similar to: maintaining specified factor contrasts when subsetting in lmer

On 09/29/2017 09:30 PM, rick sanchez wrote: > I am trying to get up geo replication between two gluster volumes > > I have set up two replica 2 arbiter 1 volumes with 9 bricks > > [root at gfs1 ~]# gluster volume info > Volume Name: gfsvol > Type: Distributed-Replicate > Volume ID: c2fb4365-480b-4d37-8c7d-c3046bca7306 > Status: Started > Snapshot Count: 0 > Number

On Thu, 25 Aug 2011 20:01:11 +1000 Silvia Pfeiffer <silvia at silvia-pfeiffer.de> wrote: > Hi BCXA, > > CMML is deprecated. You should use KATE instead. > > Cheers, > Silvia. ok i admit this statement came as a surprise for me. cmml is about metadate/annotations, how can it be replaced by KATE ( which is mainly about subtitles as far as i can see? startx

On Fri, 26 Aug 2011 18:08:59 +1000 Silvia Pfeiffer <silvia at silvia-pfeiffer.de> wrote: > On Fri, Aug 26, 2011 at 5:33 PM, startx <startx at plentyfact.org> wrote: > > On Thu, 25 Aug 2011 20:01:11 +1000 > > Silvia Pfeiffer <silvia at silvia-pfeiffer.de> wrote: > > > >> Hi BCXA, > >> > >> CMML is deprecated. You should use KATE

I am trying to get up geo replication between two gluster volumes I have set up two replica 2 arbiter 1 volumes with 9 bricks [root at gfs1 ~]# gluster volume info Volume Name: gfsvol Type: Distributed-Replicate Volume ID: c2fb4365-480b-4d37-8c7d-c3046bca7306 Status: Started Snapshot Count: 0 Number of Bricks: 3 x (2 + 1) = 9 Transport-type: tcp Bricks: Brick1: gfs2:/gfs/brick1/gv0 Brick2:

All, The code below is for a pseudo dataset of repeated measures on patients where there is also a treatment factor called "drug". Time is treated as categorical. What code is necessary to test for a treatment effect at a single time point, e.g., time = 3? Does the answer matter if the design is a crossover design, i.e, each patient received drug and placebo? Finally, what would

Hi David: In looking at your original post it is a bit difficult to ascertain exactly what your null hypothesis was. That is, you want to assess whether there is a treatment effect at time 3, but compared to what. I think your second post clears this up. You should refer to pages 224- 225 of Pinhiero and Bates for your answer. This shows how to specify contrasts. > -----Original Message-----

Dear list members, I am new to R and to the R-help list. I am trying to perform a mixed-model analysis using the lmer() function. I have a problem with the output anova table when using the anova() function on the lmer output object: I only get the numerator d.f., the sum of squares and the mean squares, but not the denominator d.f., F statistics and P values. Below is a sample output, following

Dear R help list, I have done a lot of searching but have not been able to find an answer to my problem. I apologize in advance if this has been asked before. I am applying a mixed model to my data using lmer. I will use sample data to illustrate my question: >library(lme4) >library(arm) >data("HR", package = "SASmixed") > str(HR) 'data.frame': 120 obs.

On Wed, Jan 24, 2018 at 11:49:13PM +0100, Luca 'remix_tj' Lorenzetto wrote: > Hello, > > i've started my migrations from vmware today. I had successfully > migrated over 200 VM from vmware to another cluster based on 4.0 using > our home-made scripts interacting with the API's. All the migrated vms > are running RHEL 6 or 7, with no SELinux. > > We