This vignette
provides a quick demo of the truh
package. The example that we consider here is taken from Figure 3 of the paper: Trambak Banerjee, Bhaswar B. Bhattacharya, Gourab Mukherjee Ann. Appl. Stat. 14(4): 1777-1805 (December 2020) <DOI: 10.1214/20-AOAS1362>.
We will consider a nonparametric two sample testing problem where the d dimensional baseline (or uninfected) sample \boldsymbol{U}=(U_1,\ldots,U_n) are i.i.d with cdf F_0 and the d dimensional treated (infected) sample \boldsymbol{V}=V_1,\ldots,V_m are i.i.d with cdf G. Here, we assume that the heterogeneity in the baseline population is reflected by K different subgroups, each having unimodal distributions with distinct modes and cdfs F_1,\ldots,F_K, and mixing proportions w_1,\ldots,w_K such that F_0=\sum_{a=1}^{K}w_aF_a~\text{where}~w_a\in(0,1)~\text{and}~\sum_{a=1}^{K}w_a=1.
The goal is to test the following composite hypothesis: H_0:G\in\mathcal{F}(F_0)~\text{versus}~H_1:G\notin\mathcal{F}(F_0), where \mathcal{F}(F_0) is the convex hull of F_1,\ldots,F_K. We take d=2,n=2000,m=500 and sample U_1,\ldots,U_n from F_0 where F_0=0.3N(\boldsymbol{0},\boldsymbol{I}_2)+0.3N(\boldsymbol{\mu}_1,\boldsymbol{I}_2)+0.4N(\boldsymbol{\mu}_2,\boldsymbol{I}_2), with \boldsymbol{\mu}_1=(0,-4) and \boldsymbol{\mu}_2=(4,-2).
= 2000
n = 2
d
#Sampling the baseline (uninfected)
set.seed(1)
<-runif(n,0,1)
pset.seed(10)
<- (p<=0.3)*matrix(rnorm(d*n),n,d)+
U>0.3 & p<=0.6)*cbind(matrix(rnorm(n),n,1),
(pmatrix(rnorm(n,-4),n,1))+
>0.6)*cbind(matrix(rnorm(n,4),n,1),
(pmatrix(rnorm(n,-2),n,1))
To sample V_1,\ldots,V_m we consider three settings for G.
# Sampling the treated (infected)
= 500
m set.seed(50)
<-cbind(matrix(rnorm(m,4),m,1),
V1matrix(rnorm(m,-2),m,1))
#Scatter plot of the data
= c(rep('Baseline',n),
grp rep('Treated',m))
plot(c(U[,1],V1[,1]), c(U[,2],V1[,2]),
pch = 19,
col = factor(grp),
xlab = 'X_1',
ylab = 'X_2')
# Legend
legend("topright",
legend = levels(factor(grp)),
pch = 19,
col = factor(levels(factor(grp))))
# Sampling the treated (infected)
= 500
m set.seed(20)
<-runif(m,0,1)
qset.seed(50)
<-(q<=0.5)*cbind(matrix(rnorm(m,2),m,1),
V2matrix(rnorm(m,-2),m,1))+
>0.5)*cbind(matrix(rnorm(m,3),m,1),
(qmatrix(rnorm(m,3),m,1))
#Scatter plot of the data
plot(c(U[,1],V2[,1]), c(U[,2],V2[,2]),
pch = 19,
col = factor(grp),
xlab = 'X_1',
ylab = 'X_2')
# Legend
legend("topright",
legend = levels(factor(grp)),
pch = 19,
col = factor(levels(factor(grp))))
# Sampling the treated (infected)
= 500
m set.seed(20)
<-runif(m,0,1)
qset.seed(50)
<-(q<=0.8)*matrix(rnorm(d*m),m,d)+
V3>0.8 & q<=0.9)*cbind(matrix(rnorm(m),m,1),
(qmatrix(rnorm(m,-4),m,1))+
>0.9)*cbind(matrix(rnorm(m,4),m,1),
(qmatrix(rnorm(m,-2),m,1))
#Scatter plot of the data
plot(c(U[,1],V3[,1]), c(U[,2],V3[,2]),
pch = 19,
col = factor(grp),
xlab = 'X_1',
ylab = 'X_2')
# Legend
legend("topright",
legend = levels(factor(grp)),
pch = 19,
col = factor(levels(factor(grp))))
Let us now execute the truh
testing procedure for these scenarios. Recall that the goal is to test the following composite hypothesis: H_0:G\in\mathcal{F}(F_0)~\text{versus}~H_1:G\notin\mathcal{F}(F_0).
- Setting 1: Here we know that G=F_0 and so H_0 is true.
library(truh)
.1 = truh(V1,U,B=200)
truh.1$pval truh
## [1] 0.375
So, truh
fails to reject the null hypothesis.
library(truh)
.2 = truh(V2,U,B=200)
truh.2$pval truh
## [1] 0
We see that truh
rejects the null hypothesis.
library(truh)
.3 = truh(V3,U,B=200)
truh.3$pval truh
## [1] 0.205
In this case, truh
makes the correct decision and fails to reject H_0.