Nothing
## ----setup, include = FALSE---------------------------------------------------
knitr::opts_chunk$set(
collapse = TRUE,
comment = "#>"
)
## ----eval = FALSE-------------------------------------------------------------
# remotes::install_github("wangziyue57/TaxNorm")
## ----eval = FALSE-------------------------------------------------------------
# library(TaxaNorm)
# # library(phyloseq)
# # library(microbiome)
# # library(ggplot2)
# # library(vegan)
# # library(MASS)
## ----eval = FALSE-------------------------------------------------------------
# data("TaxaNorm_Example_Input", package = "TaxaNorm")
#
# # run normalization
# TaxaNorm_Example_Output <- TaxaNorm_Normalization(data= TaxaNorm_Example_Input,
# depth = NULL,
# group = sample_data(TaxaNorm_Example_Input)$body_site,
# meta.data = NULL,
# filter.cell.num = 10,
# filter.taxa.count = 0,
# random = FALSE,
# ncores = 1)
#
# # run diagnosis test
# Diagnose_Data <- TaxaNorm_Run_Diagnose(Normalized_Results = TaxaNorm_Example_Output, prev = TRUE, equiv = TRUE, group = sample_data(TaxaNorm_Example_Input)$body_site)
#
#
## ----eval = FALSE-------------------------------------------------------------
# data("TaxaNorm_Example_Input", package = "TaxaNorm")
#
## ----eval = FALSE-------------------------------------------------------------
# qc_data <- TaxaNorm_QC_Input(TaxaNorm_Example_Input)
## ----eval = FALSE-------------------------------------------------------------
# filter.sample.num =1
# filter.taxa.count = 10
# taxaIn <- rowSums(abundances(TaxaNorm_Example_Input) > filter.taxa.count) > filter.sample.num
# TaxaNorm_Example_Input <- prune_taxa(taxaIn, TaxaNorm_Example_Input)
## ----eval = FALSE-------------------------------------------------------------
# taxaIn <- rowSums(abundances(TaxaNorm_Example_Input)) > 10
# TaxaNorm_Example_Input <- prune_taxa(taxaIn, TaxaNorm_Example_Input)
## ----eval = FALSE-------------------------------------------------------------
# qc_data <- TaxNorm_QC_Input(TaxaNorm_Example_Input)
## ----eval = FALSE-------------------------------------------------------------
# #Pick group from phyloseq object
# group <- sample_data(TaxaNorm_Example_Input)$body_site
# #Run Normalization function
# Normalized_Data <- TaxaNorm_Normalization(data = TaxaNorm_Example_Input,
# depth = NULL,
# group = group,
# filter.taxa.count = 0,
# random = TRUE,
# ncores = 1)
#
## ----eval = FALSE-------------------------------------------------------------
#
# data("TaxaNorm_Example_Output", package = "TaxaNorm")
#
#
# TaxaNorm_Model_QC(TaxaNormResults = TaxaNorm_Example_Output)
## ----eval = FALSE-------------------------------------------------------------
#
# TaxaNorm_NMDS(TaxaNormResults = TaxaNorm_Example_Output, group_column = "body_site")
#
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