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Article

Classical and Bayesian Inference on Finite Mixture of Exponentiated Kumaraswamy Gompertz and Exponentiated Kumaraswamy Fréchet Distributions under Progressive Type II Censoring with Applications

1
Department of Mathematical Sciences, College of Science, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh 11671, Saudi Arabia
2
Department of Mathematical Statistical, Faculty of Graduate Studies for Statistical Research, Cairo University, Giza 12613, Egypt
3
Department of Statistical, Faculty of Business Administration, Delta University for Science and Technology, Talkha 35712, Egypt
4
Department of Mathematics and Statistics, University of North Carolina, Wilmington, NC 27599, USA
5
Department of Statistics, Al-Azhar University, Cairo 11751, Egypt
*
Author to whom correspondence should be addressed.
Mathematics 2022, 10(9), 1496; https://doi.org/10.3390/math10091496
Submission received: 31 March 2022 / Revised: 24 April 2022 / Accepted: 26 April 2022 / Published: 30 April 2022
(This article belongs to the Section Probability and Statistics)

Abstract

:
A finite mixture of exponentiated Kumaraswamy Gompertz and exponentiated Kumaraswamy Fréchet is developed and discussed as a novel probability model. We study some useful structural properties of the proposed model. To estimate the model parameters under the classical method, we use the maximum likelihood estimation using a progressive type II censoring scheme. Under the Bayesian paradigm the estimation is carried out with gamma priors under a progressive type II censored samples with squared error loss function. To demonstrate the efficiency of the proposed model based on progressively type II censoring, a simulation study is carried out. Three actual data sets are used as an example, demonstrating that the suggested model in the new class fits better than the existing finite mixture models available in the literature.

1. Introduction

The literature on statistical distributions in the continuous domain can be supplemented in a number of ways. Adding one or more additional parameters to a baseline distribution, as proposed in [1], and it was subsequently developed by those who utilized a mixture of two normal distributions to fit a data set of crab measurements, which pioneered the use of finite mixture models in statistical research. Since then, mixture models have attracted a lot of interest, owing to the wide range of applications in which they are used. A non-exhaustive collection of references is provided below that utilized the concept of the several different mixing strategies to produce new probability models: [2,3,4]. Mixture distributions are a valuable statistical tool with more flexibility for analyzing and interpreting probabilistic called random occurrences in a potentially heterogeneous population. When modelling real-world data, it is typical to find that the data come from a mixed population that might comprise two or more distributions. In terms of applications of finite mixture models, there are plenty of areas, including but not limited to medical, economics, psychology, botany, fisheries research, life testing, and reliability, among others. Cluster analysis, latent structure models, empirical Bayes technique, and nonparametric density estimation are examples of indirect applications of such a process (finite mixture models).
Due to time constraints and several other constraints on data gathering such as constraints on resources, censoring in modeling lifetime data is very useful. Censoring occurs when specific lifetimes are only known for a subset of the individuals or units under study, but information on the remaining lifetimes is incomplete. There are various types of censoring schemes that exist in the literature, among which type II censoring is one of the most popular types. It is observed that type II censorship can be used to save time and money, i.e., it is economically profitable. However, when product lifetimes are extremely lengthy, the experimental period of a type II filtering life test can still be excessively long. Progressive type II censoring is a generalization of type II censoring that is beneficial when the loss of live test units at places other than the termination point is unavoidable. The type II gradually filtering approach has recently piqued the interest of statisticians, for example, see [5,6]. For further information on the theory, methodology, and applications of progressive filtering, see [7,8] for some recent comprehensive work in this context. Reference [9] developed a life test in which the experimenter may choose to organize the test units into various groups, each as an assembly of test units, and then run all of the test units simultaneously until the first failure in each group occurred. In this study, we conjecture that, scenarios regarding the analysis of lifetime data resembles to the case of progressive censoring. Therefore, in this study, we investigate a progressive type II censoring scheme, which is a generalization of the classical type II censoring scheme that allows living items to be removed during the experiment. For more information, see [10,11] and the references cited therein.
In the class of mixing distributions, among popular choices of a two-parameter probability model, the use of Kumaraswamy distribution as a baseline distribution under both the discrete and the continuous set-up have been well established in the literature. For example, the Kumaraswamy-G family by [12]; Kumaraswamy-beta generalized family by [13]; Kumaraswamy-Marshall–Olkin-G family by [14] and estimation of a three-component mixture of distributions via Bayesian and classical approaches is presented [15].
It is worth noting that while the additional parameter(s) increase the flexibility of a parent distribution, they come at a cost. With the addition of a new parameter or group of parameters, efficient estimation, and accurate interpretation of the model parameters for the proposed model become more cumbersome and at times quite difficult, for more information see [16]. In this article, we study a mixture between exponentiated Kumaraswamy Gompertz henceforth, in short (MEKGEKF) and exponentiated Kumaraswamy Fréchet distributions. We conjecture that the proposed mixture model will be useful in modeling behavior of various types of data for which, component-wise, either of the probability models might not provide an adequate fit and the data are obtained because of a progressively type II censoring.
The model described in this study generalizes several well-known distributions, including exponentiated Gompertz, exponentiated Kumaraswamy, exponentiated Fréchet, and exponentiated Fréchet distributions, among others. Furthermore, despite the fact that our MEKGEKF model contains 11 parameters, the density, cumulative, and probability functions, among others, do not have any non-manageable/intractable forms. This is beneficial since it makes it easier to obtain analytical and numerical results. This serves as a major motivation to carry out the present work. In addition, we investigated the MEKGEK model’s structural features and confirmed that all the suggested model’s formulas are basic and manageable given computational resources, for example, statistical computing software such as R/Mathematica/Matlab, etc.
The new MEKGEK model’s hazard function is versatile to suit all traditional forms, including increasing, decreasing, unimodal, and inverted bathtub shapes, among many others. As a result of their wide applicability in real life, these shapes are extremely essential. The actual data sets that are utilized to demonstrate the new MEKGEK model’s goodness-of-fit appears in support of the fact that it is indeed a very useful model. For the reasons stated above, we believe it is critical to investigate the MEKGEK distribution in more detail. We expect that this new mixed distribution will become a part of the applied researchers’ toolkit, and that it will be employed in a variety of contexts. The remainder of this article is structured as follows. Section 2 contains a mathematical description of the suggested model and some interesting structural aspects of the proposed model. Section 3 presents the maximum likelihood function of the suggested model under a progressively type II censoring. In Section 4, we present a general framework for Bayes estimation of the vector of parameters and posterior risk of the proposed model under squared error loss function under a progressively censored type II sampling scheme. In Section 5, we look at how to estimate the MEKGEKF distribution using both the classical and Bayesian paradigms, using a simulated study with various censoring schemes. In Section 6, three applications of the MEKGEKF distribution are given for illustrative purposes by modelling operation data on jobs made of iron sheet, Wire data, and the Australian athletes data set. Finally, some concluding remarks are presented in Section 7.

