Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Differential abundance testing for microbiome data using compositionally-aware methods like ALDEx2, ANCOM-BC2, and MaAsLin2. Use when identifying taxa that differ between experimental groups while accounting for the compositional nature of microbiome data.
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Reference examples tested with: DESeq2 1.42+, ggplot2 3.5+, phyloseq 1.46+, scanpy 1.10+
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.
"Find which taxa differ between my groups" → Identify differentially abundant taxa between experimental conditions using compositionally-aware methods that account for the relative nature of microbiome data.
ALDEx2::aldex() for CLR-transformed Welch's t-testANCOMBC::ancombc2() for bias-corrected log-linear modelsMaaslin2::Maaslin2() for multivariable associationMicrobiome data is compositional - abundances are relative, not absolute. Standard tests (t-test, DESeq2) can give false positives.
Goal: Identify differentially abundant taxa between groups using a compositionally-aware statistical framework.
Approach: Apply CLR transformation with Monte Carlo sampling on the OTU table, run Welch's t-test per taxon, and filter by FDR-corrected p-value and effect size.
library(ALDEx2)
library(phyloseq)
ps <- readRDS('phyloseq_object.rds')
otu <- as.data.frame(otu_table(ps))
if (!taxa_are_rows(ps)) otu <- t(otu)
# Define groups
groups <- sample_data(ps)$Group
# Run ALDEx2 (CLR transformation + Welch's t-test)
aldex_results <- aldex(otu, groups, mc.samples = 128, test = 'welch',
effect = TRUE, include.sample.summary = FALSE)
# Filter significant
sig_aldex <- aldex_results[aldex_results$we.eBH < 0.05 & abs(aldex_results$effect) > 1, ]
# Volcano-like plot
aldex.plot(aldex_results, type = 'MW', test = 'welch')
library(ANCOMBC)
# Run ANCOM-BC2 with sensitivity analysis
ancom_result <- ancombc2(data = ps, fix_formula = 'Group',
p_adj_method = 'BH', pseudo_sens = TRUE,
prv_cut = 0.1, lib_cut = 1000,
group = 'Group', struc_zero = TRUE)
# Extract results (includes sensitivity analysis)
res_df <- ancom_result$res
# Primary results
sig_ancom <- res_df[res_df$diff_Group == TRUE, ]
# Check sensitivity (passed_ss = passed sensitivity analysis)
robust_hits <- res_df[res_df$diff_Group == TRUE & res_df$passed_ss_Group == TRUE, ]
library(Maaslin2)
# Prepare data
features <- as.data.frame(t(otu_table(ps)))
metadata <- as.data.frame(sample_data(ps))
# Run MaAsLin2
maaslin_results <- Maaslin2(
input_data = features,
input_metadata = metadata,
output = 'maaslin2_output',
fixed_effects = 'Group',
normalization = 'CLR',
transform = 'NONE',
analysis_method = 'LM'
)
# Results in maaslin2_output/all_results.tsv
sig_maaslin <- maaslin_results$results[maaslin_results$results$qval < 0.05, ]
library(DESeq2)
library(phyloseq)
# Convert to DESeq2 (use geometric mean of poscounts)
ps_deseq <- ps
ps_deseq <- prune_samples(sample_sums(ps_deseq) > 1000, ps_deseq)
dds <- phyloseq_to_deseq2(ps_deseq, ~ Group)
dds <- DESeq(dds, test = 'Wald', fitType = 'parametric', sfType = 'poscounts')
res <- results(dds, alpha = 0.05)
sig_deseq <- res[which(res$padj < 0.05 & abs(res$log2FoldChange) > 1), ]
library(ggplot2)
# Volcano plot from ALDEx2
ggplot(aldex_results, aes(x = effect, y = -log10(we.eBH))) +
geom_point(aes(color = we.eBH < 0.05 & abs(effect) > 1), alpha = 0.6) +
geom_hline(yintercept = -log10(0.05), linetype = 'dashed') +
geom_vline(xintercept = c(-1, 1), linetype = 'dashed') +
scale_color_manual(values = c('grey', 'red')) +
theme_minimal() +
labs(x = 'Effect Size', y = '-log10(Adjusted P-value)')
| Method | Handles | Covariates | Speed | Notes |
|---|---|---|---|---|
| ALDEx2 | Compositionality | Limited | Slow | Best for simple designs |
| ANCOM-BC2 | Compositionality, zeros, sensitivity | Yes | Medium | Recommended for complex designs |
| MaAsLin2 | Compositionality | Yes | Fast | Good for longitudinal |
| DESeq2 | Sparsity (less ideal) | Yes | Fast | Use with caution for microbiome |
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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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