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...od on the win2k machine, or at least hear about some diagnostic tools I can use. I'm a programmer, but I always had a sysadmin to handle network stuff for me. New to linux on PC's, but not to unix in general. So I'm ignorant, but capable. smb.conf: [global] workgroup = LINDBLOOM-AIREY server string = Samba Server hosts allow = 192.168.1. 127. printcap name = /etc/printcap load printers = yes log file = /var/log/samba/%m.log max log size = 50 security = user password level = 8 username level = 8 encrypt passwords = yes smb passwd file = /etc/samba/smbpass...

Dear List, I downloaded R for the first time yesterday, in the hopes that I might deal more effectively with a complex repeated measures experimental design involving inbred strains of laboratory mice. The design below, somewhat simplified, cannot be computed with standard ANOVA, because something called the X'X matrix is too large. The design has the following factors: Between-subject

We need a two-way non-parametric ANOVA in order to analysis properly some ecological data, do you know any reference in R? or how to do it? Thank you very much All the best diana -- View this message in context: http://www.nabble.com/Two-way-non-parametric-ANOVA--tp15039308p15039308.html Sent from the R help mailing list archive at Nabble.com.

Hello. I am posting this on behalf of a student in my class. I have been introducing them to R. I suspect that the problem I need help with is not so much an R issue, but a MAC config issue, but I don't have enough MAC experience to know what to do. Anyway, on to the problem. We are using Frank Harrell's Hmisc and Design packages. This student also wishes to use the latex formatting

Hi all, I will be teaching a graduate-level course on R at CU Boulder next semester. I have a teaching idea that might also help improve the R wiki page... I wanted to know what you all thought of it and wanted to solicit some advice about doing it. During the latter part of the course, students will choose a topic of interest (e.g., hierarchical linear modeling), and show how to achieve it in

To estimate saturation binding parameters Bmax and Kd in a receptor saturation binding experiment, I use the following nonlinear equation and the nls() function: bmax*X*dummy ------------ + ns*X + background = total binding kd+X where X is concentration, and dummy is an indicator to allow shared estimation of the nonspecific binding parameter ns. This equation describes two fitted

When a variance components mixed model is run in Stata, if some of the variance components are zero, the model may not converge, for rational reasons. However, when the same model is run in SAS, the models with variance components that estimate to zero nonetheless converge. If I'm interested in looping through a set of such models, the SAS behavior is preferred. However, in Stata

Dear list, Has anyone created a version of SSmicmen that allows testing for group differences? The basic Michaelis-Menten equation is: (Bmax * X) / (Kd + X). The nlme package allows modeling of random effects for Bmax and Kd as needed, but I curious how I can build in group differences? I have receptor binding data for strains of mice, and following Pinheiro and Bates' lead in their