2. A Finite Mixture of Exponentiated Kumaraswamy Gompertz and Exponentiated Kumaraswamy Fréchet Model

The probability density function (PDF) of the exponentiated Kumaraswamy-G (henceforth, in short, EK) distributions was defined by several authors, such as [12,17,18], and has the following form of the density function
f ( x ) = a b c g ( x ) G a 1 ( x ) [ 1 G a ( x ) ] b 1 { [ 1 G a ( x ) ] b } c 1
where a , b , c are all positive parameters and x > 0, and G is the baseline distribution function.
The corresponding cumulative distribution function (CDF) is
F ( x ) = { 1 [ 1 G a ( x ) ] b } c ,   x > 0 .
A mixture model has the advantage of subsuming numerous other existing probability models, including the parent distribution, under specific parametric constraints. This feature is present in the suggested distribution that we have developed and studied in this paper. Taking G as a two parameter Gompertz distribution in (1), the PDF and CDF of exponentiated Kumaraswamy Gompertz (henceforth, in short, EKG) distributions are defined as follows:
f 1 ( x ) = a b c s e x p [ r x ( s r ) ( e x p ( r x ) 1 ) ] [ ( 1 e x p [ ( s r ) ( e x p ( r x ) 1 ) ] ) ] a 1 [ 1 ( 1 e x p [ ( s r ) ( e x p ( r x ) 1 ) ] ) a ] b 1 { 1 [ 1 ( 1 e x p [ ( s r ) ( e x p ( r x ) 1 ) ] ) a ] b } c 1 a ,   b ,   c ,   s ,   r > 0 ,   x > 0 ,  
and
F 1 ( x ) = { 1 [ 1 [ 1 e x p ( ( s r ) ( e x p ( r x ) 1 ) ) ] a ] b } c ,   x > 0 .
where s and r are the shape and scale parameters, respectively.
Similarly, taking G as a two parameter Fréchet distribution in (1), the PDF and CDF of exponentiated Kumaraswamy Fréchet (EKF) distributions is defined as
f 2 ( x ) = a b c s   [ r s ( x s ) r 1 e x p [ ( x s ) r ] ] [ e x p [ ( x s ) r ] ] a 1 [ 1 ( e x p [ ( x s ) r ] ) a ] b 1 { 1 [ 1 ( e x p [ ( x s ) r ] ) a ] b } c 1
and
F 2 ( x ) = { 1 [ 1 [ 1 e x p ( ( s r ) ( e x p ( r x ) 1 ) ) ] a ] b } c ,   x > 0 .
Next, the PDF of a two-component mixture of EKG and EKF (MEKGEKF) models with mixing proportions, ( p j ,   j = 1 , 2 ) is given as follows:
f ( x ) = p f 1 ( x ) + ( 1 p ) f 2 ( x )
in the mixing proportions must satisfy i = 1 2 p i = 1 , and p i 0 , and f 1 ( x ) , and f 2 ( x ) are defined in (2) and (3), and all the parameters are unknown. The associated CDF of the MEKGEKF model is given by:
F ( x ) = p F 1 ( x ) + ( 1 p ) F 2 ( x ) .
For q = 1 p of EKG and EKF distributions, a density function of mixture of two component densities with mixing proportions is ( p j ,   j = 1 , 2 ) , is given as follows:
f ( x ) = p a 1 b 1 c 1 s 1 e x p [ r 1 x ( s 1 r 1 ) ( e x p ( r 1 x ) 1 ) ] ( 1 e x p [ ( s r ) ( e x p ( r x ) 1 ) ] ) a 1 [ 1 ( 1 e x p [ ( s r ) ( e x p ( r x ) 1 ) ] ) a 1 ] b 1 1 [ 1 [ 1 [ 1 e x p ( ( s 1 r 1 ) ( e x p ( r 1 x ) 1 ) ) ] a 1 ] b 1 ] c 1 1 + q a 2 b 2 c 2 r 2 s 2 ( x s 2 ) r 2 1 e x p [ ( x s 2 ) r 2 ] [ 1 e x p ( ( x s 2 ) r 2 ) ] a 2 1 [ 1 [ 1 e x p ( ( x s 2 ) r 2 ) ] a 2 ] b 2 1 [ 1 [ 1 [ 1 e x p ( ( x s 2 ) r 2 ) ] a 2 ] b 2 ] c 2 1 ,   I ( 0 < x < ) .
The corresponding CDF is given by:
F ( x ) = p [ 1 [ 1 [ 1 e x p ( ( s 1 r 1 ) ( e x p ( r 1 x ) 1 ) ) ] a 1 ] b 1 ] c 1 + q [ 1 [ 1 [ e x p ( ( x s 2 ) r 2 ) ] a 2 ] b 2 ] c 2 .
The associated quantile function is given by:
Q j ( u ) = p { [ 1 ( 1 + l n ( s 1 r 1 ( l n ( 1 u ) ) ) r 1 ) 1 c 1 ] 1 b 1 } 1 a 1 + q { [ 1 ( s 2 ( l n ( u ) ) 1 r 2 ) 1 c 2 ] 1 b 2 } 1 a 2 .
Some representative plots of the PDF and the hrf corresponding to the density in (6) for varying values of the mixing parameter p = p are given in Figure 1.
From these plots, one can observe that the PDF of MEKGEKF distribution is unimodal and right skewed. Additionally, from the hrf plots it is observed that the hrf and the MEKGEKF distribution are decreasing, increasing, unimodal, and inverse bathtub shaped.

Laplace Transformation for MEKGEKF Model

Laplace transformation is a useful tool in probability and statistics. In this section, we begin our discussion by driving the Laplace transform for the proposed MEKGEKF model. From (6) of the MEKGEKF density, the associated Laplace transform will be
[ f ( u ) ] = [ p f 1 ( u ) + ( 1 p ) f 2 ( u ) ] = p f 1 ( u ) + ( 1 p ) f 2 ( u ) ,
where
f ( u ) = 0 e u t f ( t ) d t = 0 e u t f ( t ) d t = p 0 e u t f 1 ( t ) d t + ( 1 p ) 0 e u t f 2 ( t ) d t = p I 1 + ( 1 p ) I 2 ,
where
I 1 = f 1 ( u ) = 0 e u t f 1 ( t ) d t = 0 e u t { a b c s e x p [ r t ( s r ) ( e x p ( r t ) 1 ) ] [ ( 1 e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ) ] a 1 [ 1 ( 1 e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ) a ] b 1 { 1 [ 1 ( 1 e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ) a ] b } c 1 } d t ,
where, again,
I 2 = f 2 ( u ) = 0 e u t f 2 ( t ) d t = 0 e u t { a b c r s ( t s ) r 1 e x p [ ( t s ) r ] [ e x p ( ( t s ) r ) ] a 1 [ 1 [ 1 e x p ( ( t s ) r ) ] a ] b 1 [ 1 [ 1 [ 1 e x p ( ( t s ) r ) ] a ] b ] c 1 } d t = 0 e u t { a b c r s ( t s ) r 1 e x p [ ( t s ) r ] b 1 b 2 } d t ,
where
b 1 = [ e x p ( ( t s ) r ) ] a 1 [ 1 [ 1 e x p ( ( t s ) r ) ] a ] b 1 = [ e x p ( ( t s ) r ) ] a 1 j 1 = 0 ( b 1 j 1 ) [ e x p ( ( t s ) r ) ] j 1 a ,
b 2 = [ 1 [ 1 [ 1 e x p ( ( t s ) r ) ] a ] b ] c 1 = j 2 = 0 j 3 = 0 ( 1 ) j 2 + j 3 ( c 1 j 2 ) ( j 2 b j 3 ) [ e x p ( ( t s ) r ) ] j 3 a
Combining ( b 1 ) and ( b 2 ), we get:
I 2 = j 1 = 0 j 2 = 0 j 3 = 0 . ( 1 ) j 1 + j 2 + j 3 ( b 1 j 1 ) ( c 1 j 2 ) ( j 2 b j 3 ) [ ( e x p [ ( t s ) r ] ) ] j 3 a a b c r s 0 ( t s ) r 1 e ( t s ) r ( e ( t s ) r ) a ( j 1 + j 3 ) d t ,
Next, consider the following:
a 1 = ( 1 e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ) = j 1 = 0 . ( 1 ) j 1 ( a 1 j 1 ) ( e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ) j 1 ,  
a 2 = [ 1 ( 1 e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ) a ] b 1 = j 2 = 0 . ( 1 ) j 2 ( b 1 j 2 ) [ 1 ( e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ) ] j 2 a = j 2 = 0 . j 3 = 0 ( b 1 j 2 ) ( 1 ) j 2 + j 3 ( j 2 a j 3 ) [ e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ] j 3 ,
a 3 = { 1 [ 1 ( 1 e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ) a ] b } c 1 ( 1 e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ) = j 4 = 0 . ( c 1 j 4 ) ( 1 ) j 4 [ 1 [ e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ] j 3 a ] j 4 b = j 4 = 0 . ( c 1 j 4 ) ( 1 ) j 4 j 5 = 0 . ( b j 4 j 5 ) ( 1 ) j 5 ( 1 e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ) j 5 a = j 4 = 0 j 5 = 0 j 6 = 0 . ( 1 ) j 4 + j 5 + j 6 ( c 1 j 4 ) ( b j 4 j 5 ) ( j 5 a j 6 ) [ e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ] j 6 ,
Combing (10), (11), and (12) in (6), we get:
I 1 = a b c s j 1 = 0 j 2 = 0 j 3 = 0 . j 4 = 0 j 5 = 0 j 6 = 0 . ( 1 ) i = 1 6 j i . ( a 1 j 1 ) ( b 1 j 2 ) ( j 2 a j 3 ) ( c 1 j 4 ) ( j 4 b j 5 ) ( j 5 b j 6 ) 0 e u t [ e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ] [ e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ] j 1 + j 3 + j 6 d t , = M 1 0 e u t + r t [ e x p [ ( s r ) ( e x p ( r t ) 1 ) ] ] j 1 + j 3 + j 6 d t , = M 1 [ e s ( j 1 + j 3 + j 6 ) r E x p I n t e g r a l [ ( u r ) , s ( j 1 + j 3 + j 6 ) r ] ( s ( j 1 + j 3 + j 6 ) r ) 1 u r G a m m a ( 1 u r ) ] = M 3 ,
on using Mathematica.
Therefore,
I 2 = M 2 0 r s ( t s ) r 1 e x p [ ( t s ) r ( a j 3 + a j 1 ) ] d t = M 4
Observe that (13) is not available in closed form.
Therefore, the Laplace transformation for the MEKGEKF model is given by ( MEKGEKF   ) = p M 3 + ( 1 p ) M 4 , where M 3 and M 4 are given by (13) and (14), respectively.

