Model comparison with the AIC
Spindle length dataset download
[1]:
import warnings
import pandas as pd
import numpy as np
import numba
import scipy.optimize
import scipy.stats as st
import bebi103
import iqplot
import bokeh.io
bokeh.io.output_notebook()
We have previously introduced the Akaike information criterion. Here, we will demonstrate its use in model comparison and the mechanics of how to calculated it.
As a reminder, for a set of parameters \(\theta\) with MLE \(\theta^*\) and a model with log-likelihood \(\ell(\theta;\text{data})\), the AIC is given by
\begin{align} \text{AIC} = -2\ell(\theta^*;\text{data}) + 2p, \end{align}
where \(p\) is the number of free parameters in a model. The Akaike weight of model \(i\) in a collection of models is
\begin{align} w_i = \frac{\mathrm{e}^{-(\text{AIC}_i - \text{AIC}_\mathrm{max})/2}}{\sum_j\mathrm{e}^{-(\text{AIC}_j - \text{AIC}_\mathrm{max})/2}}. \end{align}
To begin, we will use the AIC to compare a single Negative Binomial model to a mixture of two Negative Binomials for smFISH data from Singer, et al.
AIC for mRNA counts
Let us now compare the single Negative Binomial to the mixture model for mRNA counts. We again need our functions for computing the MLE and computing the log-likelihood from previous lessons.
[2]:
def log_like_iid_nbinom(params, n):
"""Log likelihood for i.i.d. NBinom measurements, parametrized
by alpha, b=1/beta."""
alpha, b = params
if alpha <= 0 or b <= 0:
return -np.inf
return np.sum(st.nbinom.logpmf(n, alpha, 1/(1+b)))
def mle_iid_nbinom(n):
"""Perform maximum likelihood estimates for parameters for i.i.d.
NBinom measurements, parametrized by alpha, b=1/beta"""
with warnings.catch_warnings():
warnings.simplefilter("ignore")
res = scipy.optimize.minimize(
fun=lambda params, n: -log_like_iid_nbinom(params, n),
x0=np.array([3, 3]),
args=(n,),
method='Powell'
)
if res.success:
return res.x
else:
raise RuntimeError('Convergence failed with message', res.message)
def initial_guess_mix(n, w_guess):
"""Generate initial guess for mixture model."""
n_low = n[n < np.percentile(n, 100*w_guess)]
n_high = n[n >= np.percentile(n, 100*w_guess)]
alpha1, b1 = mle_iid_nbinom(n_low)
alpha2, b2 = mle_iid_nbinom(n_high)
return alpha1, b1, alpha2, b2
def log_like_mix(alpha1, b1, alpha2, b2, w, n):
"""Log-likeihood of binary Negative Binomial mixture model."""
# Fix nonidentifieability be enforcing values of w
if w < 0 or w > 1:
return -np.inf
# Physical bounds on parameters
if alpha1 < 0 or alpha2 < 0 or b1 < 0 or b2 < 0:
return -np.inf
logx1 = st.nbinom.logpmf(n, alpha1, 1/(1+b1))
logx2 = st.nbinom.logpmf(n, alpha2, 1/(1+b2))
# Multipliers for log-sum-exp
lse_coeffs = np.tile([w, 1-w], [len(n), 1]).transpose()
# log-likelihood for each measurement
log_likes = scipy.special.logsumexp(np.vstack([logx1, logx2]), axis=0, b=lse_coeffs)
return np.sum(log_likes)
def mle_mix(n, w_guess):
"""Obtain MLE estimate for parameters for binary mixture
of Negative Binomials."""
with warnings.catch_warnings():
warnings.simplefilter("ignore")
res = scipy.optimize.minimize(
fun=lambda params, n: -log_like_mix(*params, n),
x0=[*initial_guess_mix(n, w_guess), w_guess],
args=(n,),
method='Powell',
tol=1e-6,
)
if res.success:
return res.x
else:
raise RuntimeError('Convergence failed with message', res.message)
Now we can load in the data and compute the MLEs for each of the four genes.
[3]:
# Load in data
df = pd.read_csv("../data/singer_transcript_counts.csv", comment="#")
df_mle = pd.DataFrame(index=['alpha', 'b', 'alpha1', 'b1', 'alpha2', 'b2', 'w'])
for gene in df:
n = df['Nanog'].values
# Single Negative Binomial MLE
alpha, b = mle_iid_nbinom(df[gene].values)
# Mixture model MLE
alpha1, b1, alpha2, b2, w = mle_mix(df[gene].values, 0.2)
# Store results in data frame
df_mle[gene] = [alpha, b, alpha1, b1, alpha2, b2, w]
# Take a look
df_mle
[3]:
Rex1 | Rest | Nanog | Prdm14 | |
---|---|---|---|---|
alpha | 1.634562 | 4.530335 | 1.263097 | 0.552886 |
b | 84.680915 | 16.543054 | 69.347842 | 8.200636 |
alpha1 | 3.497010 | 2.786599 | 0.834853 | 2.385858 |
b1 | 4.104915 | 12.395709 | 66.534676 | 4.747278 |
alpha2 | 5.089624 | 6.683424 | 4.127551 | 0.558672 |
b2 | 31.810372 | 11.953266 | 28.132831 | 4.872748 |
w | 0.160422 | 0.108772 | 0.466650 | 0.210606 |
For each of the two models, we can compute the log likelihood evaluated at the MLEs for the parameters.
[4]:
for gene in df:
ell = log_like_iid_nbinom(
(df_mle.loc["alpha", gene], df_mle.loc["b", gene]), df[gene].values
)
df_mle.loc["log_like_single", gene] = ell
ell_mix = log_like_mix(
*df_mle.loc[["alpha1", 'b1', 'alpha2', 'b2', 'w'], gene].values,
df[gene].values,
)
df_mle.loc["log_like_mix", gene] = ell_mix
# Take a look
df_mle
[4]:
Rex1 | Rest | Nanog | Prdm14 | |
---|---|---|---|---|
alpha | 1.634562 | 4.530335 | 1.263097 | 0.552886 |
b | 84.680915 | 16.543054 | 69.347842 | 8.200636 |
alpha1 | 3.497010 | 2.786599 | 0.834853 | 2.385858 |
b1 | 4.104915 | 12.395709 | 66.534676 | 4.747278 |
alpha2 | 5.089624 | 6.683424 | 4.127551 | 0.558672 |
b2 | 31.810372 | 11.953266 | 28.132831 | 4.872748 |
w | 0.160422 | 0.108772 | 0.466650 | 0.210606 |
log_like_single | -1638.678482 | -1376.748398 | -1524.928918 | -713.091587 |
log_like_mix | -1590.353744 | -1372.108896 | -1512.444549 | -712.702876 |
We can already see a very large difference between the log likelihood evaluated at the MLE for Rex1, but not much difference for Prdm14. The mixture morel has \(p = 5\) parameters, while the single Negative Binomial model has \(p = 2\). With these numbers, we can compute the AIC and then also the Akaike weights.
[5]:
for gene in df:
df_mle.loc['AIC_single', gene] = -2 * (df_mle.loc['log_like_single', gene] - 2)
df_mle.loc['AIC_mix', gene] = -2 * (df_mle.loc['log_like_mix', gene] - 5)
# Take a look
df_mle
[5]:
Rex1 | Rest | Nanog | Prdm14 | |
---|---|---|---|---|
alpha | 1.634562 | 4.530335 | 1.263097 | 0.552886 |
b | 84.680915 | 16.543054 | 69.347842 | 8.200636 |
alpha1 | 3.497010 | 2.786599 | 0.834853 | 2.385858 |
b1 | 4.104915 | 12.395709 | 66.534676 | 4.747278 |
alpha2 | 5.089624 | 6.683424 | 4.127551 | 0.558672 |
b2 | 31.810372 | 11.953266 | 28.132831 | 4.872748 |
w | 0.160422 | 0.108772 | 0.466650 | 0.210606 |
log_like_single | -1638.678482 | -1376.748398 | -1524.928918 | -713.091587 |
log_like_mix | -1590.353744 | -1372.108896 | -1512.444549 | -712.702876 |
AIC_single | 3281.356963 | 2757.496797 | 3053.857837 | 1430.183173 |
AIC_mix | 3190.707487 | 2754.217792 | 3034.889098 | 1435.405751 |
Finally, we can compute the Akaike weight for the mixture model (the weight for the single Negative Binomial model is \(1-w_\mathrm{mix}\)).
