nanoplexer is a standard tool to demultiplex Nanopore long read sequencing data. It extracts front and rear 150bp sequences to align aginst barcode sequences and identify the best hit. To install nanoplexer,
git clone https://github.com/hanyue36/nanoplexer.git
cd nanoplexer && make
The only library dependency is zlib
conda install -c bioconda nanoplexer
- demultiplex data according to barcode file
./nanoplexer -b barcode.fa -p output_path -t 8 input.fastq
- demultiplex data and output alignment information
./nanoplexer -b barcode.fa -p output_path -l log input.fastq
- demultiplex data from stdin stream
cat sequence_id*.fastq | ./nanoplexer -b barcode.fa -p output_path -
- demultiplex data according to dual barcode file
./nanoplexer -b barcode.fa -d dual_barcode_pair.txt -p output_path input.fastq
- Format for dual barcode pair file
Tab-delimited for each line: output file name, 5' barcode name, 3' barcode name
Please use the Issues page if you have questions. You may also directly contact Yue Han at hanyue89tj@gmail.com.