single-cell/metabolite-communication/SKILL.md
Analyze metabolite-mediated cell-cell communication using MeboCost for metabolic signaling inference between cell types. Predict metabolite secretion and sensing patterns from scRNA-seq data. Use when studying metabolic crosstalk between cell populations or metabolite-receptor interactions.
npx skillsauth add GPTomics/bioSkills bio-single-cell-metabolite-communicationInstall this skill globally with one command. Works with Claude Code, Cursor, and Windsurf.
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Reference examples tested with: matplotlib 3.8+, scanpy 1.10+
Before using code patterns, verify installed versions match. If versions differ:
pip show <package> then help(module.function) to check signaturesIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Analyze metabolic crosstalk between cell types" -> Predict metabolite secretion-sensing interactions between cell populations based on enzyme and transporter expression patterns.
mebocost.MeboCost(adata, groupby='cell_type') -> run_mebocost()MeboCost infers metabolite-mediated communication by:
Goal: Infer metabolite-mediated cell-cell communication from scRNA-seq data by predicting which cell types secrete and sense specific metabolites.
Approach: Initialize a MeboCost object from an AnnData with cell type annotations, run permutation-based communication inference to score metabolite secretion-sensing interactions, then filter for statistically significant pairs.
import mebocost as mbc
import scanpy as sc
# Load scRNA-seq data
adata = sc.read_h5ad('adata.h5ad')
# Initialize MeboCost
mebo = mbc.create_obj(
adata=adata,
group_col='cell_type', # Cell type annotation column
species='human' # 'human' or 'mouse'
)
# Infer metabolite communication
mebo.infer_commu(
n_permutations=1000, # Permutations for significance testing
seed=42
)
# Get significant interactions
sig_interactions = mebo.commu_res[mebo.commu_res['pval'] < 0.05]
import scanpy as sc
def prepare_for_mebocost(adata, cell_type_col='cell_type', min_cells=50):
'''Prepare AnnData for MeboCost analysis
Requirements:
- Log-normalized expression (sc.pp.normalize_total, sc.pp.log1p)
- Cell type annotations
- Gene symbols (not Ensembl IDs)
'''
# Check normalization
if adata.X.max() > 50:
print('Warning: Data may not be log-normalized')
# Filter rare cell types
cell_counts = adata.obs[cell_type_col].value_counts()
valid_types = cell_counts[cell_counts >= min_cells].index
adata = adata[adata.obs[cell_type_col].isin(valid_types)].copy()
print(f'Cell types: {len(valid_types)}')
print(f'Cells: {adata.n_obs}')
return adata
def run_mebocost(adata, cell_type_col='cell_type', species='human'):
'''Run MeboCost metabolite communication analysis
Args:
adata: AnnData with log-normalized expression
cell_type_col: Column with cell type annotations
species: 'human' or 'mouse'
Returns:
MeboCost object with communication results
'''
import mebocost as mbc
# Create MeboCost object
mebo = mbc.create_obj(
adata=adata,
group_col=cell_type_col,
species=species
)
# Infer enzyme-metabolite-receptor communication
# n_permutations: Higher = more accurate p-values but slower
# 1000 is standard; use 100 for quick exploration
mebo.infer_commu(n_permutations=1000, seed=42)
return mebo
def analyze_metabolite_communication(mebo, pval_threshold=0.05):
'''Extract and summarize significant communications
Communication flow:
Sender cell -> Enzyme -> Metabolite -> Receptor -> Receiver cell
'''
results = mebo.commu_res.copy()
# Filter significant interactions
sig = results[results['pval'] < pval_threshold]
# Summary statistics
summary = {
'total_interactions': len(results),
'significant_interactions': len(sig),
'unique_metabolites': sig['metabolite'].nunique(),
'unique_sender_types': sig['sender'].nunique(),
'unique_receiver_types': sig['receiver'].nunique()
}
# Top metabolites by frequency
top_metabolites = sig['metabolite'].value_counts().head(10)
# Top sender-receiver pairs
sig['pair'] = sig['sender'] + ' -> ' + sig['receiver']
top_pairs = sig['pair'].value_counts().head(10)
return {
'summary': summary,
'top_metabolites': top_metabolites,
'top_pairs': top_pairs,
'significant_interactions': sig
}
def plot_communication_network(mebo, pval_threshold=0.05):
'''Plot metabolite communication network'''
import matplotlib.pyplot as plt
# Filter significant
sig = mebo.commu_res[mebo.commu_res['pval'] < pval_threshold]
# Aggregate by cell type pair
pair_counts = sig.groupby(['sender', 'receiver']).size().reset_index(name='count')
# Create chord diagram or heatmap
pivot = pair_counts.pivot(index='sender', columns='receiver', values='count')
pivot = pivot.fillna(0)
plt.figure(figsize=(10, 8))
