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用PyMC3进行贝叶斯统计分析(代码+实例)
發布時間:2024/7/23
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用PyMC3进行贝叶斯统计分析(代码+实例)
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問題類型1:參數估計
真實值是否等于X?
給出數據,對于參數,可能的值的概率分布是多少?
例子1:拋硬幣問題
硬幣扔了n次,正面朝上是h次。
參數問題
想知道 p 的可能性。給定 n 扔的次數和 h 正面朝上次數,p 的值很可能接近 0.5,比如說在 [0.48,0.52]?
說明
- 參數的先驗信念:p~Uniform(0,1)
- 似然函數:data~Bernoulli(p)
可視化數據:
def plot_coins():fig = plt.figure()ax = fig.add_subplot(1,1,1)ax.bar(list(Counter(tosses).keys()), list(Counter(tosses).values()))ax.set_xticks([0, 1])ax.set_xticklabels(['tails', 'heads'])ax.set_ylim(0, 20)ax.set_yticks(np.arange(0, 21, 5)) return figfig = plot_coins() plt.show()?建立模型:
with pm.Model() as coin_model:# Specify prior using Uniform object.p_prior = pm.Uniform('p', 0, 1) # Specify likelihood using Bernoulli object.like = pm.Bernoulli('likelihood', p=p_prior, observed=tosses) # "observed=data" is key for likelihood.MCMC Inference Button?
with coin_model:step = pm.Metropolis() # focus on this, the Inference Button:coin_trace = pm.sample(2000, step=step)結果:
pm.traceplot(coin_trace) plt.show() pm.plot_posterior(coin_trace[100:], color='#87ceeb',rope=[0.48,0.52], point_estimate='mean', ref_val=0.5) plt.show()?
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例子2:化學活性問題
我有一個新開發的分子X; X在阻止流感方面的效果有多好?
實驗
- 測試X的濃度范圍,測量流感活動
- 根據實驗結果計算 IC50:導致病毒復制率減半的X濃度。
數據
import numpy as np import pandas as pdchem_data = [(0.00080, 99), (0.00800, 91), (0.08000, 89), (0.40000, 89), (0.80000, 79), (1.60000, 61), (4.00000, 39), (8.00000, 25), (80.00000, 4)]chem_df = pd.DataFrame(chem_data) chem_df.columns = ['concentration', 'activity'] chem_df['concentration_log'] = chem_df['concentration'].apply(lambda x:np.log10(x))參數問題
給出數據,化學品的IC50 值是多少, 以及其周圍的不確定性?
說明
可視化數據
def plot_chemical_data(log=True):fig = plt.figure(figsize=(10,6))ax = fig.add_subplot(1,1,1) if log:ax.scatter(x=chem_df['concentration_log'], y=chem_df['activity'])ax.set_xlabel('log10(concentration (mM))', fontsize=20) else:ax.scatter(x=chem_df['concentration'], y=chem_df['activity'])ax.set_xlabel('concentration (mM)', fontsize=20)ax.set_xticklabels([int(i) for i in ax.get_xticks()], fontsize=18)ax.set_yticklabels([int(i) for i in ax.get_yticks()], fontsize=18)plt.hlines(y=50, xmin=min(ax.get_xlim()), xmax=max(ax.get_xlim()), linestyles='--',) return figfig = plot_chemical_data(log=True) plt.show() with pm.Model() as ic50_model:beta = pm.HalfNormal('beta', sd=100**2)ic50_log10 = pm.Flat('IC50_log10') # Flat prior# MATH WITH DISTRIBUTION OBJECTS!measurements = beta / (1 + np.exp(chem_df['concentration_log'].values - ic50_log10))y_like = pm.Normal('y_like', mu=measurements, observed=chem_df['activity']) ic50 = pm.Deterministic('IC50', np.power(10, ic50_log10))# MCMC Inference Button with ic50_model:step = pm.Metropolis()ic50_trace = pm.sample(10000, step=step) pm.traceplot(ic50_trace[2000:], varnames=['IC50_log10', 'IC50']) # live: sample from step 2000 onwards. plt.show()?
pm.plot_posterior(ic50_trace[4000:], varnames=['IC50'], color='#87ceeb', point_estimate='mean') plt.show()?該化學物質的IC50在約 [2mM,2.4mM](95%HPD)
問題類型2:實驗組之間的比較
實驗組和對照組的不同
例子1:藥物IQ問題
藥物治療是否影響 IQ Scores
數據(包括對照實驗數據)
drug = [ 99., 110., 107., 104., 省略] placebo = [ 95., 105., 103., 99., 省略]def ECDF(data):x = np.sort(data)y = np.cumsum(x) / np.sum(x) return x, ydef plot_drug():fig = plt.figure()ax = fig.add_subplot(1,1,1)x_drug, y_drug = ECDF(drug)ax.plot(x_drug, y_drug, label='drug, n={0}'.format(len(drug)))x_placebo, y_placebo = ECDF(placebo)ax.plot(x_placebo, y_placebo, label='placebo, n={0}'.format(len(placebo)))ax.legend()ax.set_xlabel('IQ Score')ax.set_ylabel('Cumulative Frequency')ax.hlines(0.5, ax.get_xlim()[0], ax.get_xlim()[1], linestyle='--') return figfig = plot_drug() plt.show()?
from scipy.stats import ttest_indttest_ind(drug, placebo)# Ttest_indResult(statistic=2.2806701634329549, pvalue=0.025011500508647616)?
實驗
- 隨機將參與者分配給兩個實驗組:
- +drug vs. -drug
- 測量每個參與者的 IQ Scores
說明
建模:?
y_vals = np.concatenate([drug, placebo]) labels = ['drug'] * len(drug) + ['placebo'] * len(placebo)data = pd.DataFrame([y_vals, labels]).T data.columns = ['IQ', 'treatment'] with pm.Model() as kruschke_model: # Linking Distribution Objects together is done by # passing objects into other objects' parameters.mu_drug = pm.Normal('mu_drug', mu=0, sd=100**2)mu_placebo = pm.Normal('mu_placebo', mu=0, sd=100**2)sigma_drug = pm.HalfCauchy('sigma_drug', beta=100)sigma_placebo = pm.HalfCauchy('sigma_placebo', beta=100)nu = pm.Exponential('nu', lam=1/29) + 1drug_like = pm.StudentT('drug', nu=nu, mu=mu_drug, sd=sigma_drug, observed=drug)placebo_like = pm.StudentT('placebo', nu=nu, mu=mu_placebo, sd=sigma_placebo, observed=placebo)diff_means = pm.Deterministic('diff_means', mu_drug - mu_placebo)pooled_sd = pm.Deterministic('pooled_sd', np.sqrt(np.power(sigma_drug, 2) + np.power(sigma_placebo, 2) / 2))effect_size = pm.Deterministic('effect_size', diff_means / pooled_sd)with kruschke_model:kruschke_trace = pm.sample(10000, step=pm.Metropolis())?結果:
pm.traceplot(kruschke_trace[2000:], varnames=['mu_drug', 'mu_placebo']) plt.show()?
pm.plot_posterior(kruschke_trace[2000:], color='#87ceeb',varnames=['mu_drug', 'mu_placebo', 'diff_means']) plt.show()?
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