Description Usage Arguments Value
View source: R/decontaminate.R
Remove contaminant reads from a fastq file
1 2 | decontaminate(fastq_file, decontam_file, index_dir, out_file,
threads = 1)
|
fastq_file |
Path to the fastq file to be filtered. Can be in '.gz' compressed format |
decontam_file |
Path to decontam output, in .xlsx format |
index_dir |
Directory in which to store downloaded genomes and bowtie2 indices |
out_file |
Path to which the filtered fastq should be written |
threads |
How many threads should bowtie2 use when aligning (default 1) |
Returns a [tibble][tibble::tibble-package] of reads that have been removed and their taxonomic assignments
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