Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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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.
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설치 방법 보기설치하기 전에 에이전트에게 전달되는 지시 내용을 확인할 수 있습니다.
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 |
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Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.
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AlphaFold2 / AlphaFold-Multimer structure prediction for validation and confidence scoring. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm2-sequence-scoring. For QC thresholds, use protein-design-qc.
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Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
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ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
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End-to-end binder design using BindCraft hallucination. Use this skill when: (1) Designing protein binders with built-in AF2 validation, (2) Running production-quality binder campaigns, (3) Using different design protocols (fast, default, slow), (4) Need joint backbone and sequence optimization, (5) Want high experimental success rate. For backbone-only generation, use rfdiffusion. For QC thresholds, use protein-qc. For tool selection guidance, use binder-design.
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