similar to: Split Plot and Tukey

Displaying 20 results from an estimated 300 matches similar to: "Split Plot and Tukey"

2010 Nov 03
1
Tukey's table
Hi, I'm building Tukey's table using qtukey function. It happens that I can't get the values of Tukey's one degree of freedom and also wanted to eliminate the first column. The program is: Trat <- c(1:30) # number of treatments gl <- c(1:30, 40, 60, 120) # degree freedom tukval <- matrix(0, nr=length(gl), nc=length(Trat)) for(i in
2011 Feb 16
1
Hartley's table
Hi, I used the commands below to make Hartley's table, but some values are NA. require(SuppDists) trat = seq(2, 15, 1) gl = seq(2, 40, 1) har = matrix(0, nr=length(gl), nc=length(trat)) for(i in 1:length(gl)) for(j in 1:length(trat)) har[i,j] <- qmaxFratio(.95, df=gl[i], k=trat[j]) rownames(har) <- gl colnames(har) <- trat head(har) The output (head): 2
2012 Feb 06
1
multiple comparisons in nested design
Dear professors and collegues I need to perform a analysis of dates from a nested experimental design. From "Bioestatical Analysis" of Zar "Bimetry of Sokal" & Rohlf "Design and Analysis of Experiments" of Montgomery I have: Sum (mean(x)_i - mean(x)_T)2 / (a-1) -> var(epsilon) + n sigma2_B + n b (sum alfa_i)2 / (a-1) Sum (mean(x)_ij - mean(x)_i)2 /
2008 Feb 23
1
Error in ma.svd(X, 0, 0) : 0 extent dimensions
Hi, I run a maanova analysis and found this message error: Error in ma.svd(X, 0, 0) : 0 extent dimensions I did a google search and found this: \item ma.svd: function to compute the sigular-value decomposition of a rectangular matrix by using LAPACK routines DEGSVD AND ZGESVD. \item fdr: function to calculate the adjusted P values for FDR control. I did a search for LAPACK and
2011 Aug 16
1
Fit Gompertz' curve'
Hi, I build a graph taking into account the times: 1, 2,4,6,8,10,12,15,18,21,24,28,32 and 48. Be that the scale of the X axis does not look right. It seems equidistant. (graph attached) What changes have I to do in the following commands so that the scale be correct? interaction.plot(Tempo, Trat, Valor, ylim=c(0, 2), las=1, lty=c(1,2,3,4), lwd=3, bty='l',
2003 Aug 14
1
gnls - Step halving....
Hi all, I'm working with a dataset from 10 treatments, each treatment with 30 subjects, each subject measured 5 times. The plot of the dataset suggests that a 3-parameter logistic could be a reasonable function to describe the data. When I try to fit the model using gnls I got the message 'Step halving factor reduced below minimum in NLS step'. I´m using as the initial values of the
2012 Apr 20
4
Problem with Tukey test
I'm new using R im trying to do a tukey test, but when i see the results the p value results in NA im guessing its because i have missing values but im not sure how to fix it AnovaModel.2 <- aov(area ~ trat, data=apilados) > summary(AnovaModel.2) Df Sum Sq Mean Sq F value Pr(>F) trat 4 11847 2961.76 9.9905 1.500e-06 *** Residuals 76 22531 296.46
2010 Aug 09
1
Different colour in each bar in lattice package
Hi, I try to plot bars with different colours in a barchart graphic. My idea is make that all X-Levels from trat var with different colour (grey scale). I search for a solution but dont find any. Any help? Thanks dados <- structure(list(Medias = c(0.994169096209855, 0.99416342412449, 0.974683544303797, 0.954430379746835, 0.669047619047619, 0.999999998475569, 0.994163424124514,
2010 Nov 29
4
subset
?Hi: I always use subset the same way but now is returning 0 rows. What's wrong with the way I am subsetting? library(ggplot2) structure(list(first = c(38.2086, 43.1768, 43.146, 41.8044, 42.4232, 46.3646, 38.0813, 40.0745, 40.4889, 38.6246, 40.2826, 41.6056, 34.5353, 40.0768), second = c(43.3295, 42.4326, 38.8994, 37.0894, 42.3218, 46.1726, 39.1206, 41.2072, 42.4874, 40.2657, 38.7766,
2010 Mar 14
1
Improve lattice XYPLOT graphic
Hi, How I could improve this graphic? http://www.divshare.com/download/10754700-f81 I would like to write groups labels in each panel and override the labels from object. I am try this code: xyplot(percentagem.mortos~tempo|trat, data=bio.ens, type="a", ? ? ? auto.key=list(points=FALSE, lines=TRUE, columns=3), ? ? ? ylim=c(0,100),scales = list(x = list(at = c(48, 72, 96), labels ? ?
