similar to: braking a label in two lines when using expression()

I making an xyplot and the y label is too long and needs to be in two rows, but when I brake it there is a huge gap between the last text string and the expression, and I can't get rid of it. Any ideas? Data: structure(list(Temp = c(8L, 8L, 8L, 8L, 8L, 8L, 12L, 12L, 12L, 12L, 12L, 12L), CO2 = c(380L, 380L, 380L, 750L, 750L, 750L, 380L, 380L, 380L, 750L, 750L, 750L), Treat = structure(c(3L,

Hi I have the following barchart to which I want to add error bars. library(lattice) barchart(Change~fTreat,groups=Process,change, auto.key=list(points=FALSE,rectangles=TRUE), panel=function(x, y,...){ panel.barchart(x,y,origin = 0,...); panel.abline(h=0,col="black",...); } ) I have tried

Dear All I am attempting some power analyses, based on simulated data. My experimental set up is thus: Bleach: main effect, three levels (control, med, high), Fixed. Temp: main effect, two levels (cold, hot), Fixed. Main effect interactions, six levels (fixed) For each main-effect combination I have three replicates. Within each replicate I can take varying numbers of measurements (response

Hi All, Another quick question - I noticed that COZIGAM has been removed from CRAN, and that you are referred to the archive for previous versions (last updated 23 July 2012). Is this package still ok to use? Or is there an alternative which might also fit zero-inflated GAMs? Thanks, Raeanne The Scottish Association for Marine Science (SAMS) is registered in Scotland as a Company Limited by

Hi there, My question is about the 'theta' parameter in specification of a NB GAMM. I have fit a GAM with an optimum structure of: SB.gam4<-gam(count~offset(vol_offset)+ s(Depth_m, by=StnF, bs="cs")+StageF*RegionF, family=negbin(1, link=log), data=Zoop_2011[Zoop_2011$SpeciesF=='SB',]) However, this GAM shows heterogeneity in the

Hi there, I'm using the lattice package to create an xy plot of abundance vs. depth for 5 stages of barnacle larvae from 5 species. Each panel of the plot represents a different stage, while different loess smoothers within each panel should represent different species. However, I would like depth to be on the y-axis and abundance to be on the x-axis, because this is more intuitive as an

Greetings everyone, I am running MDS on a very large dataset (12 x 25071 - 12 model runs with 25071 output values each), and also on a very much reduced version of the dataset (randomly select 1000 of the 25071 output values). I would like to look at similarities/dissimilarities between the 12 model runs. When I use metaMDS on the full dataset, I get a warning message: Warning message: In

Hi, I am fairly new to R and still trying to figure out how it all works, and I have run into a few issues. I apologize in advance if my questions are a bit basic, I'm also no statistics wizard, so part of my problem my be a more fundamental lack of knowledge in the field. I have a dataset that looks something like this: Week Subj Group Readout 0 1 A 352.2 1 1 A

Dear R Wizards, After much frustration and days of confusion I have finally broken down and am asking for help, which I don’t like doing, but I just can’t figure this one out on my own. I’ve conducted a laboratory experiment testing the effects of temperature and salinity on whether or not a biological event will occur (Go or NoGo). I’ve coded the factors temperature and salinity as factors for

Hi, I posted the message below last week, but no answers, so I'm giving it another attempt in case somebody who would be able to help might have missed it and it has now dropped off the end of the list of mails. I am fairly new to R and still trying to figure out how it all works, and I have run into a few issues. I apologize in advance if my questions are a bit basic, I'm also no

Good day all We have a voicetronix openline4 card.Asterisk is configured for sip with all the extensions and all&all. I can call out and internally,to dial out I have to dial 0... My problem is with incoming calls If I call my external PSTN number,asterisk answers with the default message and if I press the extension it goes to the right sip client. BUT As soon as I hangup this call all gets

Hi List, I'm following on the discussions regarding the use of exploratory factor analysis with binary data, from nabble: http://www.nabble.com/PCA--for-Binary-data-to11050371.html#a11092127 and i tried using FactorMineR package but unfortunately i have trouble understanding what are the types of the variables which AFDM is suitable for? I guessed from that example in ?AFDM that

Hi all, This is my first optimization code and am receiving the following error for the following function: fn <- function(p) { +263*log(sqrt(2*pi)*sd(test$A))+ sum(log(abs(c(test$A[-1], 1))^p[3])) + (sum(((test$A-p[1]+(p[2]+1)*c(test$A[-1], 1)))^2)/sum(sd(test$A)*(abs(c(test$A[-1], 1))^p[3])^2))/2 } out <- optim(fn, p = c(0.1, 0.1, 2.5), method="BFGS", hessian=TRUE) Error

Estimada Beatriz Entonces hay buenas noticias. Ese es un error muy común, es como que no aprendemos y siempre cometemos el mismo error, las veces que me paso a mi. Al respecto yo aprendí a realizar str(mis.datos) para ver ... Sobre la actualización, yo sufrí de un software que requería R pero en una versión “obsoleta”, entonces comencé a tener más de una versión de R instalada en mi computadora

Beatriz, Prueba legend("topleft",0,substitute(chi)). En mi PC funciona! En cuanto a LATEX, tienes razón, excede el tema de este foro, con lo que me reservo (lamentablemente) mis sugerencias. Saludos, Jose -----Original Message----- From: r-help-es-bounces en r-project.org [mailto:r-help-es-bounces en r-project.org] On Behalf Of Beatriz Lacruz Sent: 20 November 2009 15:13 To: Jorge Ivan

Hi Hadley: Not sure if you received my email, so I am resending it again. I have dealt with this before and I can't remember how it got resolved. It is too much data to reproduce the example below(49.000 records) but all I am after is trying to get the x axis breaks. I want my x axis to go from 27 to 51 and 1 to 25 by 2. I am trying to concatenate the breaks but it sorts the seq() in ascending

Dear Colleagues   I have the following code that generates a boxplot for one specific labtest:   boxplot.n(LBSTRESN~COHORT, main="Boxplot of laboratory data for XLXXX-XXX test=Creatinine", subset = LBTEST=="Creatinine", xlab = "Cohort Number", ylab = "Units = umol/L", varwidth=TRUE   I would like to know if there is a way to loop through the dataset and

I am running the sm.density.compare function amd I am getting the following error:   my code is  > sm.density.compare(LBSTRESN,COHORT,xlab="Units = umol/L"subset = LBTEST=="Creatinine")   Error in if (from == to) rep.int(from, length.out) else as.vector(c(from,  :   missing value where TRUE/FALSE needed   I do not understand the error and I have had no help when searching

Dear friends. I wanted to reproduce a sheet of paper useful for plotting the reciprocal of some biochemical variable (creatinine) over time (Bleyer Am J Kidney Dis 34:576-578,1999). Time on X axis with units years and months. On Y axis, 1/creatinine, but with the original creatinine value indicated - to make it easier for people to use it. When using the graph, the linear decrease in 1/crea over

el material lo podéis descargar de aquí http://goo.gl/PT30FB El 29 de octubre de 2013 15:59, Carlos Ortega <cof@qualityexcellence.es>escribió: > Hola Beatriz, > > Si me pasas el *.md lo subo a un Dropbox y si no es muy grande lo subo a > R-Hispano (linkándolo a la agenda).... > > Saludos, > Carlos. > > > El 29 de octubre de 2013 15:56, Gregorio R. Serrano