/scISOseq_processing

Scripts to process

Primary LanguagePython

scISOseq_processing

Scripts to process scISOseq data and run scRNAseq analysis.

scISOr-Seq Workflow for final annotation

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Folders

Custom_Scripts: contains scripts written for the processing of scISOr-Seq data and assigning ensembl ids after tama merge.

scRNAseq_cellranger_and_analysis: contains scripts to run cell ranger and complete Seurat analysis

IsoSeq_processing: contains scripts written to process Iso-Seq and scISOr-Seq data using the Pacbio SMRT PacBio SMRTAnalysis software, minimap2, cDNA cupcake, and sqanti3

Tama: scripts used to run tama merge and convert to gtf

Important Notes

scISOr_Seq_processing.py requires that the input file be in fastq format. Additionally, if using the single cell flag, it requires a list of the cell barcodes. These barcodes can be taken from the barcovdes.tsv.gz file in the filtered feature bc matrix folder of a seurat output by using the below command.

zcat barcodes.tsv.gz | cut -f 1 -d "-" > barcodes_nodash.tsv