| transform_pq | R Documentation |
Single entry-point for all count-table transformations available in
MiscMetabar. Ecological methods ("tss", "hellinger", "clr",
"rclr", "log1p", "z", "pa", "rank") are delegated to
vegan::decostand(). Library-size normalisation methods ("rarefy",
"srs", "gmpr", "css", "tmm", "vst") and the McKnight
log-log residual method ("mcknight_residuals") are delegated to
their dedicated *_pq() functions. All ... arguments are forwarded
to the underlying function.
transform_pq(
physeq,
method = c("tss", "hellinger", "clr", "rclr", "log1p", "z", "pa", "rank",
"normalize_prop", "rarefy", "srs", "gmpr", "css", "tmm", "vst", "mcknight_residuals"),
pseudocount = 1,
...
)
physeq |
(required) a |
method |
(character, default
|
pseudocount |
(numeric, default |
... |
Additional arguments forwarded to the underlying function
( |
A new phyloseq-class object with a
transformed otu_table (and augmented sample_data for
"mcknight_residuals").
Adrien Taudière
normalize_prop_pq(), rarefy_pq(), srs_pq(), gmpr_pq(),
css_pq(), tmm_pq(), vst_pq(), mcknight_residuals_pq(),
as_binary_otu_table(), vegan::decostand()
data_f_tss <- transform_pq(data_fungi_mini, method = "tss")
sample_sums(data_f_tss)
data_f_hell <- transform_pq(data_fungi_mini, method = "hellinger")
data_f_clr <- transform_pq(data_fungi_mini, method = "clr")
data_f_rclr <- transform_pq(data_fungi_mini, method = "rclr")
data_f_log1p <- transform_pq(data_fungi_mini, method = "log1p")
data_f_z <- transform_pq(data_fungi_mini, method = "z")
data_f_pa <- transform_pq(data_fungi_mini, method = "pa")
data_f_rank <- transform_pq(data_fungi_mini, method = "rank")
data_f_norm_prop_log10 <- transform_pq(data_fungi_mini,
method = "normalize_prop", base_log = 10
)
data_f_norm_prop_no_log <- transform_pq(data_fungi_mini,
method = "normalize_prop", base_log = NULL
)
data_f_norm_prop_log2 <- transform_pq(data_fungi_mini,
method = "normalize_prop", base_log = 2
)
data_f_rarefy <- transform_pq(data_fungi_mini, method = "rarefy", seed = 1)
data_f_srs <- transform_pq(data_fungi_mini, method = "srs", seed = 1)
data_f_gmpr <- transform_pq(data_fungi_mini, method = "gmpr")
data_f_css <- transform_pq(data_fungi_mini, method = "css")
data_f_tmm <- transform_pq(data_fungi_mini, method = "tmm")
data_f_vst <- transform_pq(data_fungi_mini, method = "vst")
data_f_mcknight <- transform_pq(data_fungi_mini, method = "mcknight_residuals")
otu_list <- list(
hell = unclass(data_f_hell@otu_table),
clr = unclass(data_f_clr@otu_table),
rclr = unclass(data_f_rclr@otu_table),
log1p = unclass(data_f_log1p@otu_table),
z = unclass(data_f_z@otu_table),
rarefy = unclass(data_f_rarefy@otu_table)
)
pairs_cor <- sapply(
otu_list,
\(x) sapply(otu_list, \(y) cor(as.vector(x), as.vector(y)))
)
pairs_cor
plot(unclass(data_f_mcknight@otu_table), unclass(data_f_css@otu_table))
plot(unclass(data_f_rarefy@otu_table), unclass(data_f_clr@otu_table))
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