3. Maximum Likelihood Estimation of MEKGEKF Distribution under Progressive Type II Censoring

Assume that n units are subjected to a life test at time 0, and that the experimenter determines the quantity m , the number of failures to be observed, ahead of time. Next, R 1 units are now randomly deleted from the remaining n-1 surviving units at the time of first failure; R 2 units from the remaining n 2 R 1 units are randomly deleted at the second failure. The test will continue until the mth failure has occurred. The remaining R m = n m R 1 R 2 R m 1 units are deleted at this time. R i and m are prefixed in this censoring scheme. The m failure times obtained from a progressive type II censoring scheme was arranged. Progressive type II censored ordered statistics are the names given to the values acquired as a result of this type of censoring scheme. This scheme reduces to a classical type II right censoring technique if R 1 = R 2 = = R m 1 = 0 , so that R m = n m . Additionally, if   R 1 = R 2 = = R m 1 = 0 , the progressively type II censoring method simplifies to the case of a complete sample (m = n, i.e., the case of no censoring).
Let x 1 , x 2 , , x m be a progressively type II censored sample, with the progressive censoring scheme ( R 1 , R 2 , , R m ) . Based on progressively type II censored samples obtained from the MEKGEKF distributions, from (6), the associated likelihood function will be:
L ( x _   | a 1 , a 2 ,   b 1 , b 2 , c 1 , c 2 , s 1 , s 2 , r 1 , r 2 , p , q ) i = 1 m { p a 1 b 1 c 1 s 1 e x p [ r 1 x i : m : n ( s 1 r 1 ) ( e x p ( r 1 x i : m : n ) 1 ) ] ( 1 e x p [ ( s r ) ( e x p ( r x i : m : n ) 1 ) ] ) a 1 [ 1 ( 1 e x p [ ( s r ) ( e x p ( r x i : m : n ) 1 ) ] ) a 1 ] b 1 1 [ 1 [ 1 [ 1 e x p ( ( s 1 r 1 ) ( e x p ( r 1 x i : m : n ) 1 ) ) ] a 1 ] b 1 ] c 1 1 . { ( 1 e x p [ ( s r 1 ) ( e x p ( r 1 x i : m : n ) 1 ) ] ) R i } + q a 2 b 2 c 2 r 2 s 2 ( x i : m : n s 2 ) r 2 1 e x p [ ( x i : m : n s 2 ) r 2 ] [ 1 e x p ( ( x i : m : n s 2 ) r 2 ) ] a 2 [ 1 [ 1 e x p ( ( x i : m : n s 2 ) r 2 ) ] a 2 ] b 2 1 [ 1 [ 1 [ 1 e x p ( ( x i : m : n s 2 ) r 2 ) ] a 2 ] b 2 ] c 2 1 . { ( e x p [ ( x i : m : n s 2 ) r 2 ] ) R i } } ,   i = 1 , 2 .
where k = n ( n 1 R 1 ) ( n 1 R 2 ) ( n m + 1 R 1 R m ) . Here, we get the log likelihood function without the constant term. To make things easier, we’ll use the natural logarithm of the likelihood function, ı , which is as follows:
ı i = 1 m l o g [ g j ( X i : m : n ) ] + R i l o g [ 1 G j ( X i : m : n ) ] ,
The maximum-likelihood estimates (MLEs) of the parameter vector Ω = ( a ^ 1 , b ^ 1 , c ^ 1 , s ^ 1 , r ^ 1 , a ^ 2 , b ^ 2 , c ^ 2 , s ^ 2 , r ^ 2 , p ^ ) are calculated by taking partial derivatives of (16) w.r.t. the parameters, and setting them equal to zero. These equations cannot be solved analytically, and we need to consider adopting any iterative techniques, such as simulated annealing, or Newton–Raphson type algorithm. In this case, we adopt the second choice for the iterative algorithm, i.e., the Newton–Raphson method.

Fisher Information Matrix (FIM)

The FIM is important in the calculation of uncertainty and other aspects of estimation for a wide range of statistical methods and applications, including parameter estimation, and experimental design for more details see [19].
The FIM is an excellent indicator of how much information sample data can provide regarding parameters. Assume f ( x ;   Ω ) is the density function and ı ( x _   | a j , b j , c j , s j , r j , p , q ) = l o g L ( x _   | a j , b j , c j , s j , r j , p , q ) is associated with the log-likelihood function. We can define the expected FIM, I, as follows:
I = E [ 2   ı Ω i Ω j ] | i , j = 1 , 2 , 3 , 4 , 5 ,
We may investigate the global maxima of the log-likelihood by setting different starting values for the parameters. The FIM will be required for interval estimation. The elements of 11 × 11 observed FIM (since expected values are different to calculate), J ( Ω ) = J ( Ω ) ^ , can be obtained from the authors upon request. The asymptotic distribution of [ ( Ω ) ^ Ω ] is N 11 ( Ω   ,   K ( Ω ) 1 ) , under the standard regularity conditions, where K ( Ω ) = E [ K ( Ω ) ] , is the expected information matrix, and J ( Ω ) ^ 1 is the observed information matrix. The multivariate normal N 11 ( Ω   ,   K ( Ω ) 1 ) distribution can be used to construct approximate confidence intervals for the individual parameters. The asymptotic variance-covariance matrix of the MLE Ω ^ = ( a ^ 1 , b ^ 1 , c ^ 1 , s ^ 1 , r ^ 1 , a ^ 2 , b ^ 2 , c ^ 2 , s ^ 2 , r ^ 2 , p ^ ) , can be obtained from the inverse of the observed FIM as: V 11 × 11 = K 1 ( Ω ^ ) = [ ν 11 ν 12 ν 1   11 ¯ ν 21 ν 22 ν 2   11 ¯ ν 11 ¯   1   ν 11 ¯   2 ν 11 ¯   11 ¯ ] 11 × 11 .
Then, based on the asymptotic normality of the MLE, a 100 ( 1 δ ) % approximate confidence interval for the parameters (say) a ^ 1 can be obtained as:
a ^ 1 ± Z 1 δ 2 v 11 ,

4. Bayesian Estimation

In recent years, Bayes’ paradigm has gained popularity in a range of fields, including engineering, clinical medicine, biology, and so on. Its ability to analyze earlier (prior) data makes it particularly useful in dependability studies, where data availability is one of the most significant challenges. This section develops the Bayes estimates and corresponding credible intervals of the model parameters, Ω = ( a 1 , b 1 , c 1 , s 1 , r 1 ,   a 2 , b 2 , c 2 , s 2 , r 2 , p ) ,   for   the   density   in   ( 6 ) .