plt.imshow(pivot.values, cmap='Reds')
plt.xticks(range(len(pivot.columns)), pivot.columns, rotation=45, ha='right')
plt.yticks(range(len(pivot.index)), pivot.index)
plt.colorbar(label='Number of interactions')
plt.xlabel('Receiver')
plt.ylabel('Sender')
plt.title('Metabolite Communication Network')
plt.tight_layout()
return plt.gcf()
def plot_metabolite_flow(mebo, metabolite, pval_threshold=0.05):
'''Visualize communication flow for specific metabolite'''
sig = mebo.commu_res[
(mebo.commu_res['metabolite'] == metabolite) &
(mebo.commu_res['pval'] < pval_threshold)
]
print(f'\n{metabolite} communication:')
for _, row in sig.iterrows():
print(f" {row['sender']} ({row['enzyme']}) -> "
f"{row['receiver']} ({row['receptor']})")
print(f" Score: {row['commu_score']:.3f}, p-value: {row['pval']:.4f}")
def compare_conditions(adata, condition_col, cell_type_col, species='human'):
'''Compare metabolite communication between conditions
Useful for:
- Tumor vs normal
- Treatment vs control
- Disease vs healthy
'''
import mebocost as mbc
conditions = adata.obs[condition_col].unique()
results = {}
for condition in conditions:
adata_subset = adata[adata.obs[condition_col] == condition].copy()
mebo = mbc.create_obj(
adata=adata_subset,
group_col=cell_type_col,
species=species
)
mebo.infer_commu(n_permutations=1000, seed=42)
results[condition] = mebo.commu_res
# Find differential communications
# Interactions significant in one condition but not another
return results
# MeboCost includes curated metabolite-receptor pairs
# Major categories:
METABOLITE_CATEGORIES = {
'amino_acids': ['Glutamine', 'Glutamate', 'Tryptophan', 'Arginine'],
'lipids': ['Prostaglandin E2', 'Leukotriene B4', 'Sphingosine-1-phosphate'],
'nucleotides': ['ATP', 'Adenosine', 'UDP'],
'vitamins': ['Retinoic acid', 'Vitamin D'],
'other': ['Lactate', 'Succinate', 'Itaconate']
}
def filter_by_category(results, category):
'''Filter results to specific metabolite category'''
metabolites = METABOLITE_CATEGORIES.get(category, [])
return results[results['metabolite'].isin(metabolites)]
tools
--- name: bio-phasing-imputation-foundations description: Frames the phasing/imputation pipeline before any tool runs: phasing and imputation are one Li-Stephens copying HMM (recombination is the transition, mutation the emission, the genetic map and Ne set the rates), imputation's honest output is a dosage with a self-estimated quality (INFO/R2/DR2) not a hard genotype, and the stages are ordered and each fails silently (QC, align build and strand to the panel, phase, impute per chromosome, fil
tools
Chooses the enrichment generation before any tool runs, mapping the input shape to a method class - a pre-selected gene list plus a background to over-representation analysis (ORA, hypergeometric), a ranked statistic for all genes to gene set enrichment (GSEA), a signed signaling topology to pathway-topology (SPIA) - then making the null explicit (competitive vs self-contained, gene vs subject sampling) and running a trustworthiness checklist (testable-gene universe, FDR, redundancy collapse, leading-edge check, version reporting). Covers why every clusterProfiler GSEA is the inter-gene-correlation-uncorrected competitive null, why the background not the gene list decides ORA significance, and why no method is universally best. Use when deciding ORA vs GSEA vs topology, which gene-set DB, whether a result is trustworthy, or which null a tool computes. For ORA see go-enrichment, GSEA see gsea, databases kegg-pathways/reactome-pathways/wikipathways; the ranking comes from differential-expression/de-results.
testing
End-to-end GWAS workflow from VCF to association results. Covers PLINK QC, population structure correction, and association testing for case-control or quantitative traits. Use when running genome-wide association studies.
development
Orchestrates the full path from differential expression results to redundancy-collapsed functional enrichment: choose ORA vs GSEA, convert gene IDs per method, run enrichGO/enrichKEGG/enrichPathway/enrichWP or gseGO/gseKEGG (clusterProfiler, ReactomePA, rWikiPathways), and visualize. Routes the ORA-vs-GSEA generation fork and the null/universe/reproducibility theory to pathway-analysis/enrichment-foundations. Use when a DESeq2/edgeR/limma result must become enriched GO terms, KEGG/Reactome/WikiPathways pathways, or a GSEA leading edge; when deciding whether a ranking exists for all genes (GSEA, named decreasing vector) or only a pre-selected list (ORA plus a defensible background universe); or when assembling DE-to-pathway end to end. The DE list and ranking statistic come from differential-expression/de-results; per-method nuance lives in the pathway-analysis skills.