跳到正文
cccskills
免费在 GitHub 公开

bio-microbiome-diversity-analysis

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.

中文简介正在准备中。当前显示原文说明。

实测评分 未实测

查看安装方法

包含的文件(3)

  • SKILL.md5.5 KB
  • examples/diversity_analysis.R2.7 KB
  • usage-guide.md3.0 KB

SKILL.md(原文)

安装前可以查看交给 AI 代理的指令内容。

Version Compatibility

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:

  • R: packageVersion('<pkg>') then ?function_name to verify parameters

If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.

Diversity Analysis

"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.

  • R: phyloseq::estimate_richness() for alpha, phyloseq::ordinate() for beta
  • R: vegan::adonis2() for PERMANOVA testing

Create phyloseq Object

library(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)))

Alpha Diversity

# 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')

Alpha Diversity Plots

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')

Faith's Phylogenetic Diversity

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

Rarefaction Curves

# 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')

Rarefaction

# 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)

Beta Diversity

# 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()

PERMANOVA

# 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)

Beta Dispersion

# Test homogeneity of dispersions (assumption of PERMANOVA)
beta_disp <- betadisper(bray, metadata$Group)
permutest(beta_disp)
plot(beta_disp)

NMDS Ordination

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()

Distance Metrics Comparison

MetricTypeConsiders AbundancePhylogeny
Bray-CurtisQuantitativeYesNo
JaccardBinaryNoNo
UniFrac (unweighted)BinaryNoYes
UniFrac (weighted)QuantitativeYesYes

Related Skills

  • amplicon-processing - Generate ASV table
  • differential-abundance - Identify taxa driving differences
  • data-visualization/ggplot2-fundamentals - Custom diversity plots
  • ecological-genomics/biodiversity-metrics - Hill number coverage-based rarefaction for ecological data
  • ecological-genomics/community-ecology - Constrained ordination and indicator species

评价

还没有评价。欢迎分享你的使用感受。

评论

无需登录即可发表。欢迎分享使用感受、提问,或说明在哪些环境下无法运行。

还没有评论。来写第一条吧。

提交后会立即公开。请勿填写邮箱、电话等个人信息。URL 最多 2 个。

0 / 1000 字

此表单受 reCAPTCHA 保护,适用 Google 的隐私权政策和服务条款。

同一仓库的技能

Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.

中文简介正在准备中。当前显示原文说明。

BioTender-max/awesome-bio-agent-skills2042026年7月2日 更新

alphafold

免费

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.

中文简介正在准备中。当前显示原文说明。

BioTender-max/awesome-bio-agent-skills2042026年7月2日 更新

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.

中文简介正在准备中。当前显示原文说明。

BioTender-max/awesome-bio-agent-skills2042026年7月2日 更新

Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.

中文简介正在准备中。当前显示原文说明。

BioTender-max/awesome-bio-agent-skills2042026年7月2日 更新

atac-seq

免费

ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.

中文简介正在准备中。当前显示原文说明。

BioTender-max/awesome-bio-agent-skills2042026年7月2日 更新

bindcraft

免费

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.

中文简介正在准备中。当前显示原文说明。

BioTender-max/awesome-bio-agent-skills2042026年7月2日 更新

查看 BioTender-max 的全部技能

报告此技能的问题