4.1. Prior Information and Loss Function

As the gamma distribution can take on a variety of shapes depending on its parameter values, employing independent gamma priors is straightforward and can result in more expressive posterior density estimates. As a result, we consider gamma density priors, which are more flexible and convenient than other less informative independent prior distributions, in order to tailor support for the MEKGEKF distribution parameters. Therefore, the independent gamma priors for the MEKGEKF distribution parameters, Ω = ( a 1 , b 1 , c 1 , s 1 , r 1 ,   a 2 , b 2 , c 2 , s 2 , r 2 , p ) are assumed to be G a m m a ( α j , β j ) ; j = 1 , , 10 , respectively. A logical assumption for an appropriate prior for the mixing weight parameter p could be a uniform (0,1), which we have assumed in the context. The joint prior in this case will be:
π ( Ω ) j = 1 10 Ω j α j 1 e β j Ω j ,
where α j , β j ; j = 1 , , 10 , that reflect the prior knowledge of the unknown parameters Ω = ( a 1 , b 1 , c 1 , s 1 , r 1 ,   a 2 , b 2 , c 2 , s 2 , r 2 ) . It is assumed that α j   and   β j are known and non-negative. Regarding the use of such priors in this context, see [20,21] and the references cited therein.
Next, we consider an appropriate loss function. According to [22], the choice of the symmetric loss function (SLF) is a critical issue in Bayesian analysis. The squared error loss function (SEL) is the most commonly utilized SLF that is considered in this study for estimating the unknown parameters which is given by:
( Ω , Ω ˜ ) = ( Ω ˜ Ω ) 2 ,
where Ω ˜ is a close approximation of Ω . The objective is to use the above function to calculate the Bayesian estimates of the parameters to be obtained as posterior mean of Ω . On the other hand, any other loss functions, such as LINEX, composite, precautionary loss functions can be readily added as appropriate.

4.2. Posterior Analysis by SLF

Observing the progressively type II censored sample data from the likelihood function in (15), and combining with the prior knowledge as given earlier, yields the following form of the joint posterior density function. L ( x _   | Ω ) j = 1 10 Ω j α j 1 e β j Ω j i = 1 m g ( x i : m : n ; Ω ) [ 1 G ( x i : m : n ; Ω ) ] R i are the MEKGEKF density and the CDF given in (4) and (5), respectively.
The Bayes estimator of Ω (i.e., the parameter vector) will be the posterior expectation of Ω , denoted by Ω ˜ , under the SEL function. In order to obtain these estimators, the marginal posterior distributions for each of the parameters in Ω must be collected. However, explicit expressions for the marginal PDFs for each of the unknown parameters cannot be obtained simultaneously due to interactable and complicated mathematical computation. As a result, we compute Bayesian estimates and credible intervals using simulation methods such as MCMC techniques.
One of the most useful MCMC algorithms is the Metropolis–Hastings (MH) algorithm which is used to generate random samples using the posterior density distribution. Additionally, an independent proposal distribution to approximate Bayesian estimates is applied to create the associated Highest Posterior Density (HPD) credible intervals. Furthermore, this method provides a chain form of the Bayesian estimates that are easy to utilize in practice. For more information on this algorithm, see [23,24] and the references cited therein.

5. Monte Carlo Simulation

To compare the performance of the different estimators mentioned earlier, under both the classical and Bayesian paradigm, we build a Monte Carlo simulation of maximum likelihood estimates for MEKGEKF distribution based on a progressively type II samples obtained under different schemes at first.

5.1. Simulation Study

Several simulation studies were carried out to evaluate the performance of the MLE based on various censoring schemes. We offer a detailed simulation study that compares the performance of the likelihood estimation approach with Bayesian inference assuming gamma prior distributions for each parameter. In simulation studies, the sample size (n), censored progression size (m), replication (N), and different techniques are all changed in a systematic way.

5.2. Simulation Design

A censored sample for the MEKGEKF model in the simulation inquiry was created using a progressively type II censored sample. We define the scheme with replication, N = 10,000, as follows:
-
The total sample size (n) was altered, resulting in two levels of n = 100 and 200.
-
In the presence of m < n , and i = 1 m R i + m = n , the size of the progressive censored sample (m) was changed, generating two levels: m = 70, and 85, when n = 100, and m = 150 and 185, when n = 200.
-
The following two censored sample techniques were considered:
-
Scheme I: R i = 0 ; i = 1 , , m 1 , R m = n m .
-
Scheme II: R i = 0 ; i = 2 , , m , R 1 = n m .
-
We create two models, one with parameters ( a 1 , b 1 , c 1 , s 1 , r 1 ,   a 2 , b 2 , c 2 , s 2 , r 2 , p ) and the other with parameters a j = a , b j = b , c j = c ; j = 1 , 2 . The true values of the parameters for the first model are a 1 = 1.4 ,   b 1 = 1.5 ,   c 1 = 1.35 ,   r 1 = 1.7 ,   s 1 = 1.2 ,   a 2 = 1.5 ,   b 2 = 0.9 ,   c 2 = 0.5 ,   r 2 = 1.5 ,   s 2 = 1.3 and p = 0.3 and 0.7.
-
We determine the length of the confidence interval using a 95% confidence level.

5.3. Simulation Study

For the Monte Carlo simulation, the estimation methods indicated in Section 3 and Section 4 were employed to estimate the model parameters. To acquire the desired MLEs, the iterative NR approach is numerically implemented (as closed form expressions for the MLE are not available in this case) using the ‘maxLik’ package in R. The regularity conditions are satisfied for approximate normality assumption, asymptotic confidence intervals for each of the parameters are computed using the formula as given in Section 3. MCMC techniques and the MH algorithm were used to create Bayesian estimators based on the independent gamma priors as distributed earlier.

5.4. Comment on the Simulation Study

For each predicted model parameter, the bias, the mean square error (MSE), and the length of confidence intervals (L.CI) were calculated. Table 1 and Table 2 show the estimated values for the eight parameters of MEKGEKF model. The predicted results for the 11 parameters are shown in Table 3 and Table 4. There is some interesting information that can be observed from these tables. As the sample size n and m increases, the estimates become more accurate, implying that they are asymptotically unbiased which a desirable property. When we increase the value of parameter p , the mixing component to 1, the bias, MSE and L.CI decrease. Furthermore, the MSE decreases as the sample size increases in all situations, implying that these estimates are consistent. When comparing between the two estimates, we observe that the Bayes estimates have the lowest MSE in the vast majority of cases. The L.CI for estimates approaches 0 as it grows, indicating that the CI is the shortest. However, we cannot say that the Bayesian method will be uniformly better in all situations.

6. Real Data Applications

We consider several lifetime data sets in this section to demonstrate how well this new finite mixture distribution fits for illustrative purposes. For the components (of the mixture) of the distribution’s efficacy, we calculated the Akaikes information criterion (AIC), the Bayesian information criterion (BIC), the Hannan Quinn information criterion (HQIC), and the Kolmogorov–Smirnov (K-S) values. The parameters were estimated using the MLE method, and the MLE optimizations are done using the Nelder–Mead technique, which is a numerical approach for finding the global maximum of an objective function in a multidimensional space, and the R software is utilized.

6.1. Operation Data on Jobs Made of Iron Sheet

The data set consists of 50 observations (in millimeters), the hole diameter is 12 mm, and the sheet thickness is 3.15 mm, as reported in [25]. The data values are: 0.04, 0.02, 0.06, 0.12, 0.14, 0.08, 0.22, 0.12, 0.08, 0.26, 0.24, 0.04, 0.14, 0.16, 0.08, 0.26, 0.32, 0.28, 0.14, 0.16, 0.24, 0.22, 0.12, 0.18, 0.24, 0.32, 0.16, 0.14, 0.08, 0.16, 0.24, 0.16, 0.32, 0.18, 0.24, 0.22, 0.16, 0.12, 0.24, 0.06, 0.02, 0.18, 0.22, 0.14, 0.06, 0.04, 0.14, 0.26, 0.18, 0.16.
We conjecture that the data have interesting characteristics if we divide it into two parts and also conjecture that a mixing distribution (finite mixture) will be adequate to explain the hidden characteristics for the data. The two-component mixture of EKF and EKG distribution was applied to the data set given as.
Subpopulation I: 0.04, 0.06, 0.12, 0.22, 0.08, 0.26, 0.14, 0.08, 0.32, 0.14, 0.16, 0.12, 0.24, 0.16, 0.08, 0.16, 0.32, 0.24, 0.22, 0.24, 0.02, 0.22, 0.06, 0.14, 0.26; these data are applied to EKF distribution.
Subpopulation II: 0.02, 0.14, 0.08, 0.12, 0.24, 0.04, 0.16, 0.26, 0.28, 0.24, 0.22, 0.18, 0.32, 0.14, 0.24, 0.16, 0.18, 0.16, 0.12, 0.06, 0.18, 0.14, 0.04, 0.18, 0.16; these data are applied to EKG distribution.
From Table 5 and Table 6, we note that EKF is the best model for each data, but the p-value for EKG is larger than EKF for data set II. Therefore, the first distribution EKF is good for data set I, and the second distribution EKG is good for data set II in the mixture model. However, either of the distributions cannot provide a good fit for the entire data set.
Table 6 shows the different goodness-of-fit measures values as AIC, BIC, CAIC, and HQIC for EKG and EKF distribution for the hole diameter data. Here, we conclude that the EKF model is better than the EKG model.
Figure 2 and Figure 3 show the Estimated CDF and PDF for EKG and EKF distribution for Subpopulation I and estimated CDF and PDF for EKG and EKF distribution for Subpopulation II. While, the PP-plot for EKG and EKF distribution for Subpopulation I and the PP-plot for EKG and EGF distribution for Subpopulation II are indicated in Figure 4 and Figure 5, respectively.
Table 7 report the MLE and Bayesian estimation parameters of mixture of exponentiated Kumaraswamy Gompertz and exponentiated Kumaraswamy Fréchet distribution. From the reported results, we conclude that the Bayesian estimation is preforming better than the MLE where the standard error (SE) values are smaller compared the SE values obtained under the MLE method.
From the above summary measures, it appears that the MEKGEKF model might be a reasonably good fit for the data.

