labarchive-integration
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cobrapy
Constraint-based metabolic modeling (COBRA). FBA, FVA, gene knockouts, flux sampling, SBML models, for systems biology and metabolic engineering analysis.
Full skill instructions
COBRApy is a Python library for constraint-based reconstruction and analysis (COBRA) of metabolic models, essential for systems biology research. Work with genome-scale metabolic models, perform computational simulations of cellular metabolism, conduct metabolic engineering analyses, and predict phenotypic behaviors.
COBRApy provides comprehensive tools organized into several key areas:
Load existing models from repositories or files:
from cobra.io import load_model
# Load bundled test models
model = load_model("textbook") # E. coli core model
model = load_model("ecoli") # Full E. coli model
model = load_model("salmonella")
# Load from files
from cobra.io import read_sbml_model, load_json_model, load_yaml_model
model = read_sbml_model("path/to/model.xml")
model = load_json_model("path/to/model.json")
model = load_yaml_model("path/to/model.yml")
Save models in various formats:
from cobra.io import write_sbml_model, save_json_model, save_yaml_model
write_sbml_model(model, "output.xml") # Preferred format
save_json_model(model, "output.json") # For Escher compatibility
save_yaml_model(model, "output.yml") # Human-readable
Access and inspect model components:
# Access components
model.reactions # DictList of all reactions
model.metabolites # DictList of all metabolites
model.genes # DictList of all genes
# Get specific items by ID or index
reaction = model.reactions.get_by_id("PFK")
metabolite = model.metabolites[0]
# Inspect properties
print(reaction.reaction) # Stoichiometric equation
print(reaction.bounds) # Flux constraints
print(reaction.gene_reaction_rule) # GPR logic
print(metabolite.formula) # Chemical formula
print(metabolite.compartment) # Cellular location
Perform standard FBA simulation:
# Basic optimization
solution = model.optimize()
print(f"Objective value: {solution.objective_value}")
print(f"Status: {solution.status}")
# Access fluxes
print(solution.fluxes["PFK"])
print(solution.fluxes.head())
# Fast optimization (objective value only)
objective_value = model.slim_optimize()
# Change objective
model.objective = "ATPM"
solution = model.optimize()
Parsimonious FBA (minimize total flux):
from cobra.flux_analysis import pfba
solution = pfba(model)
Geometric FBA (find central solution):
from cobra.flux_analysis import geometric_fba
solution = geometric_fba(model)
Determine flux ranges for all reactions:
from cobra.flux_analysis import flux_variability_analysis
# Standard FVA
fva_result = flux_variability_analysis(model)
# FVA at 90% optimality
fva_result = flux_variability_analysis(model, fraction_of_optimum=0.9)
# Loopless FVA (eliminates thermodynamically infeasible loops)
fva_result = flux_variability_analysis(model, loopless=True)
# FVA for specific reactions
fva_result = flux_variability_analysis(
model,
reaction_list=["PFK", "FBA", "PGI"]
)
Perform knockout analyses:
from cobra.flux_analysis import (
single_gene_deletion,
single_reaction_deletion,
double_gene_deletion,
double_reaction_deletion
)
# Single deletions
gene_results = single_gene_deletion(model)
reaction_results = single_reaction_deletion(model)
# Double deletions (uses multiprocessing)
double_gene_results = double_gene_deletion(
model,
processes=4 # Number of CPU cores
)
# Manual knockout using context manager
with model:
model.genes.get_by_id("b0008").knock_out()
solution = model.optimize()
print(f"Growth after knockout: {solution.objective_value}")
# Model automatically reverts after context exit
Manage growth medium:
# View current medium
print(model.medium)
# Modify medium (must reassign entire dict)
medium = model.medium
medium["EX_glc__D_e"] = 10.0 # Set glucose uptake
medium["EX_o2_e"] = 0.0 # Anaerobic conditions
model.medium = medium
# Calculate minimal media
from cobra.medium import minimal_medium
# Minimize total import flux
min_medium = minimal_medium(model, minimize_components=False)
# Minimize number of components (uses MILP, slower)
min_medium = minimal_medium(
model,
minimize_components=True,
open_exchanges=True
)
Sample the feasible flux space:
from cobra.sampling import sample
# Sample using OptGP (default, supports parallel processing)
samples = sample(model, n=1000, method="optgp", processes=4)
# Sample using ACHR
samples = sample(model, n=1000, method="achr")
# Validate samples
from cobra.sampling import OptGPSampler
sampler = OptGPSampler(model, processes=4)
sampler.sample(1000)
validation = sampler.validate(sampler.samples)
print(validation.value_counts()) # Should be all 'v' for valid
Calculate phenotype phase planes:
from cobra.flux_analysis import production_envelope
# Standard production envelope
envelope = production_envelope(
model,
reactions=["EX_glc__D_e", "EX_o2_e"],
objective="EX_ac_e" # Acetate production
)
# With carbon yield
envelope = production_envelope(
model,
reactions=["EX_glc__D_e", "EX_o2_e"],
carbon_sources="EX_glc__D_e"
)
