similar to: 2 way repeated measures ANOVA using R: syntax and reporting question

Dear Gideon Unless you are willing to accept uncorrelated measures in time and homogeneity of variance I would go for a linear mixed model instead. You might be surprised on how diffrent can be your results. Try; >?lme I hope that this helps Francisco >From: GIDEON WASSERBERG <wasserberg at wisc.edu> >To: "R-help at lists.R-project.org" <R-help at

Hello, Darik Horn sent a pull request adding support for LZ4. LZ4 is supposed to be a very fast compression algorithm, especially when it comes to decompression. I did a quick benchmark with zlib, LZO and LZ4. Now, there are many benchmarks you can find online, but most of them deal with compressing large files. Tinc on the other hand has to compress small packets individually. So I did the

Hi, I am encountering a problem in reading a file, the file looks like that: T 3 0 -- -- -- T -- -- -- 18.98 3 1 6.75 4.39 39 -- -- -- 18.58 3 2 6.90 4.90 43 -- -- -- 18.63 3 3 7.07 5.39 48 -- -- -- 18.78 G 4 0 7.41 5.54 47 G

I've enabled the GSS code in dovecot, but our Kerberos nerds are complaining that it doesn't work :) I probably have the thing totally misconfigured (so don't worry about that part for now), but I do have a crash: Info: imap-login: Disconnected: rip=XXX.YYY.229.8, lip= XXX.YYY.17.59, TLS handshake Error: auth(default): gssapi(?,XXX.YYY.229.8): While acquiring service credentials: No

Hi! I want to choose part of the data. But it has a question. > attach(PIKO) > PIKO[1:5,] code species dbh x y tag status branch 92 10142 PIKO 38.9 6.05 12.81 10165 alive 0 109 10213 PIKO 41.0 6.71 26.21 10202 alive 0 135 10222 PIKO 48.3 18.98 21.28 10214 alive 0 146 10223 PIKO 47.0 19.45 22.83 10224 alive 0 147 10223 PIKO 20.0 19.74

R Help - I'm trying to run a correlation matrix with a covariate of "age" and will at some point will also want to covary other variables concurrently. I'm using the "psych" package and have tried other methods such as writing a loop to extract semi-partial correlations, but it does not seem to be working. How can I accomplish this? library(psych) > set.cor(y =

Hi, I wonder if anyone can help me with specifying a right model for my analysis. I am a beginner to lme methods and though have spent already many hours studying from various books an on-line helps, I was unfortunately not able to find a solution to my problem on my own. Data structure: I studied escape behavior of three species of a prey to a predator. The prey specimens (many) were in a

I am designing an interlaboratory validation study for a presence/absence alternative method test kit vs. a presence/absence reference method test kit. There will be 10 laboratories conducting tests using both methods. In each laboratory, there will be 5 specimens tested, each of the 5 specimens twice by both methods (alternative, standard). The total number of data are 10 x 5 x 4 = 200.

[Corrected the model formula to include "method".] I am designing an interlaboratory validation study for a presence/absence alternative method test kit vs. a presence/absence reference method test kit. There will be 10 laboratories conducting tests using both methods. In each laboratory, there will be 5 specimens tested, each of the 5 specimens twice by both methods (alternative,

Dear Sir or Madam? I am a doctor of urology,and I am engaged in developing a nomogram of bladder cancer. May I ask for your help on below issue? I set up a dataset which include 317 cases. I got the Binary Logistic Regression model by SPSS.And then I try to reconstruct the model ?lrm(RECU~Complication+T.Num+T.Grade+Year+TS)? by R-Project,and try to internal validate the model through

To anyone who can help: I have two brief questions concerning sapply. Following below is the code for my example. The two problems are described at the end of the code: site <- rep(2:6, each = 12) tillage <- rep(c(1,-1), each = 6, times = 5) carbon <- c(18.23, 16.06, 17.81, 16.07, 17.26, 17.08, 14.92, 15.88, 12.11, 14.23, 16.99, 13.57, 20.34, 20.3,

Hi all, i have a dataset of 3D coordinates and can't figure out how to' tell R which One Are the individuals: I have 3 columns which i named x,y and z And then i have 2607 Lines, but each specimen is 33 Lines (79 specimens) How can i tell R to' categorize individuals every 33 Lines? Thanks in advance

I'm trying to create maps of reptile abundance in different states & counties using data from Herp.net, which provides lists of specimens with the places that they were found. First I would like to parse the list by state using 2-letter abbreviations, since I'm focusing on certain regions. To do this, I've been trying to create a vector (state2) that gives all state names as

*Thanks* all those who took the time to help me (even if the "question" was not related to - the use of - R). Now I think I can soundly make my point w/ the referee (can I use your replies? If so I intend to properly cite its use?!?). Regards, Eduardo Esteves ps - Sorry for not explaining the "biological details" of my posting: RNA/DNA is the ratio of RNA content to

Hi..   R Program is shown ARIMA output as below then SARIMA equation is be   (1 - 0.991B^{12})z_t + 43.557 = (1+0.37B)(1-0,915B^{12})a_t    But I try to calculate it by manual . It look like it 's big different from R sofeware,   I am not sure this equation is correct or not . PLS supoort me to confirm it   Arima Model ( 0,0,1)(1,0,1)   No Transformation Constant   >> 43.557 , t = 10.09

On the source system: $ rsync --version rsync version 2.6.8 protocol version 29 Copyright (C) 1996-2006 by Andrew Tridgell, Wayne Davison, and others. <http://rsync.samba.org/> Capabilities: 64-bit files, socketpairs, hard links, ACLs, symlinks, batchfiles, inplace, IPv6, file flags, 32-bit system inums, 64-bit internal inums ... $ ll -d fcst-200[89] fcst-201[01] dr-xr-xr-x

Dear List, I am trying to?plot?bathymetry contours around the Hawaiian Islands using the package rgdal and PBSmapping.? I have run into a memory limit when trying to combine two fairly small objects using cbind().? I have increased the memory to 4GB, but am being told I can't allocate a vector of size 240 Kb.? I am running R 2.11.1 on a Dell Optiplex 760 with Windows XP.? I have pasted

Hi, what dovecot version is this? This looks a lot like bug that was fixed in 2.2.25.5 Sami > On 21 Jan 2020, at 17.59, Asai <asai at globalchangemusic.org> wrote: > > Greetings, > > Can anyone help me to solve this problem? > > When doveadm sync is running nightly, we have a certain user's mailbox that will not properly sync and the logs give me this error

Dear list, I'm trying to learn how to use nlme to be able to fit ad analyse mixed-model logistic regressions. In order to keep things simple, I started by the simplest possible model : a one (fixed-effect ...) continuous variable. This problem is, of course, solved by glm, but I wanted to look at a "hand-made" nls fit, in order to be able to "generalize" to nlme

Duncan, With r182593, the dragonegg 3.3 branch now completely passes the Polyhedron 2005 benchmarks using the FSF gcc 4.8.1svn compiler. Thanks. Jack Tested on x86_apple-darwin12 Compile Flags: -ffast-math -funroll-loops -O3 de-gfortran47: /sw/lib/gcc4.7/bin/gfortran -fplugin=/sw/lib/gcc4.7/lib/dragonegg.so -specs=/sw/lib/gcc4.7/lib/integrated-as.specs de-gfortran48: