Negative multinomial distribution

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Negative multinomial distribution

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Notation	$\textrm{NM}(k_0,\,p)$
Parameters	k₀ ∈ N₀ — the number of failures before the experiment is stopped, p ∈ R^m — m-vector of “success” probabilities, p₀ = 1 − (p₁+…+p_m) — the probability of a “failure”.
Support	$k_i \in \{0,1,2,\ldots\}, 1\leq i\leq m$
PDF	$\Gamma\!\left(\sum_{i=0}^m{k_i}\right)\frac{p_0^{k_0}}{\Gamma(k_0)} \prod_{i=1}^m{\frac{p_i^{k_i}}{k_i!}},$ where Γ(x) is the Gamma function.
Mean	$\tfrac{k_0}{p_0}\,p$
Variance	$\tfrac{k_0}{p_0^2}\,pp' + \tfrac{k_0}{p_0}\,\operatorname{diag}(p)$
CF	$\bigg(\frac{p_0}{1 - p'e^{it}}\bigg)^{\!k_0}$

In probability theory and statistics, the negative multinomial distribution is a generalization of the negative binomial distribution (NB(r, p)) to more than two outcomes.^[1]

Suppose we have an experiment that generates m+1≥2 possible outcomes, {X₀,…,X_m}, each occurring with non-negative probabilities {p₀,…,p_m} respectively. If sampling proceeded until n observations were made, then {X₀,…,X_m} would have been multinomially distributed. However, if the experiment is stopped once X₀ reaches the predetermined value k₀, then the distribution of the m-tuple {X₁,…,X_m} is negative multinomial.

Contents

1 Negative multinomial distribution example
2 Parameter estimation
3 Related distributions
4 References
5 Further reading

Negative multinomial distribution example

The table below shows the an example of 400 Melanoma (skin cancer) Patients where the Type and Site of the cancer are recorded for each subject.

Type	Site			Totals
Type	Head and Neck	Trunk	Extremities	Totals
Hutchinson's melanomic freckle	22	2	10	34
Superficial	16	54	115	185
Nodular	19	33	73	125
Indeterminant	11	17	28	56
Column Totals	68	106	226	400

The sites (locations) of the cancer may be independent, but there may be positive dependencies of the type of cancer for a given location (site). For example, localized exposure to radiation implies that elevated level of one type of cancer (at a given location) may indicate higher level of another cancer type at the same location. The Negative Multinomial distribution may be used to model the sites cancer rates and help measure some of the cancer type dependencies within each location.

If $x_{i,j}$ denote the cancer rates for each site ( $0\leq i \leq 2$ ) and each type of cancer ( $0\leq j \leq 3$ ), for a fixed site ( $i_0$ ) the cancer rates are independent Negative Multinomial distributed random variables. That is, for each column index (site) the column-vector X has the following distribution:

$X=\{X_1, X_2, X_3\} \sim NM(k_0,\{p_1,p_2,p_3\})$ .

Different columns in the table (sites) are considered to be different instances of the random multinomially distributed vector, X. Then we have the following estimates of expected counts (frequencies of cancer):

$\hat{\mu}_{i,j} = \frac{x_{i,.}\times x_{.,j}}{x_{.,.}}$

$x_{i,.} = \sum_{j=0}^{3}{x_{i,j}}$

$x_{.,j} = \sum_{i=0}^{2}{x_{i,j}}$

$x_{.,.} = \sum_{i=0}^{2}\sum_{j=0}^{3}{{x_{i,j}}}$

Example: $\hat{\mu}_{1,1} = \frac{x_{1,.}\times x_{.,1}}{x_{.,.}}=\frac{34\times 68}{400}=5.78$

For the first site (Head and Neck, j=0), suppose that $X=\left \{X_1=5, X_2=1, X_3=5\right \}$ and $X \sim NM(k_0=10, \{p_1=0.2, p_2=0.1, p_3=0.2 \})$ . Then:

$p_0 = 1 - \sum_{i=1}^3{p_i}=0.5$

$NM(X|k_0,\{p_1, p_2, p_3\})= 0.00465585119998784$

$cov[X_1,X_3] = \frac{10 \times 0.2 \times 0.2}{0.5^2}=1.6$

$\mu_2=\frac{k_0 p_2}{p_0} = \frac{10\times 0.1}{0.5}=2.0$

$\mu_3=\frac{k_0 p_3}{p_0} = \frac{10\times 0.2}{0.5}=4.0$

$corr[X_2,X_3] = \left (\frac{\mu_2 \times \mu_3}{(k_0+\mu_2)(k_0+\mu_3)} \right )^{\frac{1}{2}}$ and therefore, $corr[X_2,X_3] = \left (\frac{2 \times 4}{(10+2)(10+4)} \right )^{\frac{1}{2}} = 0.21821789023599242.$

Notice that the pair-wise NM correlations are always positive, whereas the correlations between multinomial counts are always negative. As the parameter $k_0$ increases, the paired correlations tend to zero! Thus, for large $k_0$ , the Negative Multinomial counts $X_i$ behave as independent Poisson random variables with respect to their means $\left ( \mu_i= k_0\frac{p_i}{p_0}\right )$ .

