Humann2 Output Read In Read in all output files for any number of samples into a list of dataframes, containing gene abundances, pathway abundances, and pathway coverage for each sample Output information: data[[1]] = genefam (gene family abundance table) data[[2]] = pathabu (pathway abundance table) data[[3]] = pathcov (pathway coverage table) Requires pbapply and stringr libraries
1 | read_humann2(file_dir)
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1 2 | a <- "/Volumes/castoricenter/Eric.Littmann/U01/Processed_Data/Humann2/"
data <- humann2_readin(a)
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