# Import Data library(tidyverse) theme_set(theme_bw()) library(phyloseq) devtools::load_all() load('~/Projects/Mine/aftersl1p/benchmark/data.RData') seqs = rownames(asv_tab) all(seqs == rownames(tax_tab)) rownames(asv_tab) = rownames(tax_tab) = NULL head(map_tab) map_tab = (map_tab %>% mutate(ContVar = c(13.6, 8.3, 2.8, 15.5, 10, 6.6, 13.0, 11.5))) rownames(map_tab) = map_tab$SampleID setdiff(colnames(asv_tab), rownames(map_tab)) asv_tab = as.matrix(asv_tab) tax_tab = as.matrix(tax_tab) dat = phyloseq(otu_table(asv_tab, taxa_are_rows = TRUE), tax_table(tax_tab), sample_data(map_tab)) # Clean Data dat dat = prop_tax_down(dat, indic = FALSE) dat_rel = transform_sample_counts(dat, function(x) x/sum(x)) keep = taxa_sums(dat)/nsamples(dat) >= 100 dat_filt = prune_taxa(keep, dat) dat_rel_filt = prune_taxa(keep, dat_rel) col_vect = c("#E41A1C","#377EB8","#4DAF4A","#984EA3","#FF7F00", 'dodgerblue2', 'goldenrod3', 'pink')
plot_read_depth(dat_filt)
plot_read_depth(dat_filt, xvar = 'Source')
plot_read_depth(dat_filt, cvar = 'ContVar')
plot_read_depth(dat_filt, cvar = 'Source', xvar = 'SampleID') plot_read_depth(dat_filt, cvar = 'Source', xvar = 'Source')
plot_read_depth(dat_filt, cvar = 'SampleID')
plot_read_depth(dat_filt, clrs = col_vect[1])
plot_read_depth(dat_filt, clrs = col_vect)
Raises an error. See testthat
tests
col_hl = col_vect[1:2] names(col_hl) = c('low','high') col_hl plot_read_depth(dat_filt, cvar = 'ContVar', clrs = col_hl)
plot_read_depth(dat_filt, cvar = 'SampleID', clrs = col_vect)
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