Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
日本語の概要は準備中です。原文の説明を表示しています。
Analyzes time-to-event data using Kaplan-Meier curves, log-rank tests, and Cox proportional hazards regression with lifelines. Builds survival models from clinical and omics features. Use when predicting patient survival or modeling time-to-event outcomes.
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Reference examples tested with: matplotlib 3.8+, 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.
"Analyze patient survival data" → Estimate survival curves (Kaplan-Meier), compare groups (log-rank test), and model time-to-event outcomes with Cox proportional hazards regression.
lifelines.KaplanMeierFitter(), lifelines.CoxPHFitter()Goal: Estimate and visualize the survival probability function from time-to-event data.
Approach: Fit a nonparametric Kaplan-Meier estimator to censored survival data and plot the step function.
from lifelines import KaplanMeierFitter
import matplotlib.pyplot as plt
kmf = KaplanMeierFitter()
# T: time to event or censoring
# E: event indicator (1=event occurred, 0=censored)
kmf.fit(T, event_observed=E)
# Plot survival curve
kmf.plot_survival_function()
plt.xlabel('Time (months)')
plt.ylabel('Survival probability')
plt.savefig('km_curve.png', dpi=150)
Goal: Test whether survival distributions differ significantly between risk groups.
Approach: Fit separate Kaplan-Meier curves per group, overlay them, and apply a log-rank test for statistical comparison.
from lifelines import KaplanMeierFitter
from lifelines.statistics import logrank_test
import matplotlib.pyplot as plt
fig, ax = plt.subplots(figsize=(8, 6))
for group, color in zip(['high', 'low'], ['red', 'blue']):
mask = df['risk_group'] == group
kmf = KaplanMeierFitter()
kmf.fit(df.loc[mask, 'time'], event_observed=df.loc[mask, 'event'], label=group)
kmf.plot_survival_function(ax=ax, color=color)
# Log-rank test
high = df[df['risk_group'] == 'high']
low = df[df['risk_group'] == 'low']
results = logrank_test(high['time'], low['time'], event_observed_A=high['event'], event_observed_B=low['event'])
print(f'Log-rank p-value: {results.p_value:.4e}')
ax.set_xlabel('Time (months)')
ax.set_ylabel('Survival probability')
ax.set_title(f'Log-rank p = {results.p_value:.4e}')
plt.savefig('km_comparison.png', dpi=150)
Goal: Model the effect of covariates on survival time using a semi-parametric hazard model.
Approach: Fit a Cox PH model to extract hazard ratios, confidence intervals, and a concordance index for predictive accuracy.
from lifelines import CoxPHFitter
# Prepare data: must have 'time' and 'event' columns
# Include covariates as additional columns
cph = CoxPHFitter()
cph.fit(df, duration_col='time', event_col='event')
# Summary with hazard ratios
cph.print_summary()
# Get hazard ratios as DataFrame
hr = cph.summary[['exp(coef)', 'exp(coef) lower 95%', 'exp(coef) upper 95%', 'p']]
print(hr)
# Concordance index (c-index): 0.5=random, 1.0=perfect
print(f'C-index: {cph.concordance_index_:.3f}')
Goal: Assess the independent prognostic value of clinical and molecular features in a single model.
Approach: Combine clinical covariates and gene expression values into a regularized Cox model to identify independently prognostic variables.
from lifelines import CoxPHFitter
import pandas as pd
# Combine clinical and omics features
cox_df = pd.DataFrame({
'time': meta['survival_months'],
'event': meta['vital_status'],
'age': meta['age'],
'stage': meta['stage_numeric'],
'GENE1': expr.loc['GENE1'],
'GENE2': expr.loc['GENE2']
})
cph = CoxPHFitter(penalizer=0.1) # L2 regularization for stability
cph.fit(cox_df, duration_col='time', event_col='event')
cph.print_summary()
Goal: Stratify patients into risk groups based on a fitted Cox model.
Approach: Compute partial hazard scores from model coefficients and split at the median to define high/low risk groups for downstream KM visualization.
# Partial hazard (risk score)
risk_scores = cph.predict_partial_hazard(cox_df)
# Median risk split for KM plot
df['risk_group'] = (risk_scores > risk_scores.median()).map({True: 'high', False: 'low'})
Goal: Verify that the proportional hazards assumption holds for all covariates.
Approach: Run the built-in Schoenfeld residual tests and inspect diagnostic plots for time-varying effects.
# Test PH assumption
cph.check_assumptions(df, p_value_threshold=0.05, show_plots=True)
Goal: Extract survival probability estimates at clinically meaningful time points.
Approach: Query the fitted Kaplan-Meier survival function at specific durations and report the median survival time.
# Survival probability at specific times
survival_probs = kmf.survival_function_at_times([12, 24, 60])
print(survival_probs)
# Median survival
print(f'Median survival: {kmf.median_survival_time_:.1f}')
Goal: Screen thousands of genes to identify those significantly associated with patient survival.
Approach: Fit univariate Cox models for each gene, extract hazard ratios and p-values, and rank candidates for multivariate modeling.
from lifelines import CoxPHFitter
import pandas as pd
# Univariate screening
results = []
for gene in expr.index[:1000]:
cox_df = pd.DataFrame({
'time': meta['survival_months'],
'event': meta['vital_status'],
'gene': expr.loc[gene]
})
cph = CoxPHFitter()
cph.fit(cox_df, duration_col='time', event_col='event')
results.append({
'gene': gene,
'hr': cph.hazard_ratios_['gene'],
'p': cph.summary.loc['gene', 'p']
})
results_df = pd.DataFrame(results)
sig_genes = results_df[results_df['p'] < 0.05].sort_values('p')
まだレビューはありません。使ってみた感想をお寄せください。
概要と使いどころ
Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
日本語の概要は準備中です。原文の説明を表示しています。
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.
日本語の概要は準備中です。原文の説明を表示しています。
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.
日本語の概要は準備中です。原文の説明を表示しています。
Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
日本語の概要は準備中です。原文の説明を表示しています。
ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
日本語の概要は準備中です。原文の説明を表示しています。
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.
日本語の概要は準備中です。原文の説明を表示しています。