6.2. Wire Data

In the Wire Fatigue Experiment [26], a 48-stranded stainless-steel wire was ruptured by clamping it in needle-nose pliers and hanging a 1.65-pound weight on it while using 3/4 of a liter of water, then a 2.2-pound weight while using 1 liter of water. The pliers were spun clockwise and counterclockwise by 180 degrees. The number of half twists that resulted in total rupture (failure) was counted. For the Wire Fatigue Experiment, the wire data represent the number of half twists to total rupture as follows: 37, 30, 27, 51, 10, 24, 15, 14, 34, 34, 42, 25, 15, 13, 16, 12, 27, 21, 37, 35, 18, 17, 17, 13, 35, 27, 41, 41, 14, 17, 20, 16, 28, 24, 32, 24, 17, 19, 15, 20, 45, 39, 27, 33, 18, 13, 11, 13.
From Table 8, we note that EKF is the fitting model for Wire data, but the p-value of EKF is larger than EKG for Wire data. Figure 6 and Figure 7 shows that the shape of the probability density function is bimodal for both EKG and EKF distribution but the original data shape is uni-modal. Table 9 shows different goodness-of-fit measures values such as the AIC, BIC, CAIC, and the HQIC for EKG and EKF distribution for the hole diameter data.
Table 10 illustrate the MLE and the Bayesian estimates for the fitted MEKGEF model for the Wire data. Consequently, we conclude that the EKF is petter than EKG model. However, from the above summary, it can be said that component-wise, either of the EKG and the EKF might not adequately fit the data. Consequently, we conjecture that the 11-parameter MEKGEKF distribution in (6) will be a good fit and in the next, we fit this distribution to this data set.

6.3. Australian Athletes Data Set

These data were gathered as part of a study that looked at how data on various blood parameters differed according to the athlete’s sport body size and gender. There are 202 observations on 13 variables in this data set (for more details see [27]). The variables rcc (red blood cell count), wcc (white blood cell count), and bmi (body mass index) were investigated (body mass index).
The data values are 3.80 3.90 3.90 3.91 3.95 3.95 3.96 3.96 4.00 4.02 4.03 4.06 4.07 4.08 4.09 4.09 4.10 4.11 4.11 4.12 4.13 4.13 4.14 4.15 4.16 4.16 4.17 4.17 4.19 4.20 4.20 4.21 4.23 4.23 4.24 4.24 4.25 4.26 4.26 4.27 4.27 4.30 4.31 4.31 4.32 4.32 4.32 4.35 4.36 4.36 4.37 4.38 4.38 4.39 4.40 4.40 4.40 4.41 4.41 4.41 4.42 4.42 4.44 4.44 4.44 4.45 4.45 4.46 4.46 4.46 4.46 4.46 4.48 4.49 4.50 4.50 4.51 4.51 4.51 4.51 4.52 4.53 4.54 4.55 4.56 4.57 4.58 4.62 4.63 4.63 4.63 4.64 4.66 4.68 4.71 4.71 4.71 4.71 4.73 4.75 4.75 4.76 4.77 4.77 4.78 4.81 4.81 4.82 4.82 4.83 4.83 4.83 4.83 4.84 4.86 4.86 4.87 4.87 4.87 4.87 4.87 4.87 4.88 4.89 4.89 4.90 4.90 4.91 4.91 4.92 4.93 4.93 4.94 4.95 4.95 4.96 4.97 4.97 4.98 4.99 5.00 5.00 5.00 5.01 5.01 5.01 5.02 5.02 5.03 5.03 5.03 5.03 5.04 5.04 5.08 5.09 5.09 5.09 5.10 5.11 5.11 5.11 5.11 5.11 5.13 5.13 5.13 5.13 5.16 5.16 5.16 5.16 5.17 5.17 5.18 5.21 5.21 5.22 5.22 5.24 5.24 5.25 5.29 5.31 5.32 5.33 5.33 5.34 5.34 5.34 5.34 5.38 5.40 5.48 5.48 5.49 5.50 5.59 5.66 5.69 5.93 6.72.
From Figure 8 and Figure 9, it appears that, component-wise, EKG and EKF will not provide an adequate fit to the given data. The p-value in Table 11 also supports this assessment. As before, we conjecture that the 11 parameter MEKGEKF distribution might provide a good fit to the data. We fit the proposed distribution and the goodness-of-fit measures are reported in Table 12. The MLE and the Bayesian estimates for the fitted MEKGEF model for the Australian athletes data are shown in Table 13.
From the above summary measures, it appears that the proposed distribution given in (6) is a reasonable model to fit the above data.

7. Concluding Remarks

Classical and Bayesian inferences for finite mixture models in the case of absolutely continuous probability models as subpopulations is not new in the literature except for the fact that probability distribution(s) defined on the unit interval (0,1) has not been considered effectively earlier. In this paper, we discuss the utility of a finite mixture model for which the components are also some mixtures with Kumaraswamy distribution as one of the mixing components under the frequentist approach, the method of the maximum likelihood is adopted while for the Bayesian estimation, independent gamma priors are considered for all the model parameters of the derived model which we call the MEKGEKF distribution. The performance of both these estimation methods are assessed in the light of a progressively censored Type II random samples drawn from the newly developed probability model. From the simulation study (under various parameter settings and various censoring scheme), it appears that this MEKGEKF distribution might be useful in analyzing certain dataset(s) for which either or both of its component distributions will be inadequate to completely explain the data.

Author Contributions

All authors have contributed equally. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Princess Nourah bint Abdulrahman University Researchers Supporting Project number (PNURSP2022R50), Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data used to support the findings of this study are included within the article.

Acknowledgments

Princess Nourah bint Abdulrahman University Researchers Supporting Project number (PNURSP2022R50), Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia).

