Perform single-cell RNA-seq analysis from FastQ files to cerebro file for 10XGenomics technology data.
- Alignment_countTable_GE,
- Alignment_countTable_ADT,
- Alignment_annotations_TCR_BCR,
- Droplets_QC_GE,
- Filtering_GE,
- Norm_DimRed_Eval_GE,
- Clust_Markers_Annot_GE,
- Adding_ADT,
- Adding_TCR,
- Adding_BCR,
- Cerebro.
- Integration analysis of several samples,
- Grouped analysis (no integration) of several samples,
- TCR for several samples together,
- BCR for several samples together,
- Improve cell annotation,
- ...
See complete documentation on the wiki