Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
The English summary is being prepared. Showing the original description.
Build tissue and condition-specific metabolic models using GIMME, iMAT, and INIT algorithms with expression data constraints. Create models that reflect cell-type specific metabolism. Use when building tissue-specific metabolic models or integrating transcriptomics with FBA.
The English summary is being prepared. Showing the original description.
See how to installReview the instructions the agent will receive before you install.
Reference examples tested with: COBRApy 0.29+, numpy 1.26+, pandas 2.2+
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.
"Build a tissue-specific metabolic model from my expression data" → Constrain a generic genome-scale model using transcriptomics data to produce a context-specific model reflecting the active metabolism of a particular tissue or condition, using GIMME, iMAT, or INIT algorithms.
cobra model manipulation (COBRApy)Goal: Build a tissue-specific metabolic model by integrating transcriptomics data with a generic genome-scale model, retaining only metabolically active reactions.
Approach: Map gene expression values to reactions, penalize flux through lowly-expressed reactions while maintaining minimum biomass production, and remove inactive reactions to produce a context-specific model.
import cobra
import numpy as np
def gimme(model, expression_data, threshold=0.25, required_growth=0.1):
'''Gene Inactivity Moderated by Metabolism and Expression (GIMME)
Creates context-specific model by:
1. Penalizing flux through lowly-expressed reactions
2. Requiring minimum biomass production
Args:
expression_data: dict mapping gene_id -> expression value
threshold: Expression percentile below which genes are inactive
0.25 = bottom 25% considered inactive
required_growth: Minimum growth rate to maintain
Returns:
Context-specific model with inactive reactions constrained
'''
# Calculate expression threshold
values = list(expression_data.values())
cutoff = np.percentile(values, threshold * 100)
# Identify lowly-expressed genes
low_expressed = {g for g, v in expression_data.items() if v < cutoff}
# Create context model
context_model = model.copy()
# Set minimum growth constraint
context_model.reactions.get_by_id('Biomass_Ecoli_core').lower_bound = required_growth
# Minimize flux through reactions with low-expressed genes
for rxn in context_model.reactions:
genes = {g.id for g in rxn.genes}
if genes and genes.issubset(low_expressed):
# This reaction is likely inactive - constrain it
rxn.upper_bound = min(rxn.upper_bound, 1.0)
rxn.lower_bound = max(rxn.lower_bound, -1.0)
return context_model
def imat(model, expression_data, high_threshold=0.75, low_threshold=0.25):
'''Integrative Metabolic Analysis Tool (iMAT)
Maximizes agreement between flux activity and expression:
- Highly expressed reactions should carry flux
- Lowly expressed reactions should have zero flux
More sophisticated than GIMME - uses MILP optimization.
'''
from cobra import Reaction
# Classify reactions by expression
high_expr_rxns = []
low_expr_rxns = []
for rxn in model.reactions:
if rxn.genes:
# Aggregate gene expression (use max for OR, min for AND)
gene_expr = [expression_data.get(g.id, 0.5) for g in rxn.genes]
rxn_expr = max(gene_expr) # Simplified OR logic
if rxn_expr > np.percentile(list(expression_data.values()), high_threshold * 100):
high_expr_rxns.append(rxn.id)
elif rxn_expr < np.percentile(list(expression_data.values()), low_threshold * 100):
low_expr_rxns.append(rxn.id)
# Create MILP to maximize consistent reactions
# This is a simplified version - full iMAT uses binary variables
context_model = model.copy()
# Force flux through highly expressed reactions
for rxn_id in high_expr_rxns:
rxn = context_model.reactions.get_by_id(rxn_id)
rxn.lower_bound = max(rxn.lower_bound, 0.01)
# Constrain lowly expressed reactions
for rxn_id in low_expr_rxns:
rxn = context_model.reactions.get_by_id(rxn_id)
rxn.upper_bound = min(rxn.upper_bound, 0.1)
rxn.lower_bound = max(rxn.lower_bound, -0.1)
return context_model, high_expr_rxns, low_expr_rxns
def load_expression_data(filepath, gene_col='gene_id', expr_col='TPM'):
'''Load and normalize expression data
Accepts:
- RNA-seq counts (TPM, FPKM)
- Microarray intensities
- Proteomics abundances
Returns dict mapping gene_id -> normalized expression
'''
import pandas as pd
df = pd.read_csv(filepath)
# Log-transform if needed (high dynamic range)
expr = df[expr_col].values
if expr.max() / expr.mean() > 100:
expr = np.log2(expr + 1)
# Normalize to 0-1 range
expr_norm = (expr - expr.min()) / (expr.max() - expr.min())
return dict(zip(df[gene_col], expr_norm))
def aggregate_gene_expression(model, expression_data, method='max'):
'''Map gene expression to reactions
Methods:
- 'max': Use maximum gene expression (OR logic)
- 'min': Use minimum gene expression (AND logic)
- 'mean': Average across genes
For GPR: (A and B) or C
- min(A, B) for the complex
- max(complex, C) for the alternatives
'''
rxn_expression = {}
for rxn in model.reactions:
if not rxn.genes:
rxn_expression[rxn.id] = 0.5 # Default for non-enzymatic
continue
gene_expr = [expression_data.get(g.id, 0.5) for g in rxn.genes]
if method == 'max':
rxn_expression[rxn.id] = max(gene_expr)
elif method == 'min':
rxn_expression[rxn.id] = min(gene_expr)
else:
rxn_expression[rxn.id] = np.mean(gene_expr)
return rxn_expression
def create_tissue_model(generic_model, gtex_expression, tissue='liver'):
'''Create tissue-specific model from GTEx expression data
GTEx provides median TPM for 54 human tissues.
Download from: https://gtexportal.org/home/datasets
'''
import pandas as pd
# Load GTEx median expression
gtex = pd.read_csv(gtex_expression, sep='\t')
# Extract tissue column
tissue_col = [c for c in gtex.columns if tissue.lower() in c.lower()][0]
expression = dict(zip(gtex['gene_id'], gtex[tissue_col]))
# Apply GIMME
tissue_model = gimme(generic_model, expression, threshold=0.25)
return tissue_model
def validate_context_model(original, context, expression_data):
'''Compare original and context-specific models
Checks:
1. Growth capability maintained
2. Inactive reactions reduced
3. Active reactions maintained
'''
# Growth comparison
orig_growth = original.optimize().objective_value
context_growth = context.optimize().objective_value
# Count constrained reactions
constrained = 0
for rxn in context.reactions:
orig_rxn = original.reactions.get_by_id(rxn.id)
if rxn.upper_bound < orig_rxn.upper_bound:
constrained += 1
return {
'original_growth': orig_growth,
'context_growth': context_growth,
'growth_ratio': context_growth / orig_growth,
'constrained_reactions': constrained,
'total_reactions': len(context.reactions)
}
No reviews yet. Tell others what you thought.
No login needed. Share how it worked for you, ask a question, or note where it did not run.
No comments yet. Be the first to write one.
Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
The English summary is being prepared. Showing the original description.
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.
The English summary is being prepared. Showing the original description.
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.
The English summary is being prepared. Showing the original description.
Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
The English summary is being prepared. Showing the original description.
ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
The English summary is being prepared. Showing the original description.
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.
The English summary is being prepared. Showing the original description.