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Some representative PDF and hrf plots MEKGEKF distribution.
Figure 1. Some representative PDF and hrf plots MEKGEKF distribution.
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Figure 2. Estimated CDF and PDF for EKG and EKF distribution for Subpopulation I.
Figure 2. Estimated CDF and PDF for EKG and EKF distribution for Subpopulation I.
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Figure 3. Estimated CDF and PDF for EKG and EKF distribution for Subpopulation II.
Figure 3. Estimated CDF and PDF for EKG and EKF distribution for Subpopulation II.
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Figure 4. PP-plot for EKG and EKF distribution for Subpopulation I.
Figure 4. PP-plot for EKG and EKF distribution for Subpopulation I.
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Figure 5. PP-plot for EKG and EGF distribution for Subpopulation II.
Figure 5. PP-plot for EKG and EGF distribution for Subpopulation II.
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Figure 6. Estimated CDF and PDF for EKG and EKF distribution for Wire data.
Figure 6. Estimated CDF and PDF for EKG and EKF distribution for Wire data.
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Figure 7. PP-plot for EKG and EGF distribution for Wire data.
Figure 7. PP-plot for EKG and EGF distribution for Wire data.
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Figure 8. Estimated CDF and PDF for EKG and EKF distribution for Australian Athletes data.
Figure 8. Estimated CDF and PDF for EKG and EKF distribution for Australian Athletes data.
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Figure 9. PP-plot for EKG and EGF distribution for Australian Athletes data.
Figure 9. PP-plot for EKG and EGF distribution for Australian Athletes data.
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Table 1. MLE and the Bayesian estimates for eight parameters of MEKGEKF model based on a progressively Type II censoring scheme: scheme II.
Table 1. MLE and the Bayesian estimates for eight parameters of MEKGEKF model based on a progressively Type II censoring scheme: scheme II.
a = 1.5, b = 0.9, c = 0.5, r_1 = 1.7, s_1 = 1.2, r_2 = 1.5, s_2 = 1.3
P0.70.3
Scheme IIMLEBayesianMLEBayesian
nm BiasMSEL.CIBiasMSEL.CIBiasMSEL.CIBiasMSEL.CI
10070a1.45486.80078.49270.46681.96681.45921.82148.86699.24360.38831.88831.3945
b−0.07310.53182.8472−0.06360.44240.42540.08810.73463.3453−0.29260.60740.4434
c2.64428.24258.09011.01691.51691.12051.63715.70728.55440.88211.38210.9838
r10.46630.51382.13600.36680.36821.00430.69531.26133.46080.58071.02811.1577
s10.71982.34715.30680.19471.39470.91990.52442.98106.4548−0.07881.12120.9274
r20.18691.35674.51130.09801.15980.96340.37251.56404.68450.16641.26660.8129
s2−1.15141.33230.3210−0.82030.47970.4600−1.11851.25810.3265−0.84000.46000.3424
p0.07850.00900.20980.07710.00780.14570.20330.04430.21370.12070.04350.1531
85a1.07353.40357.92200.09611.59610.59300.75093.28216.23010.02481.52480.5898
b0.02980.47022.2867−0.31470.40590.34210.07390.37702.3438−0.21030.35690.4124
c2.16596.46447.19590.31580.81580.44901.01883.06385.28100.12330.62330.4289
r10.31160.40862.19010.22190.29220.55810.62641.17623.47400.12910.82910.5640
s10.17822.07485.0643−0.03301.16700.55810.15321.16074.1844−0.06941.10650.5794
r20.17211.05543.9483−0.08121.03760.57730.03540.66463.1958−0.11580.38420.4881
s2−0.99141.31580.3947−0.28910.40110.4262−1.11331.24840.3724−0.31240.39880.2603
p0.03270.00370.20260.02780.00270.13690.10120.01350.22510.09370.01140.1824
200150a1.28075.32177.52890.61642.11641.25001.39765.62777.90950.53932.03931.1342
b−0.08670.40372.4697−0.13290.38570.35690.07210.57463.3201−0.24980.50160.4257
c2.65556.54398.31651.29121.79120.92272.692912.18918.71891.14801.64800.8290
r10.43640.43181.92800.70400.40400.78170.57310.92783.03780.65580.83560.9415
s10.36952.01723.10010.29941.49940.76520.41592.40435.8615−0.00861.19140.8643
r20.12840.91313.71560.20820.70820.82650.19561.04533.93760.19200.96920.7567
s2−1.14281.31460.3652−0.92090.37910.2273−1.12681.27570.3018−0.92250.37750.1827
p0.06180.00570.16820.06900.00540.09830.16830.03020.16950.17350.03050.1063
185a0.37121.17915.80750.12860.96290.54821.03365.46246.21480.04751.54750.6107
b0.06360.37082.2926−0.13270.35730.24550.06340.43402.3366−0.19770.45700.3614
c1.12423.03134.82620.42490.92490.44521.81145.85206.29130.19930.69930.4343
r10.25210.31061.95010.35040.30500.46810.55070.85732.92060.20790.79080.5322
s10.32831.72363.58730.02321.22320.49980.16311.43174.6513−0.00711.08230.5209
r20.11840.79063.3970−0.11380.32860.52880.01250.62783.1087−0.09120.57410.4166
s2−1.10511.30320.3158−0.48500.28150.2048−1.09261.20350.3852−0.45550.32840.1485
p0.01010.00220.18170.01500.00200.09120.04700.00430.17800.05200.00350.0913
Table 2. MLE and the Bayesian estimates for eight parameters of MEKGEKF model based on a progressively type II censoring scheme: scheme I.
Table 2. MLE and the Bayesian estimates for eight parameters of MEKGEKF model based on a progressively type II censoring scheme: scheme I.
a = 1.5, b = 0.9, c = 0.5, r_1 = 1.7, s_1 = 1.2, r_2 = 1.5, s_2 = 1.3
P0.30.7
Scheme IMLEBayesianMLEBayesian
nm BiasMSEL.CIBiasMSEL.CIBiasMSEL.CIBiasMSEL.CI
10070a1.48126.31497.96560.19601.69601.25240.76043.53886.75170.32841.82841.2715
b−0.15080.47062.6259−0.13140.45860.4919−0.47300.34181.3479−0.44530.33450.5120
c1.57213.83984.59030.53461.03460.97661.07493.45954.07810.83901.33900.9246
r10.68331.04922.99460.44620.94621.08260.63801.11633.30450.56131.00261.2121
s10.75312.47205.41560.08471.28471.01121.20793.38595.44690.26831.46831.0754
r20.13920.66783.1597−0.09200.54080.72150.18131.98995.4894−0.13131.36871.1678
s2−1.09211.20240.3869−0.72000.58000.5644−1.16201.40990.9592−0.80080.49920.6737
p0.00100.00580.29800.00110.00430.19280.12290.03660.57470.11460.02810.3735
85a1.17484.00356.56850.00371.50370.62300.51373.17545.73230.07621.57620.5899
b0.06810.46302.1043−0.12910.40710.4652−0.30680.33501.2984−0.30510.25490.4072
c1.46293.08984.27040.05720.55720.41621.00833.28523.00890.28260.78260.4511
r10.60970.90172.85640.10980.80980.56430.26230.40832.28630.19400.38940.6012
s10.45662.15145.4069−0.05491.14510.57050.43892.11874.7618−0.02431.17570.5946
r20.09050.64093.1212−0.09170.53340.47490.08330.63794.9202−0.12730.53270.5981
s2−1.08271.18160.3772−0.25090.50490.5743−0.91671.03740.4335−0.27830.40220.6075
p−0.00090.00280.20850.00110.00190.18610.00230.00190.36350.02200.00170.2700
200150a1.38295.15007.23630.33541.83541.15770.99952.91885.76860.47161.97161.1515
b−0.01770.46832.6845−0.30240.45980.4052−0.43100.33471.2514−0.41110.30490.4348
c1.36783.27934.37450.80151.30150.83671.96783.40244.26801.07991.57990.9326
r10.44270.58082.43420.56140.42610.91970.51180.74592.72990.56230.63231.3790
s10.55531.91724.97710.14691.34690.87261.41193.27175.14760.36301.56301.0576
r2−0.00660.52902.8538−0.02020.47980.60390.38411.62865.0738−0.02331.47671.0847
s2−1.10671.12340.3784−0.85660.44340.3079−1.17441.34080.6693−0.93000.37000.3243
p−0.00280.00240.19200.00750.00230.12900.08810.02460.50850.08530.01790.3166
185a1.09344.65956.32120.02871.52870.60730.83022.50914.24230.11041.61040.5314
