Align reads from a fastq file against a bowtie2 index
1 | align_reads(fastq_file, index_path, species, threads = 1)
|
fastq_file |
Path of the fastq file to be aligned |
index_path |
Path of the bowtie2 index |
species |
Name of the contaminant species |
threads |
How many threads should bowtie2 use (default 1) |
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