2004 Jun 02
1
Manova and contrasts
Hi R-users I'm trying to do multivariate analysis of variance of a experiment with 3 treatments, 2 variables and 5 replicates. The procedure adopted in SAS is as follow, but I'm having difficulty in to implement the contrasts for comparison of all treatments in R. I have already read manuals and other materials about manova in R, but nothing about specific contrasts were found in them,
2005 Jun 13
1
Warning messages in lmer function (package lme4)
Hi: I'm using function lmer from package lme4, and I get this message: " There were 12 warnings (use warnings() to see them)" So I checked them: Warnings 1 to 11 said: 1: optim returned message ERROR: ABNORMAL_TERMINATION_IN_LNSRCH in: "LMEoptimize<-"(`*tmp*`, value = structure(list(maxIter = 50, ... and Warning 12 said: 12: IRLS iterations for glmm did
2023 Nov 21
1
Cambiar el intervalo de confianza en un anova
Buenas, En R, como en la mayoría del software estadístico, no se utiliza ningún nivel de confianza sino que lo que se calcula es el p-valor asociado al contraste. De forma que cuanto más cerca de 0 esté el p-valor "menos credibilidad le damos a la hipótesis nula". Dicho mejor, debemos rechazar la hipótesis nula si el p-valor está por debajo de nuestro nivel de confianza. Por ejemplo,
2002 May 02
2
plot survival points
Hi all, I have a little problem. I make an weibull survival analysis using the survival package. It,s OK, them I have the functions. I plot this funcions with curve(). I want to make a plot with the real survival points (proportion of alive x time) and them add the curves to points. I have the time to dead, the censor data and my trataments. To analysis the model is: model1 <-
2005 May 09
4
Error in F test on version 2.1.0
Hi, I make a upgrade to R 2.1.0 and in some analysis I give an error: anova(model,test="F") Analysis of Deviance Table Model: binomial, link: logit Response: landing/total Terms added sequentially (first to last) Df Deviance Resid. Df Resid. Dev F Pr(>F) NULL 16 105.079 trat 1 93.149 15 11.930 93.15 Warning message:
2023 Nov 21
1
Cambiar el intervalo de confianza en un anova
Gracias Carlos. Yo también he visto el ejemplo que te pone chatGPT, pero la salida que te da no soy capaz de interpretarla. Os paso las ordenes y las respuestas de R de la propuesta de chatGPT Ejemplo.aov<- aov(P~TRAT+CORTE+REP) > summary (Ejemplo.aov) Df Sum Sq Mean Sq F value Pr(>F) TRAT 6 0.0028 0.00046 0.777 0.590 CORTE 2 0.5022 0.25110 424.542 <2e-16
2013 Feb 28
2
Ayuda con función tapply
Hola Compañeros, Estoy tratando de "contar" utilizando la función tapply y length y obtengo un error que no entiendo. Agradecería su ayuda. Las líneas son las siguientes: UNO <- subset (datos, CRIH2008 == "VERDADERO") dim (UNO) Abund2008 <- tapply (UNO$Cons, list(UNO$Site, UNO$Trat), length, na.rm=T) Y obtengo este error: Error en FUN(X[[1L]], ...) : 2 arguments
2008 Aug 26
2
Do I need a special package to run LSD tests?
Hi there, I am trying to run LSD.test(model) I used the following commands: attach(model) m1<- glm(ttl.m ~ site+year, family=quasipoisson, data= model) df<-df.residual(m1) MSerror<-deviance(m1)/df The following command did not work: comparison<- LSD.test (ttl.m, site+year, df, MSerror, alpha = 0.05, group=FALSE) I get an error message: Error: could not find function
2009 Mar 27
3
color vectors other than gray()
I'm trying to create a graph where different cells of a grid (a shapefile) will be painted with a color share scale, where the most easy way is to use gray(). Can I somehow get a vector (gradient) of colors, a vector of colors with other methods but gray()? I'm doing this until now quad_N_sp <-
2007 Nov 13
0
Difficult to set a quiet formula in maanova
Hi, I am trying to run an analysis with the package maanova and I am not getting success. I suppose that I am wrong on set up the formula, so the issue may not be related to R, properly. I have two varieties of plants (V1 and V2). A group of each ones were treated and another was not treated. After treatment, in three different time RNA was collected from treated and from not treated plants for