b0.02250.40134.0693−0.20020.37000.3351−0.14520.29521.2400−0.33790.24560.2406
c1.17332.61554.09810.14410.64410.40891.06932.62012.96310.40320.90320.4197
r10.40780.47172.37430.18920.38890.50340.27040.26881.73610.34180.20420.4676
s10.28061.32234.3758−0.06971.13030.52381.03711.71794.02850.04321.24320.5002
r20.00200.50822.6992−0.02910.43710.39730.09050.60673.1853−0.01720.43280.4848
s2−0.85090.90020.3291−0.41110.38890.4614−1.15930.93490.2850−0.46710.28330.2518
p−0.00240.00210.17820.00400.00190.1234−0.01370.00130.1905−0.00620.00170.1343
Table 3. MLE and the Bayesian estimates for 11 parameters of MEKGEKF model based on a progressively type II censoring scheme: scheme II.
Table 3. MLE and the Bayesian estimates for 11 parameters of MEKGEKF model based on a progressively type II censoring scheme: scheme II.
a1 = 1.4, b1 = 1.5, c1 = 1.35, r1 = 1.7, s1 = 1.2, a2 = 1.5, b2 = 0.9, c2 = 0.5, r2 = 1.5, s2 = 1.3
P0.30.7
Scheme IIMLEBayesianMLEBayesian
nm BiasMSEL.CIBiasMSEL.CIBiasMSEL.CIBiasMSEL.CI
10070a10.44851.33834.18430.81741.21741.25100.90933.88094.39640.93902.33901.2002
b1−1.10701.27220.8496−0.51500.98500.5027−1.27961.52341.0292−0.52340.97660.5162
c11.33673.99925.83670.62821.97820.90961.23552.94454.67261.05082.40081.1619
r11.67723.37342.93770.59532.29531.05901.49942.58922.29160.77602.47600.8898
s10.60090.98593.1016−0.28720.91280.61800.87921.49612.5483−0.18381.01620.6048
a2−0.24850.61202.91090.27370.57741.0895−0.49130.87732.86240.02420.75241.3380
b20.65861.38433.8256−0.12640.77360.87450.16400.71823.30030.11010.60101.0924
c20.39090.47462.22590.43650.36500.67010.42690.43201.95410.08240.35820.7868
r2−0.24690.16251.2503−0.03590.14640.3180−0.20240.36991.9086−0.03220.30470.8715
s2−0.11250.37772.3709−0.82560.34740.5580−0.15850.43442.5441−0.31620.39841.0596
p0.19880.04330.24010.19940.04100.18090.08160.00870.17840.07770.00780.1363
85a10.30651.07303.88260.23031.00630.56930.81412.42054.20240.32391.72390.5744
b1−1.01401.23390.7704−0.35190.91480.4980−1.09481.23600.7595−0.46370.80360.4194
c10.89851.78663.88310.18371.53370.53311.18302.25453.62840.30171.65170.5316
r11.59913.06122.81450.13441.83440.55421.42352.34582.21740.23641.93640.5461
s10.56370.86872.6718−0.23130.79690.55530.84501.35842.0761−0.16240.96160.4623
a2−0.24940.60582.8028−0.01660.48340.5798−0.38860.80922.3781−0.03590.74640.6107
b20.57451.37583.55450.04470.69450.51350.14010.42582.50090.02750.39280.5811
c20.31870.29861.7418−0.01940.24810.36580.30400.36371.0437−0.08260.24170.3953
r2−0.20910.15301.0279−0.04330.14570.3050−0.02070.19401.7265−0.04990.14500.5383
s20.00570.37102.3901−0.30310.29970.5172−0.14400.40472.2562−0.10940.21910.5856
p0.09520.01210.21470.09150.01310.17210.03550.00350.16840.02980.00270.1270
200150a10.94702.28724.62710.91282.12771.30010.41141.10613.79810.95551.03551.1540
b1−1.07141.19840.8828−0.82150.67850.4174−1.12401.30730.8212−0.59840.90160.4386
c11.19532.50504.07091.02432.37431.08031.02622.12784.06770.82281.17280.9477
r11.41832.28672.05850.94112.06410.77551.62811.98232.62460.79621.49620.9049
s10.83921.20032.76340.22451.02420.83030.63190.90072.7787−0.18070.70190.6244
a2−0.42190.77723.0374−0.00400.60501.2278−0.31760.65212.91350.29090.47911.0640
b20.12700.51652.77570.13880.40390.95060.55990.84572.86270.04410.44120.5725
c20.29760.39112.15840.09450.25950.76210.40420.40921.94570.41930.39190.6277
r2−0.10370.16791.5555−0.10610.13940.6315−0.27690.14211.0037−0.06190.11440.3238
s2−0.12330.40922.4630−0.28840.35011.0169−0.09640.35172.2962−0.71220.25880.3846
p0.06400.00540.14140.06490.00480.11310.17160.03080.14370.17480.03050.1083
185a10.69991.79764.48710.40911.28090.57140.31990.87133.44100.30340.70340.5722
b1−0.90981.02410.7362−0.59810.59020.3495−1.13331.32080.7489−0.45070.49330.4471
c11.02932.16563.89150.39311.74310.48480.93301.92064.02110.27921.06290.4622
r11.32271.96781.83360.36601.20660.45310.70031.31642.55920.23410.93410.5152
s10.81911.07312.6907−0.16270.95040.44530.57120.80092.7834−0.23300.69670.4539
a2−0.35380.72523.0395−0.00350.46450.5451−0.15510.55912.8702−0.01690.48310.5817
b20.12170.45382.74940.05260.29530.49580.48730.06541.70680.08270.05980.4627
c20.28320.27991.7535−0.08770.24120.35250.27620.25981.6809−0.02670.20470.3522
r2−0.09740.14751.4579−0.06730.12430.4490−0.23400.12580.8074−0.06820.11430.2717
s2−0.12230.35282.1519−0.10730.31930.5755−0.00680.33012.2542−0.27240.23030.2507
p0.01580.00170.14510.01680.00140.10180.04640.00350.14350.05200.00310.1015
Table 4. MLE and the Bayesian estimates for 11 parameters of MEKGEKF model based on a progressively type II censoring. scheme: scheme I.
Table 4. MLE and the Bayesian estimates for 11 parameters of MEKGEKF model based on a progressively type II censoring. scheme: scheme I.
a1 = 1.4, b1 = 1.5, c1 = 1.35, r1 = 1.7, s1 = 1.2, a2 = 1.5, b2 = 0.9, c2 = 0.5, r2 = 1.5, s2 = 1.3
P0.30.7
Scheme IMLEBayesianMLEBayesian
nm BiasMSEL.CIBiasMSEL.CIBiasMSEL.CIBiasMSEL.CI
10070a10.51690.90053.12270.58180.81821.31060.92910.80083.79940.65310.53151.2357
b1−1.08681.32100.6667−0.43081.06920.5615−1.07631.19350.7364−0.63170.86830.6844
c10.96211.55943.12380.46561.48160.98161.08941.28963.30350.58481.09350.9631
r11.58412.91462.49820.47812.17811.14601.18021.94162.90640.45021.15021.2367
s10.74780.99382.5870−0.22920.97080.68860.61270.63431.9965−0.26320.53680.8088
a2−0.30180.53852.62470.21640.47161.1929−0.36510.51803.21540.01580.45161.2552
b2−0.19020.64582.3351−0.41750.48250.6701−0.20090.56332.8375−0.13740.47631.1678
c20.38150.17651.41980.46040.16040.6813−0.09640.12201.31720.09200.11590.7786
r2−0.38970.13871.1633−0.07280.12720.41860.14800.35812.2753−0.04500.34550.6009
s2−0.08000.31662.1854−0.92770.29370.4913−0.38430.30371.7090−1.02970.27030.3944
p−0.00470.00280.20600.00830.00220.19570.14300.00240.53120.12340.00180.3952
85a10.46480.89023.05210.18690.75870.56950.85790.79023.23670.31120.47110.5680
b1−1.01031.32500.6171−0.29381.01620.4734−1.08780.92110.6491−0.46540.34550.4141
c10.86101.47133.03530.15111.35010.54211.12630.93233.34930.27940.62940.5311
r11.06152.80122.49890.13161.83160.57001.14111.68502.42810.21930.95920.5909
s10.70700.93602.5915−0.19750.90020.52490.60320.60551.7194−0.25200.45950.4923
a2−0.27240.50732.5823−0.00700.41930.5672−0.30980.47683.0619−0.01500.40850.5739
b20.71370.60782.1882−0.01770.45880.5102−0.26740.46202.4521−0.02070.38790.6074
c20.23790.17221.3590−0.02160.14780.39030.09150.12061.2677−0.04080.10460.4210
r2−0.29220.12940.9379−0.06870.11430.36040.02480.12991.8790−0.04430.10460.4184
s2−0.02700.30312.1257−0.31220.28990.4602−0.25040.23721.6183−0.29820.20020.2621
p−0.00430.00210.17980.00800.00130.17510.02450.00110.34080.01570.00110.2787
200150a10.49240.82092.98430.81630.72161.16660.40700.81442.06890.39240.63241.1376
b1−1.10251.24180.6369−0.51720.98280.4745−1.08671.21040.6747−0.70200.79800.5389
c10.90061.33962.85240.68581.03580.91911.18912.44673.98740.83282.18280.9474
r11.49272.51052.08480.69262.39260.93990.99811.51572.82790.68861.38861.2945
s10.76470.98642.4866−0.17651.02350.59300.79261.03172.4925−0.12621.00740.7845
a2−0.18300.44112.50520.23840.37381.0668−0.34520.62292.78490.08980.58981.1480
b20.08440.33462.2454−0.23430.26660.4900−0.14910.51432.7525−0.17350.47261.1703
