously view fusions and single-cell data processed with popular tools such as Seurat, Scanpy, or Cumulus.

Installation

pip install cirrocumulus

Running

Launch cirrocumulus from the command line using the command cirro launch <dataset>... where dataset can be an h5ad, loom, a Seurat object, or fusion_predictions_deconvolved tsv file. For example:

cirro launch /data/test_samples_fusion_predictions_samples_deconvolved.tsv,/data/test_samples.h5ad.

File Formats

  • fusion_predictions_deconvolved.tsv generated by STAR-Fusion
  • h5ad
  • loom
  • Seurat object

Screenshot

Screenshot

This figure shows the fusion SS18--SSX1 and scRNA-seq data for the gene SSX1 generated using a TSNE embedding. Cells with the fusion are highlighted.

scRNA-seq Analysis Quick Start

  1. Install Pegasus via pip: pip3 install pegasuspy
  2. Run pegasus cluster with your count matrix as input to normalize, filter, cluster, and generate embeddings: pegasus cluster --louvain --tsne test_dge.txt.gz test.h5ad.

More in-depth scRNA-seq tutorials are available using Seurat, Scanpy, and Pegasus

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