This is a fork of the original repo. I might be taking this tool into a different direction to what was originally intended
A cellular barcode demultiplexing tool of FASTQ files
git clone https://github.com/serine/sabre
cd src
makesabre -f MultiplexRNASeq_S1_R1_001.fastq.gz \
-r MultiplexRNASeq_S1_R2_001.fastq.gz \
-b barcodes.txt \
-c \
-u \
-m 2 \
-l 10 \
-a 1 \
-s sabre.txt \
-t 12This tool is under development and this is very much an alpha version In it's current form the tool is highly customised a particular multiplexing protocol
In order to demultiplex the use needs to provide barcodes.txt file, which is three column tab delimited file
sample_name group barcode
currently group is semi-redundant column, it there for a feature that in the development. for most use cases group can equals to barcode
e.g
cntr_rep1 TAAGGCGA TAAGGCGA
cntr_rep2 CGTACTAG CGTACTAG
treat_rep1 AGGCAGAA AGGCAGAA
treat_rep2 TCCTGAGC TCCTGAGC