Alpha and beta diversity analysis for microbiome data. Calculate within-sample richness, evenness, and between-sample dissimilarity with phyloseq and vegan. Use when comparing community composition across samples or testing for group differences in microbiome structure.
Reference examples tested with: R stats (base), ggplot2 3.5+, phyloseq 1.46+, scanpy 1.10+, vegan 2.6+
Before using code patterns, verify installed versions match. If versions differ:
packageVersion('<pkg>') then ?function_name to verify parametersIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Compare microbial diversity across my samples" → Calculate alpha diversity (within-sample richness/evenness) and beta diversity (between-sample dissimilarity) to test for community composition differences across groups.
phyloseq::estimate_richness() for alpha, phyloseq::ordinate() for betavegan::adonis2() for PERMANOVA testinglibrary(phyloseq)
library(vegan)
library(ggplot2)
seqtab <- readRDS('seqtab_nochim.rds')
taxa <- readRDS('taxa.rds')
metadata <- read.csv('sample_metadata.csv', row.names = 1)
ps <- phyloseq(otu_table(seqtab, taxa_are_rows = FALSE),
tax_table(taxa),
sample_data(metadata))
taxa_names(ps) <- paste0('ASV', seq(ntaxa(ps)))
# Calculate multiple metrics
alpha_div <- estimate_richness(ps, measures = c('Observed', 'Chao1', 'Shannon', 'Simpson'))
alpha_div$SampleID <- rownames(alpha_div)
alpha_div <- merge(alpha_div, sample_data(ps), by = 'row.names')
# Statistical test
kruskal.test(Shannon ~ Group, data = alpha_div)
# Pairwise comparisons
pairwise.wilcox.test(alpha_div$Shannon, alpha_div$Group, p.adjust.method = 'BH')
plot_richness(ps, x = 'Group', measures = c('Observed', 'Shannon')) +
geom_boxplot() +
theme_minimal()
# Custom plot
ggplot(alpha_div, aes(x = Group, y = Shannon, fill = Group)) +
geom_boxplot() +
geom_jitter(width = 0.2, alpha = 0.5) +
theme_minimal() +
labs(y = 'Shannon Diversity Index')
Goal: Calculate phylogenetic alpha diversity (Faith's PD) from ASV data by building a de novo phylogeny and summing branch lengths.
Approach: Align ASV sequences with DECIPHER, construct a neighbor-joining tree with phangorn, root at midpoint, and compute PD using picante.
library(picante)
# Requires phylogenetic tree in phyloseq object
# Build tree from ASV sequences
library(DECIPHER)
library(phangorn)
seqs <- refseq(ps)
alignment <- AlignSeqs(seqs, anchor = NA)
phang_align <- phyDat(as(alignment, 'matrix'), type = 'DNA')
dm <- dist.ml(phang_align)
tree <- NJ(dm)
tree <- midpoint(tree)
phy_tree(ps) <- tree
# Calculate Faith's PD
otu_mat <- as.matrix(t(otu_table(ps)))
faith_pd <- pd(otu_mat, phy_tree(ps), include.root = TRUE)
alpha_div$PD <- faith_pd$PD
# Check if sequencing depth is adequate
rarecurve_data <- vegan::rarecurve(t(otu_table(ps)), step = 100, sample = min(sample_sums(ps)))
# ggplot version with ggrare (install from GitHub)
# devtools::install_github('gauravsk/ranacapa')
library(ranacapa)
p_rare <- ggrare(ps, step = 100, color = 'Group', se = FALSE)
p_rare + theme_minimal() + labs(title = 'Rarefaction Curves')
# Check sequencing depth
sample_sums(ps)
# Rarefy to minimum depth
ps_rarefied <- rarefy_even_depth(ps, sample.size = min(sample_sums(ps)),
rngseed = 42, replace = FALSE)
# Calculate distance matrices
bray <- phyloseq::distance(ps, method = 'bray') # Bray-Curtis
jaccard <- phyloseq::distance(ps, method = 'jaccard') # Jaccard
unifrac <- UniFrac(ps, weighted = TRUE) # Weighted UniFrac (requires tree)
# Ordination
ord_bray <- ordinate(ps, method = 'PCoA', distance = bray)
# Plot
plot_ordination(ps, ord_bray, color = 'Group') +
stat_ellipse(level = 0.95) +
theme_minimal()
# Test for group differences
metadata <- data.frame(sample_data(ps))
permanova_result <- adonis2(bray ~ Group, data = metadata, permutations = 999)
permanova_result
# With covariates
adonis2(bray ~ Group + Age + Sex, data = metadata, permutations = 999)
# Test homogeneity of dispersions (assumption of PERMANOVA)
beta_disp <- betadisper(bray, metadata$Group)
permutest(beta_disp)
plot(beta_disp)
ord_nmds <- ordinate(ps, method = 'NMDS', distance = bray)
# Check stress
ord_nmds$stress # Should be < 0.2
plot_ordination(ps, ord_nmds, color = 'Group') +
theme_minimal()
| Metric | Type | Considers Abundance | Phylogeny |
|---|---|---|---|
| Bray-Curtis | Quantitative | Yes | No |
| Jaccard | Binary | No | No |
| UniFrac (unweighted) | Binary | No | Yes |
| UniFrac (weighted) | Quantitative | Yes | Yes |