Free Statistics

of Irreproducible Research!

Author's title

Author*The author of this computation has been verified*
R Software Modulerwasp_One Factor ANOVA.wasp
Title produced by softwareOne-Way-Between-Groups ANOVA- Free Statistics Software (Calculator)
Date of computationTue, 02 Nov 2010 16:57:34 +0000
Cite this page as followsStatistical Computations at FreeStatistics.org, Office for Research Development and Education, URL https://freestatistics.org/blog/index.php?v=date/2010/Nov/02/t1288716975bl91z3sjs2wglh6.htm/, Retrieved Sun, 28 Apr 2024 01:14:08 +0000
Statistical Computations at FreeStatistics.org, Office for Research Development and Education, URL https://freestatistics.org/blog/index.php?pk=91858, Retrieved Sun, 28 Apr 2024 01:14:08 +0000
QR Codes:

Original text written by user:
IsPrivate?No (this computation is public)
User-defined keywords
Estimated Impact138
Family? (F = Feedback message, R = changed R code, M = changed R Module, P = changed Parameters, D = changed Data)
-     [One-Way-Between-Groups ANOVA- Free Statistics Software (Calculator)] [Golfballs] [2010-10-25 12:27:51] [b98453cac15ba1066b407e146608df68]
F   PD  [One-Way-Between-Groups ANOVA- Free Statistics Software (Calculator)] [WS5 Q6.1 KT] [2010-10-28 19:53:10] [afe9379cca749d06b3d6872e02cc47ed]
F R P       [One-Way-Between-Groups ANOVA- Free Statistics Software (Calculator)] [WS 5 Q 6] [2010-11-02 16:57:34] [7131fefee4115a2a717140ef0bdd6369] [Current]
Feedback Forum
2010-11-07 17:38:09 [50992571857ef0dcfd2a4644b51ec6d0] [reply
De student veranderde de intercept van true naar false en gebruikte ook te weinig data. Hierdoor had de student ook de foute response variable en factor variable en verkreeg de student foutieve informatie. Als we naar de voorbeeldoplossing kijken zien we dat Treatment ‘E’ duidelijk de beste treatment op korte termijn is. Dit komen we te weten door naar de laatste kolom (p adj) te kijken.


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Dataseries X:
0	'T'
0	'T'
1	'T'
0	'T'
0	'T'
0	'T'
0	'T'
1	'T'
1	'T'
0	'T'
0	'T'
1	'T'
1	'T'
1	'T'
0	'T'
0	'T'
0	'T'
0	'T'
1	'T'
0	'T'
0	'T'
0	'T'
0	'T'
-1	'T'
0	'T'
-1	'T'
0	'T'
0	'T'
0	'T'
0	'T'
-1	'T'
0	'T'
0	'T'
0	'T'
0	'T'
0	'T'
0	'T'
1	'E'
1	'E'
0	'E'
0	'E'
0	'E'
0	'E'
0	'E'
0	'E'
1	'E'
1	'E'
0	'E'
0	'E'
0	'E'
1	'E'
0	'E'
1	'E'
0	'E'
1	'E'
1	'E'
1	'E'
1	'E'
0	'E'
0	'E'
1	'E'
0	'E'
0	'E'
-1	'E'
0	'E'
1	'E'
1	'E'
0	'E'
0	'E'
0	'E'
1	'S'
1	'S'
1	'S'
1	'S'
0	'S'
-1	'S'
0	'S'
0	'S'
-1	'S'
0	'S'
0	'S'
0	'S'
0	'S'
-1	'S'
0	'S'
0	'S'
-1	'S'
0	'S'
0	'S'
0	'S'
0	'S'
0	'S'
0	'S'
1	'S'
0	'S'
0	'S'
0	'S'
0	'S'
0	'S'
0	'S'
0	'S'
0	'S'
0	'S'
0	'S'
1	'S'