# Visualize (use matplotlib or pandas plotting)
import matplotlib.pyplot as plt
envelope.plot(x="EX_glc__D_e", y="EX_o2_e", kind="scatter")
plt.show()
Add reactions to make models feasible:
from cobra.flux_analysis import gapfill
# Prepare universal model with candidate reactions
universal = load_model("universal")
# Perform gapfilling
with model:
# Remove reactions to create gaps for demonstration
model.remove_reactions([model.reactions.PGI])
# Find reactions needed
solution = gapfill(model, universal)
print(f"Reactions to add: {solution}")
Build models from scratch:
from cobra import Model, Reaction, Metabolite
# Create model
model = Model("my_model")
# Create metabolites
atp_c = Metabolite("atp_c", formula="C10H12N5O13P3",
name="ATP", compartment="c")
adp_c = Metabolite("adp_c", formula="C10H12N5O10P2",
name="ADP", compartment="c")
pi_c = Metabolite("pi_c", formula="HO4P",
name="Phosphate", compartment="c")
# Create reaction
reaction = Reaction("ATPASE")
reaction.name = "ATP hydrolysis"
reaction.subsystem = "Energy"
reaction.lower_bound = 0.0
reaction.upper_bound = 1000.0
# Add metabolites with stoichiometry
reaction.add_metabolites({
atp_c: -1.0,
adp_c: 1.0,
pi_c: 1.0
})
# Add gene-reaction rule
reaction.gene_reaction_rule = "(gene1 and gene2) or gene3"
# Add to model
model.add_reactions([reaction])
# Add boundary reactions
model.add_boundary(atp_c, type="exchange")
model.add_boundary(adp_c, type="demand")
# Set objective
model.objective = "ATPASE"
from cobra.io import load_model
# Load model
model = load_model("ecoli")
# Run FBA
solution = model.optimize()
print(f"Growth rate: {solution.objective_value:.3f} /h")
# Show active pathways
print(solution.fluxes[solution.fluxes.abs() > 1e-6])
from cobra.io import load_model
from cobra.flux_analysis import single_gene_deletion
# Load model
model = load_model("ecoli")
# Perform single gene deletions
results = single_gene_deletion(model)
# Find essential genes (growth < threshold)
essential_genes = results[results["growth"] < 0.01]
print(f"Found {len(essential_genes)} essential genes")
# Find genes with minimal impact
neutral_genes = results[results["growth"] > 0.9 * solution.objective_value]
from cobra.io import load_model
from cobra.medium import minimal_medium
# Load model
model = load_model("ecoli")
# Calculate minimal medium for 50% of max growth
target_growth = model.slim_optimize() * 0.5
min_medium = minimal_medium(
model,
target_growth,
minimize_components=True
)
print(f"Minimal medium components: {len(min_medium)}")
print(min_medium)
from cobra.io import load_model
from cobra.flux_analysis import flux_variability_analysis
from cobra.sampling import sample
# Load model
model = load_model("ecoli")
# First check flux ranges at optimality
fva = flux_variability_analysis(model, fraction_of_optimum=1.0)
# For reactions with large ranges, sample to understand distribution
samples = sample(model, n=1000)
# Analyze specific reaction
reaction_id = "PFK"
import matplotlib.pyplot as plt
samples[reaction_id].hist(bins=50)
plt.xlabel(f"Flux through {reaction_id}")
plt.ylabel("Frequency")
plt.show()
Use context managers to make temporary modifications:
# Model remains unchanged outside context
with model:
# Temporarily change objective
model.objective = "ATPM"
# Temporarily modify bounds
model.reactions.EX_glc__D_e.lower_bound = -5.0
# Temporarily knock out genes
model.genes.b0008.knock_out()
# Optimize with changes
solution = model.optimize()
print(f"Modified growth: {solution.objective_value}")
# All changes automatically reverted
solution = model.optimize()
print(f"Original growth: {solution.objective_value}")
Models use DictList objects for reactions, metabolites, and genes - behaving like both lists and dictionaries:
# Access by index
first_reaction = model.reactions[0]
# Access by ID
pfk = model.reactions.get_by_id("PFK")
# Query methods
atp_reactions = model.reactions.query("atp")
Reaction bounds define feasible flux ranges:
lower_bound = 0, upper_bound > 0lower_bound < 0, upper_bound > 0.bounds to avoid inconsistenciesBoolean logic linking genes to reactions:
# AND logic (both required)
reaction.gene_reaction_rule = "gene1 and gene2"
# OR logic (either sufficient)
reaction.gene_reaction_rule = "gene1 or gene2"
# Complex logic
reaction.gene_reaction_rule = "(gene1 and gene2) or (gene3 and gene4)"
Special reactions representing metabolite import/export:
EX_ by conventionmodel.medium dictionarymodel.slim_optimize() to ensure feasibilityoptimal indicates successful solveInfeasible solutions: Check medium constraints, reaction bounds, and model consistency
Slow optimization: Try different solvers (GLPK, CPLEX, Gurobi) via model.solver
Unbounded solutions: Verify exchange reactions have appropriate upper bounds
Import errors: Ensure correct file format and valid SBML identifiers
For detailed workflows and API patterns, refer to:
references/workflows.md - Comprehensive step-by-step workflow examplesreferences/api_quick_reference.md - Common function signatures and patternsOfficial documentation: https://cobrapy.readthedocs.io/en/latest/
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