The marginal distribution of each of the $X_i$ variables is negative binomial, as the $X_i$ count (considered as success) is measured against all the other outcomes (failure). But jointly, the distribution of $X=\{X_1,\cdots,X_m\}$ is negative multinomial, i.e., $X \sim NM(k_0,\{p_1,\cdots,p_m\})$ .

Parameter estimation

Estimation of the mean (expected) frequency counts ( $\mu_j$ ) of each outcome ( $X_j$ ) using maximum likelihood is possible. If we have a single observation vector $\{x_1, \cdots,x_m\}$ , then $\hat{\mu}_i=x_i.$ If we have several observation vectors, like in this case we have the cancer type frequencies for 3 different sites, then the MLE estimates of the mean counts are $\hat{\mu}_j=\frac{x_{j,.}}{I}$ , where $0\leq j \leq J$ is the cancer-type index and the summation is over the number of observed (sampled) vectors (I). For the cancer data above, we have the following MLE estimates for the expectations for the frequency counts:

Hutchinson's melanomic freckle type of cancer ( $X_0$ ) is $\hat{\mu}_0 = 34/3=11.33$ .

Superficial type of cancer ( $X_1$ ) is $\hat{\mu}_1 = 185/3=61.67$ .

Nodular type of cancer ( $X_2$ ) is $\hat{\mu}_2 = 125/3=41.67$ .

Indeterminant type of cancer ( $X_3$ ) is $\hat{\mu}_3 = 56/3=18.67$ .

There is no MLE estimate for the NM $k_0$ parameter.^[1]^[2] However, there are approximate protocols for estimating the $k_0$ parameter using the chi-squared goodness of fit statistic. In the usual chi-squared statistic:

$\Chi^2 = \sum_i{\frac{(x_i-\mu_i)^2}{\mu_i}}$ , we can replace the expected-means ( $\mu_i$ ) by their estimates, $\hat{\mu_i}$ , and replace denominators by the corresponding negative multinomial variances. Then we get the following test statistic for negative multinomial distributed data:

$\Chi^2(k_0) = \sum_{i}{\frac{(x_i-\hat{\mu_i})^2}{\hat{\mu_i} \left (1+ \frac{\hat{\mu_i}}{k_0} \right )}}$ .

Next, we can estimate the $k_0$ parameter by varying the values of $k_0$ in the expression $\Chi^2(k_0)$ and matching the values of this statistic with the corresponding asymptotic chi-squared distribution. The following protocol summarizes these steps using the cancer data above.

DF: The degree of freedom for the Chi-squared distribution in this case is:

df = (# rows – 1)(# columns – 1) = (3-1)*(4-1) = 6

Median: The median of a chi-squared random variable with 6 df is 5.261948.

Mean Counts Estimates: The mean counts estimates ( $\mu_j$ ) for the 4 different cancer types are:

$\hat{\mu}_1 = 185/3=61.67$ ; $\hat{\mu}_2 = 125/3=41.67$ ; and $\hat{\mu}_3 = 56/3=18.67$ .

Thus, we can solve the equation above $\Chi^2(k_0) = 5.261948$ for the single variable of interest -- the unknown parameter $k_0$ . In the cancer example, suppose $x=\{x_1=5,x_2=1,x_3=5\}$ . Then, the solution is an asymptotic chi-squared distribution driven estimate of the parameter $k_0$ .

$\Chi^2(k_0) = \sum_{i=1}^3{\frac{(x_i-\hat{\mu_i})^2}{\hat{\mu_i} \left (1+ \frac{\hat{\mu_i}}{k_0} \right )}}$ .

$\Chi^2(k_0) = \frac{(5-61.67)^2}{61.67(1+61.67/k_0)}+\frac{(1-41.67)^2}{41.67(1+41.67/k_0)}+\frac{(5-18.67)^2}{18.67(1+18.67/k_0)}=5.261948.$ Solving this equation for $k_0$ provides the desired estimate for the last parameter.

Mathematica provides 3 distinct ( $k_0$ ) solutions to this equation: {50.5466, -21.5204, 2.40461}. Since $k_0>0$ there are 2 candidate solutions.

Estimates of probabilities: Assume $k_0=2$ and $\frac{\mu_i}{k_0}p_0=p_i$ , then:

$\frac{61.67}{k_0}p_0=31p_0=p_1$

$20p_0=p_2$

$9p_0=p_3$

Hence, $1-p_0=p_1+p_2+p_3=60p_0$ , and $p_0=\frac{1}{61}$ , $p_1=\frac{31}{61}$ , $p_2=\frac{20}{61}$ and $p_3=\frac{9}{61}$ .

Therefore, the best model distribution for the observed sample $x=\{x_1=5,x_2=1,x_3=5\}$ is $X \sim NM\left (2, \left \{\frac{31}{61}, \frac{20}{61},\frac{9}{61}\right\} \right ).$

Related distributions

References

^ ^a ^b Le Gall, F. The modes of a negative multinomial distribution, Statistics & Probability Letters, Volume 76, Issue 6, 15 March 2006, Pages 619-624, ISSN 0167-7152, 10.1016/j.spl.2005.09.009.
^ Zelterman, Daniel (2002). Advanced log-linear models using SAS. SAS Publishing. p. 196. ISBN 978-1-59047-080-0.

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