Summary of computational transaction
Raw Inputview raw input (R code)
Raw Outputview raw output of R engine
Computing time2 seconds
R Server'RServer@AstonUniversity' @ vre.aston.ac.uk

\begin{tabular}{lllllllll}
\hline
Summary of computational transaction \tabularnewline
Raw Input & view raw input (R code)  \tabularnewline
Raw Output & view raw output of R engine  \tabularnewline
Computing time & 2 seconds \tabularnewline
R Server & 'RServer@AstonUniversity' @ vre.aston.ac.uk \tabularnewline
\hline
\end{tabular}
%Source: https://freestatistics.org/blog/index.php?pk=91858&T=0

[TABLE]
[ROW][C]Summary of computational transaction[/C][/ROW]
[ROW][C]Raw Input[/C][C]view raw input (R code) [/C][/ROW]
[ROW][C]Raw Output[/C][C]view raw output of R engine [/C][/ROW]
[ROW][C]Computing time[/C][C]2 seconds[/C][/ROW]
[ROW][C]R Server[/C][C]'RServer@AstonUniversity' @ vre.aston.ac.uk[/C][/ROW]
[/TABLE]
Source: https://freestatistics.org/blog/index.php?pk=91858&T=0

Globally Unique Identifier (entire table): ba.freestatistics.org/blog/index.php?pk=91858&T=0

As an alternative you can also use a QR Code:  

The GUIDs for individual cells are displayed in the table below:

Summary of computational transaction
Raw Inputview raw input (R code)
Raw Outputview raw output of R engine
Computing time2 seconds
R Server'RServer@AstonUniversity' @ vre.aston.ac.uk







ANOVA Model
A ~ B
means0.3640.0570.108

\begin{tabular}{lllllllll}
\hline
ANOVA Model \tabularnewline
A  ~  B \tabularnewline
means & 0.364 & 0.057 & 0.108 \tabularnewline
\hline
\end{tabular}
%Source: https://freestatistics.org/blog/index.php?pk=91858&T=1

[TABLE]
[ROW][C]ANOVA Model[/C][/ROW]
[ROW][C]A  ~  B[/C][/ROW]
[ROW][C]means[/C][C]0.364[/C][C]0.057[/C][C]0.108[/C][/ROW]
[/TABLE]
Source: https://freestatistics.org/blog/index.php?pk=91858&T=1

Globally Unique Identifier (entire table): ba.freestatistics.org/blog/index.php?pk=91858&T=1

As an alternative you can also use a QR Code:  

The GUIDs for individual cells are displayed in the table below:

ANOVA Model
A ~ B
means0.3640.0570.108







ANOVA Statistics
DfSum SqMean SqF valuePr(>F)
B34.911.6375.7390.001
Residuals10229.090.285

\begin{tabular}{lllllllll}
\hline
ANOVA Statistics \tabularnewline
  & Df & Sum Sq & Mean Sq & F value & Pr(>F) \tabularnewline
B & 3 & 4.91 & 1.637 & 5.739 & 0.001 \tabularnewline
Residuals & 102 & 29.09 & 0.285 &   &   \tabularnewline
\hline
\end{tabular}
%Source: https://freestatistics.org/blog/index.php?pk=91858&T=2

[TABLE]
[ROW][C]ANOVA Statistics[/C][/ROW]
[ROW][C] [/C][C]Df[/C][C]Sum Sq[/C][C]Mean Sq[/C][C]F value[/C][C]Pr(>F)[/C][/ROW]
[ROW][C]B[/C][C]3[/C][C]4.91[/C][C]1.637[/C][C]5.739[/C][C]0.001[/C][/ROW]
[ROW][C]Residuals[/C][C]102[/C][C]29.09[/C][C]0.285[/C][C] [/C][C] [/C][/ROW]
[/TABLE]
Source: https://freestatistics.org/blog/index.php?pk=91858&T=2

Globally Unique Identifier (entire table): ba.freestatistics.org/blog/index.php?pk=91858&T=2

As an alternative you can also use a QR Code:  

The GUIDs for individual cells are displayed in the table below:

ANOVA Statistics
DfSum SqMean SqF valuePr(>F)
B34.911.6375.7390.001
Residuals10229.090.285