[6]:
for gene in df:
AIC_max = max(df_mle.loc[['AIC_single', 'AIC_mix'], gene])
numerator = np.exp(-(df_mle.loc['AIC_single', gene] - AIC_max)/2)
denominator = numerator + np.exp(-(df_mle.loc['AIC_mix', gene] - AIC_max)/2)
df_mle.loc['w_single', gene] = numerator / denominator
# Take a look
df_mle
[6]:
Rex1 | Rest | Nanog | Prdm14 | |
---|---|---|---|---|
alpha | 1.634562e+00 | 4.530335 | 1.263097 | 0.552886 |
b | 8.468092e+01 | 16.543054 | 69.347842 | 8.200636 |
alpha1 | 3.497010e+00 | 2.786599 | 0.834853 | 2.385858 |
b1 | 4.104915e+00 | 12.395709 | 66.534676 | 4.747278 |
alpha2 | 5.089624e+00 | 6.683424 | 4.127551 | 0.558672 |
b2 | 3.181037e+01 | 11.953266 | 28.132831 | 4.872748 |
w | 1.604216e-01 | 0.108772 | 0.466650 | 0.210606 |
log_like_single | -1.638678e+03 | -1376.748398 | -1524.928918 | -713.091587 |
log_like_mix | -1.590354e+03 | -1372.108896 | -1512.444549 | -712.702876 |
AIC_single | 3.281357e+03 | 2757.496797 | 3053.857837 | 1430.183173 |
AIC_mix | 3.190707e+03 | 2754.217792 | 3034.889098 | 1435.405751 |
w_single | 2.068790e-20 | 0.162533 | 0.000076 | 0.931585 |
In looking at the Akaike weight for the mixture (1 – w_single
), is it clear that the mixture model is strongly preferred for Rex1 and Nanog. There is not strong preference for Rest, and a preference for the single Negative Binomial model for Prdm14. Reminding ourselves of the ECDFs, this makes sense.
[7]:
genes = ["Nanog", "Prdm14", "Rest", "Rex1"]
plots = [
iqplot.ecdf(
data=df[gene].values,
q=gene,
x_axis_label="mRNA count",
title=gene,
frame_height=150,
frame_width=200,
)
for gene in genes
]
bokeh.io.show(bokeh.layouts.gridplot(plots, ncols=2))
Rex1 clearly is bimodal, and Nanog appears to have a second inflection point where the ECDF reaches a value of about 0.4, which is what we see in the MLE estimates in the mixture model. Rest and Prdm14 both appear to be unimodal, agreeing with what we saw with the AIC analysis.
Note that this underscores something we’ve been stressing all term. You should do good exploratory data analysis first, and the EDA often tells much of the story!
Caveat
Remember, though, that we did not take into account that the measurements of the four genes were done in the same cells. We modeled that when we presented the mixture models at the beginning of this lesson. The analysis of a more complicated model with MLE proved to be out of reach due to computational difficulty. So, we should not make strong conclusions about what the relative quality of the mixture of single Negative Binomial models mean in this context. We will address these kinds of modeling issues next term.
AIC for the spindle model
We can do a similar analysis for the two competing models for mitotic spindle size. We need our functions from earlier.
