Group sequences by sample index combination
Usage
do_demux(
primer_search_fq,
out_dir,
sample_tab,
error_threshold = 2.5,
min_barcode_length = 50
)Arguments
- primer_search_fq
One or multiple paths from do_primer_search (
trimmed_fqentry in the returned list).
Value
sample_tab with a reads_path column and additional rows
for samples found in the reads but not in the sample table
Details
See do_trim_demux for details on the other arguments
The read files in out_dir are named as follows: fprimer-fidx--rprimer-ridx.fastq.gz
Requires seqtool v0.4 or higher