Must Include Intercept to use Tukey Test

\begin{tabular}{lllllllll}
\hline
Must Include Intercept to use Tukey Test  \tabularnewline
\hline
\end{tabular}
%Source: https://freestatistics.org/blog/index.php?pk=91858&T=3

[TABLE]
[ROW][C]Must Include Intercept to use Tukey Test [/C][/ROW]
[/TABLE]
Source: https://freestatistics.org/blog/index.php?pk=91858&T=3

Globally Unique Identifier (entire table): ba.freestatistics.org/blog/index.php?pk=91858&T=3

As an alternative you can also use a QR Code:  

The GUIDs for individual cells are displayed in the table below:

Must Include Intercept to use Tukey Test







Levenes Test for Homogeneity of Variance
DfF valuePr(>F)
Group21.110.334
102

\begin{tabular}{lllllllll}
\hline
Levenes Test for Homogeneity of Variance \tabularnewline
  & Df & F value & Pr(>F) \tabularnewline
Group & 2 & 1.11 & 0.334 \tabularnewline
  & 102 &   &   \tabularnewline
\hline
\end{tabular}
%Source: https://freestatistics.org/blog/index.php?pk=91858&T=4

[TABLE]
[ROW][C]Levenes Test for Homogeneity of Variance[/C][/ROW]
[ROW][C] [/C][C]Df[/C][C]F value[/C][C]Pr(>F)[/C][/ROW]
[ROW][C]Group[/C][C]2[/C][C]1.11[/C][C]0.334[/C][/ROW]
[ROW][C] [/C][C]102[/C][C] [/C][C] [/C][/ROW]
[/TABLE]
Source: https://freestatistics.org/blog/index.php?pk=91858&T=4

Globally Unique Identifier (entire table): ba.freestatistics.org/blog/index.php?pk=91858&T=4

As an alternative you can also use a QR Code:  

The GUIDs for individual cells are displayed in the table below:

