Copy the pipeline file sn-rna-seq-parsebio.smk
, the scripts
folder and the barcodes
folder into the base directory of the sequencing run.
The script also expects
1. a folder starting with six digits (the date). Inside this folder should be the Sample Sheet (SampleSheet.csv
) with relevant names and barcodes. For more information on what the Sample Sheet should look like, see XXX.
2. If basecalled already, add all .fastq.gz
files into a folder called 01_basecalled
.
Stuff about version control etc...
kit | chem | nwells | bc1 | bc2 | bc3 | ktype |
---|---|---|---|---|---|---|
custom | NA | 1 | NA | NA | NA | special |
WT_mini | v1 | 12 | n24_v4 | v1 | v1 | normal |
WT_mini | v2 | 12 | n24_v4 | v1 | v1 | normal |
WT | v1 | 48 | v2 | v1 | v1 | normal |
WT | v2 | 48 | n96_v4 | v1 | v1 | normal |
WT_mega | v1 | 96 | n192_v4 | v1 | v1 | normal |
WT_mega | v2 | 96 | n192_v4 | v1 | v1 | normal |