processSeq | R Documentation |
Perform dada2 analysis
processSeq(
path = ".",
truncLen = c(0, 0),
trimLeft = 0,
trimRight = 0,
minLen = 20,
maxLen = Inf,
sample_info = NULL,
train_data = "silva_nr99_v138_train_set.fa.gz",
train_species = "silva_species_assignment_v138.fa.gz",
outpath = NULL,
saveobj = FALSE,
buildtree = FALSE,
verbose = TRUE
)
path |
working dir for the input reads |
truncLen |
(Optional). Default 0 (no truncation). Truncate reads after truncLen bases. Reads shorter than this are discarded. |
trimLeft |
(Optional). The number of nucleotides to remove from the start of each read. |
trimRight |
(Optional). Default 0. The number of nucleotides to remove from the end of each read. If both truncLen and trimRight are provided, truncation will be performed after trimRight is enforced. |
minLen |
(Optional). Default 20. Remove reads with length less than minLen. minLen is enforced after trimming and truncation. |
maxLen |
Optional). Default Inf (no maximum). Remove reads with length greater than maxLen. maxLen is enforced before trimming and truncation. |
sample_info |
(Optional).sample information for the sequence |
train_data |
(Required).training database |
train_species |
(Required). species database |
outpath |
(Optional).the path for the filtered reads and th out table |
saveobj |
(Optional).Default FALSE. save the phyloseq object output. |
buildtree |
build phylogenetic tree or not(default: FALSE) |
verbose |
(Optional). Default TRUE. Print verbose text output. |
list include count table, summary table, taxonomy information and phyloseq object
Kai Guo
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