Levenes Test for Homogeneity of Variance
DfF valuePr(>F)
Group21.110.334
102



Parameters (Session):
par1 = 1 ; par2 = 2 ; par3 = FALSE ;
Parameters (R input):
par1 = 1 ; par2 = 2 ; par3 = FALSE ;
R code (references can be found in the software module):
cat1 <- as.numeric(par1) #
cat2<- as.numeric(par2) #
intercept<-as.logical(par3)
x <- t(x)
x1<-as.numeric(x[,cat1])
f1<-as.character(x[,cat2])
xdf<-data.frame(x1,f1)
(V1<-dimnames(y)[[1]][cat1])
(V2<-dimnames(y)[[1]][cat2])
names(xdf)<-c('Response', 'Treatment')
if(intercept == FALSE) (lmxdf<-lm(Response ~ Treatment - 1, data = xdf) ) else (lmxdf<-lm(Response ~ Treatment, data = xdf) )
(aov.xdf<-aov(lmxdf) )
(anova.xdf<-anova(lmxdf) )
load(file='createtable')
a<-table.start()
a<-table.row.start(a)
a<-table.element(a,'ANOVA Model', length(lmxdf$coefficients)+1,TRUE)
a<-table.row.end(a)
a<-table.row.start(a)
a<-table.element(a, paste(V1, ' ~ ', V2), length(lmxdf$coefficients)+1,TRUE)
a<-table.row.end(a)
a<-table.row.start(a)
a<-table.element(a, 'means',,TRUE)
for(i in 1:length(lmxdf$coefficients)){
a<-table.element(a, round(lmxdf$coefficients[i], digits=3),,FALSE)
}
a<-table.row.end(a)
a<-table.end(a)
table.save(a,file='mytable.tab')
a<-table.start()
a<-table.row.start(a)
a<-table.element(a,'ANOVA Statistics', 5+1,TRUE)
a<-table.row.end(a)
a<-table.row.start(a)
a<-table.element(a, ' ',,TRUE)
a<-table.element(a, 'Df',,FALSE)
a<-table.element(a, 'Sum Sq',,FALSE)
a<-table.element(a, 'Mean Sq',,FALSE)
a<-table.element(a, 'F value',,FALSE)
a<-table.element(a, 'Pr(>F)',,FALSE)
a<-table.row.end(a)
a<-table.row.start(a)
a<-table.element(a, V2,,TRUE)
a<-table.element(a, anova.xdf$Df[1],,FALSE)
a<-table.element(a, round(anova.xdf$'Sum Sq'[1], digits=3),,FALSE)
a<-table.element(a, round(anova.xdf$'Mean Sq'[1], digits=3),,FALSE)
a<-table.element(a, round(anova.xdf$'F value'[1], digits=3),,FALSE)
a<-table.element(a, round(anova.xdf$'Pr(>F)'[1], digits=3),,FALSE)
a<-table.row.end(a)
a<-table.row.start(a)
a<-table.element(a, 'Residuals',,TRUE)
a<-table.element(a, anova.xdf$Df[2],,FALSE)
a<-table.element(a, round(anova.xdf$'Sum Sq'[2], digits=3),,FALSE)
a<-table.element(a, round(anova.xdf$'Mean Sq'[2], digits=3),,FALSE)
a<-table.element(a, ' ',,FALSE)
a<-table.element(a, ' ',,FALSE)
a<-table.row.end(a)
a<-table.end(a)
table.save(a,file='mytable1.tab')
bitmap(file='anovaplot.png')
boxplot(Response ~ Treatment, data=xdf, xlab=V2, ylab=V1)
dev.off()
if(intercept==TRUE){
thsd<-TukeyHSD(aov.xdf)
bitmap(file='TukeyHSDPlot.png')
plot(thsd)
dev.off()
}
if(intercept==TRUE){
a<-table.start()
a<-table.row.start(a)
a<-table.element(a,'Tukey Honest Significant Difference Comparisons', 5,TRUE)
a<-table.row.end(a)
a<-table.row.start(a)
a<-table.element(a, ' ', 1, TRUE)
for(i in 1:4){
a<-table.element(a,colnames(thsd[[1]])[i], 1, TRUE)
}
a<-table.row.end(a)
for(i in 1:length(rownames(thsd[[1]]))){
a<-table.row.start(a)
a<-table.element(a,rownames(thsd[[1]])[i], 1, TRUE)
for(j in 1:4){
a<-table.element(a,round(thsd[[1]][i,j], digits=3), 1, FALSE)
}
a<-table.row.end(a)
}
a<-table.end(a)
table.save(a,file='mytable2.tab')
}
if(intercept==FALSE){
a<-table.start()
a<-table.row.start(a)
a<-table.element(a,'TukeyHSD Message', 1,TRUE)
a<-table.row.end(a)
a<-table.start()
a<-table.row.start(a)
a<-table.element(a,'Must Include Intercept to use Tukey Test ', 1, FALSE)
a<-table.row.end(a)
a<-table.end(a)
table.save(a,file='mytable2.tab')
}
library(car)
lt.lmxdf<-levene.test(lmxdf)
a<-table.start()
a<-table.row.start(a)
a<-table.element(a,'Levenes Test for Homogeneity of Variance', 4,TRUE)
a<-table.row.end(a)
a<-table.row.start(a)
a<-table.element(a,' ', 1, TRUE)
for (i in 1:3){
a<-table.element(a,names(lt.lmxdf)[i], 1, FALSE)
}
a<-table.row.end(a)
a<-table.row.start(a)
a<-table.element(a,'Group', 1, TRUE)
for (i in 1:3){
a<-table.element(a,round(lt.lmxdf[[i]][1], digits=3), 1, FALSE)
}
a<-table.row.end(a)
a<-table.row.start(a)
a<-table.element(a,' ', 1, TRUE)
a<-table.element(a,lt.lmxdf[[1]][2], 1, FALSE)
a<-table.element(a,' ', 1, FALSE)
a<-table.element(a,' ', 1, FALSE)
a<-table.row.end(a)
a<-table.end(a)
table.save(a,file='mytable3.tab')