[8]:
def theor_spindle_length(gamma, phi, d):
"""Compute spindle length using mathematical model"""
return gamma * d / np.cbrt(1 + (gamma * d / phi)**3)
def log_likelihood(params, d, ell):
"""Log likelihood of spindle length model."""
gamma, phi, sigma = params
if gamma <= 0 or gamma > 1 or phi <= 0:
return -np.inf
mu = theor_spindle_length(gamma, phi, d)
return np.sum(st.norm.logpdf(ell, mu, sigma))
def spindle_mle(d, ell):
"""Compute MLE for parameters in spindle length model."""
with warnings.catch_warnings():
warnings.simplefilter("ignore")
res = scipy.optimize.minimize(
fun=lambda params, d, ell: -log_likelihood(params, d, ell),
x0=np.array([0.5, 35, 5]),
args=(d, ell),
method='Powell'
)
if res.success:
return res.x
else:
raise RuntimeError('Convergence failed with message', res.message)
We can now perform MLE to get the parameters for each model and store them in a Pandas Series for convenience.
[9]:
df = pd.read_csv("../data/good_invitro_droplet_data.csv", comment="#")
mle_1 = df["Spindle Length (um)"].apply([np.mean, np.std]).values
mle_2 = spindle_mle(
df["Droplet Diameter (um)"].values, df["Spindle Length (um)"].values
)
s = pd.Series(
index=["phi_1", "sigma_1", "gamma", "phi_2", "sigma_2"],
data=np.concatenate((mle_1, mle_2)),
)
Next, we can compute the log likelihood evaluated at the MLE.
[10]:
s["log_like_1"] = st.norm.logpdf(df["Spindle Length (um)"], s["phi_1"], s["sigma_1"]).sum()
s["log_like_2"] = log_likelihood(
s[["gamma", "phi_2", "sigma_2"]],
df["Droplet Diameter (um)"],
df["Spindle Length (um)"],
)
s
[10]:
phi_1 32.864030
sigma_1 4.788240
gamma 0.860475
phi_2 38.231250
sigma_2 3.753422
log_like_1 -1999.517925
log_like_2 -1837.158982
dtype: float64
The log likeihood for model 2, with spindle size depending on droplet diameter, is much greater than for model 1. And now we can compute the AIC,noting that there are two parameters for model 1 and three for model 2.
[11]:
s["AIC_1"] = -2 * (s['log_like_1'] - 2)
s["AIC_2"] = -2 * (s['log_like_2'] - 3)
s
[11]:
phi_1 32.864030
sigma_1 4.788240
gamma 0.860475
phi_2 38.231250
sigma_2 3.753422
log_like_1 -1999.517925
log_like_2 -1837.158982
AIC_1 4003.035850
AIC_2 3680.317964
dtype: float64
There is a massive disparity in the AICs, so we know that model 2 is strongly preferred. Nonetheless, we can compute the Akaike weight for model 1 to compare.
[12]:
AIC_max = max(s[['AIC_1', 'AIC_2']])
numerator = np.exp(-(s.loc['AIC_1'] - AIC_max)/2)
denominator = numerator + np.exp(-(s['AIC_2'] - AIC_max)/2)
s['w_single'] = numerator / denominator
s
[12]:
phi_1 3.286403e+01
sigma_1 4.788240e+00
gamma 8.604745e-01
phi_2 3.823125e+01
sigma_2 3.753422e+00
log_like_1 -1.999518e+03
log_like_2 -1.837159e+03
AIC_1 4.003036e+03
AIC_2 3.680318e+03
w_single 8.369539e-71
dtype: float64
Model 1 is completely out of the question, with a tiny Akaike weight!
Computing environment
[13]:
%load_ext watermark
%watermark -v -p numpy,pandas,scipy,bokeh,iqplot,bebi103,jupyterlab
Python implementation: CPython
Python version : 3.11.4
IPython version : 8.12.2
numpy : 1.24.3
pandas : 2.0.3
scipy : 1.11.1
bokeh : 3.2.1
iqplot : 0.3.4
bebi103 : 0.1.15
jupyterlab: 4.0.5