knitr::opts_chunk$set( collapse = TRUE, comment = "#>", fig.path = "man/figures/README-", out.width = "100%" )
fqdecontamr filters fastq files to remove reads identified as potential contaminants by decontam.
You can install the development version of fqdecontamr from GitHub with:
devtools::install_github("wilkox/fqdecontamr")
fqdecontamr requires two input files:
*.xlsx
)The main function provided by fqdecontamr is called decontaminate()
. It takes
as arguments the paths to the two input files listed above ( decontam_file
and fastq_file
), a third argument index_dir
specifying a directory in which
to cache downloaded genomes and bowtie2 index files, and a fourth argument
out_file
specifying where to write the filtered fastq file. decontaminate()
returns a tibble listing the reads that were
removed and the contaminant species to which they aligned.
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