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Phyloseq is a
popular package for working with microbiome data. Here we show how to
use the phy_to_floral_data
helper function to convert
phyloseq data into a format accepted by FLORAL.
The following code downloads data described in this paper
and turns it into a phyloseq object. The tax_glom step here takes some
time, and can be replaced with speedyseq::tax_glom
for better performace.
#this file has duplicate rows, and has multiple rows per pool
samples <- read.csv("https://figshare.com/ndownloader/files/33076496") %>% distinct() %>%
select(-Pool, -Run, -ShotgunBatchID) %>% distinct()
samples <- samples[1:100,] # Using the first 100 samples only.
counts <- read.csv("https://figshare.com/ndownloader/files/26393788")
counts <- counts %>%
filter(SampleID %in% samples$SampleID)
taxonomy <- read.csv("https://figshare.com/ndownloader/files/26770997")
phy <- phyloseq(
sample_data(samples %>% column_to_rownames("SampleID")),
tax_table(taxonomy %>% select(ASV, Kingdom:Genus) %>% column_to_rownames("ASV") %>% as.matrix()),
otu_table(counts %>% pivot_wider(names_from = "SampleID", values_from = "Count", values_fill = 0) %>% column_to_rownames("ASV") %>% as.matrix(), taxa_are_rows = TRUE)
) %>% subset_samples(DayRelativeToNearestHCT > -30 & DayRelativeToNearestHCT < 0) %>%
tax_glom("Genus")
Next, we convert that phyloseq object into a list of results to be
used by FLORAL; we have to specify the main outcome of interest as
y
, and any metadata columns (from
sample_data(phy)
) to use as covariates. Note that the
analysis described here is just an example for using the function;
this
The resulting list has named entities for the main arguments to FLORAL:
res <- FLORAL::FLORAL(y = dat$y, x = dat$xcount, ncov = dat$ncov, family = "gaussian", ncv=NULL, progress=FALSE)
These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
Health stats visible at Monitor.