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## Makefile to run the example script and the test script
## -i / --input, Illumina reads file in FASTQ format
INPUT = data/example/example01.fastq
## -s / --samples, sample list where each line is the sample_name-tab-barcode(4bp)
SAMPLES = data/example/example01.txt
## -g / --genome, concatenated genbank file for all contigs for the genome
GENBANK = data/example/ES114v2.gb
## -e / --experiment, all results files will be created in the subfolder of this name
EXPERIMENT = example01
## Location of test script
TEST = test/test.py
default:
python scripts/pyinseq.py -i $(INPUT) -s $(SAMPLES) -g $(GENBANK) -e $(EXPERIMENT)
python $(TEST)