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Copy pathCalculating_diversity.R
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Calculating_diversity.R
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for (fiber_subset in c("Arabinoxylan", "LCInulin", "Mix")) {
load(paste("/Users/SLancaster/Desktop/Projects/Fiber/Multiomics/RData/taxa/Normalized_Log_",fiber_subset,"species_metaphlan_df.RData",sep=""))
library(vegan)
normalized_metaphlan_df <- data.frame(t(normalized_metaphlan_df))
normalized_metaphlan_df <- 0.001 + normalized_metaphlan_df
shannon_diversity <- c()
simpson_diversity <- c()
#Generating the diversity calculations for each time point
for (i in 1:ncol(normalized_metaphlan_df)) {
sample_diversity <- diversity(as.numeric(as.matrix(normalized_metaphlan_df[,i])))
print(sample_diversity)
shannon_diversity <- c(shannon_diversity, sample_diversity)
sample_diversity <- diversity(as.numeric(as.matrix(normalized_metaphlan_df[,i])), index = "simpson")
simpson_diversity <- c(simpson_diversity, sample_diversity)
}
if (fiber_subset == "Mix") {
sorted_order = c("Baseline", "10", "20", "30", "WashoutD3", "WashoutD10")
} else {
sorted_order = c("Baseline", "10", "20", "30", "WashoutD3", "WashoutD10","WashoutFinal")
}
#Testing the differences in diversity statistically
dim(metaphlan_metadata)
for_manova <- cbind(shannon_diversity, simpson_diversity, metaphlan_metadata)
save(for_manova,file = paste("/Users/SLancaster/Desktop/Projects/Fiber/Multiomics/RData/taxa/species_diversity_",fiber_subset,".RData",sep=""))
manova_dose <- as.factor(for_manova[which(for_manova$Dose %in% c("Baseline", "30")),]$Dose)
manova_diversity <- as.numeric(as.matrix(for_manova[which(for_manova$Dose %in% c("Baseline", "30")),]$shannon_diversity))
#manova_dose <- as.factor(for_manova$Dose)
#manova_diversity <- as.numeric(as.matrix(for_manova$shannon_diversity))
fit <- anosim(manova_diversity, manova_dose)
plot(manova_dose, manova_diversity)
}