c20.16300.17541.51380.43050.12930.6352−0.02140.18481.68480.21580.17160.7023
r2−0.28890.13280.8715−0.05810.14420.32930.12600.25771.9296−0.03640.24640.5144
s2−0.07630.29262.1012−0.76790.25320.4059−0.37090.38221.9407−0.90830.35920.4977
p−0.00370.00150.15090.00440.00130.12730.11780.02860.47540.11030.01810.3326
185a10.32110.81982.32200.28760.68760.57720.38510.42112.01110.34220.38220.5432
b1−0.91231.22900.6076−0.41460.85360.4177−1.06021.16310.5776−0.54550.69550.3386
c10.85631.30472.36350.24711.05970.54391.02881.56993.74590.39771.37480.5035
r10.95882.38231.91530.21551.91550.53650.82681.27941.69050.36651.06650.4808
s10.67540.39582.2693−0.22230.29780.44400.59790.94262.2685−0.11790.90210.4345
a2−0.16670.40772.2629−0.01000.34900.5817−0.32270.58032.2811−0.02380.47620.5296
b20.06910.31532.22460.03160.21930.4818−0.11250.45672.6146−0.00050.39000.5644
c20.15970.17561.4510−0.02700.11470.35240.02350.13131.2992−0.03810.12460.3373
r2−0.23540.13060.7670−0.08490.12420.2977−0.08720.15621.5124−0.02600.14400.3774
s20.02590.28302.0265−0.27290.27090.3511−0.17010.24211.8152−0.25020.14980.4551
p−0.00180.00130.13870.00370.00110.1257−0.00720.00180.1644−0.00430.00170.1477
Table 5. MLE, stander error (SE), KS test, and p-value for different sets for the hole data.
Table 5. MLE, stander error (SE), KS test, and p-value for different sets for the hole data.
Set abcrsKSp-Value
IEKGestimates11.03005.419714.05392.32182.55870.15150.6142
SE11.00440.03180.31921.53410.0018
EKFestimates0.16422836.50020.18660.5723250.15620.17030.4634
SE0.00300.11820.03820.00240.0027
IIEKFestimates3.1161232708.1500.24340.38129.61460.16920.4716
SE0.01667.84290.05850.00810.0163
EKGestimates8.71291.88487.82613.85064.82800.12480.8309
SE7.91661.17590.91062.46143.1271
Table 6. Goodness-of-fit measures, AIC, BIC, CAIC, and HQIC for the hole diameter data.
Table 6. Goodness-of-fit measures, AIC, BIC, CAIC, and HQIC for the hole diameter data.
AICCAICBICHQIC
IEKF−45.4153−42.2575−39.3210−43.7250
EKG−42.6578−39.4999−36.5634−40.9674
IIEKF−48.6074−45.4495−42.5130−46.9170
EKG−47.9072−44.7493−41.8128−46.2168
Table 7. MLE and the Bayesian estimates for the fitted MEKGEKF model.
Table 7. MLE and the Bayesian estimates for the fitted MEKGEKF model.
MLEBayesian
EstimatesSELowerUpperEstimatesSELowerUpper
a18.777463.085643.540115.63588.274570.658077.158249.32375
b11.886481.2846004.30903.061300.577482.061834.26348
c17.849700,3756911.661211.66126.885410.428556.086977.70303
r13.780190.910450736361.45.143650.964333.610366.73922
s14.815771.409533.45847.02743.945900.573623.001865.08593
a20.198470.0054002.97250.898400.356950.178601.53123
b23120.22971.06436415.4816415.5022836.45480.274652835.9792836.886
c20.209240.037740139.47910.746960.525160.00301.5735
r20.543470.004090.46780.61570.340970.070580.211090.48834
s2250.31613.95647271.0581271.0741207.9667324.56475169.3517249.5836
P0.499730.0500108.25470.502110.229170.069050.87604
Table 8. MLE with standard error (SE) and KS test for different sets and different model for Wire data.
Table 8. MLE with standard error (SE) and KS test for different sets and different model for Wire data.
abcrsKSp-Value
EKGestimates37.231610.556633.45430.00840.01700.13910.3108
SE12.07422.905017.27270.00010.0011
EKFestimates23.15798.50000.11361.877612.71050.09710.7557
SE0.00280.00850.01640.00280.0028
Table 9. AIC, BIC, CAIC, and HQIC for different sets and different model for Wire data.
Table 9. AIC, BIC, CAIC, and HQIC for different sets and different model for Wire data.
AICCAICBICHQIC
EKG367.803369.2316377.159371.3387
EKF358.612360.0406367.968362.1476
Table 10. MLE and the Bayesian estimates for the fitted MEKGEF model for the Wire data.
Table 10. MLE and the Bayesian estimates for the fitted MEKGEF model for the Wire data.
MLEBayesian
EstimatesLowerUpperSEEstimatesLowerUpperSE
a137.16773.678570.656917.086336.868736.498436.91290.1100
b110.73004.111817.34823.376610.254210.121710.86380.2328
c135.962724.442447.48295.877734.512934.308034.97990.4061
r10.00840.00790.00890.00030.02810.02640.03070.0002
s10.01700.01480.01930.00120.16950.14910.19230.0017
a223.158423.153023.16380.002723.568023.541223.59670.0019
b29.49989.48299.51670.00869.17819.08409.36530.0082
c20.11520.08260.14780.01660.13500.07960.19230.0066
r21.87591.87051.88130.00272.45202.29822.63480.0015
s212.713312.707912.71860.00271.43241.40001.44880.0019
p0.50010.40010.60010.05100.08280.01020.14670.0388
Table 11. MLE with standard error (SE) and KS test for different sets and different model for Australian athletes data set.
Table 11. MLE with standard error (SE) and KS test for different sets and different model for Australian athletes data set.
abcrsKSp-Value
EKGestimates26.879123.148825.12630.19380.13000.07910.1595
SE10.67905.654616.52220.03700.0149
EKFestimates1.91746.20480.17957.87635.37660.08400.1152
SE0.91543.78070.36861.14370.4242
Table 12. AIC, BIC, CAIC, and HQIC for different sets and different model for Australian athletes data set.
Table 12. AIC, BIC, CAIC, and HQIC for different sets and different model for Australian athletes data set.
AICCAICBICHQIC
EKG263.2465263.5526279.7878269.9391
EKF257.1600257.4661273.7014263.8527
Table 13. MLE and the Bayesian estimates for the fitted MEKGEF model for the Australian athletes data.
Table 13. MLE and the Bayesian estimates for the fitted MEKGEF model for the Australian athletes data.
MLEBayesian
EstimatesLowerUpperSEEstimatesLowerUpperSE
a127.033919.222034.84583.985727.405827.014527.52920.1287
b120.816116.588425.04372.157020.473920.267720.62720.1151
c149.071037.473860.66835.917049.048848.912849.21900.0939
r10.17100.06880.27320.05210.24070.16010.33140.0500
s10.13850.09160.18550.02400.14720.11960.19130.0188
a22.04551.96972.12120.03862.55142.50242.58200.0158
b26.40456.23466.57440.08676.02285.99226.09300.0711
c20.16830.13950.19710.01470.47130.43270.51610.0108
r27.93887.87518.00250.03257.19167.03167.29290.0315
s25.36125.30215.42040.03020.31030.01810.52020.0298
p0.50020.45150.54900.02490.32120.31680.54860.0194
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Alotaibi, R.; Almetwally, E.M.; Ghosh, I.; Rezk, H. Classical and Bayesian Inference on Finite Mixture of Exponentiated Kumaraswamy Gompertz and Exponentiated Kumaraswamy Fréchet Distributions under Progressive Type II Censoring with Applications. Mathematics 2022, 10, 1496. https://doi.org/10.3390/math10091496

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Alotaibi R, Almetwally EM, Ghosh I, Rezk H. Classical and Bayesian Inference on Finite Mixture of Exponentiated Kumaraswamy Gompertz and Exponentiated Kumaraswamy Fréchet Distributions under Progressive Type II Censoring with Applications. Mathematics. 2022; 10(9):1496. https://doi.org/10.3390/math10091496

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Alotaibi, Refah, Ehab M. Almetwally, Indranil Ghosh, and Hoda Rezk. 2022. "Classical and Bayesian Inference on Finite Mixture of Exponentiated Kumaraswamy Gompertz and Exponentiated Kumaraswamy Fréchet Distributions under Progressive Type II Censoring with Applications" Mathematics 10, no. 9: 1496. https://doi.org/10.3390/math10091496

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