similar to: ANOVA stuffs_How to save each result from FOR command?

Dear R experts, I'm beginner. My question about ANOVA for unequal sample sized data should be obsolete but I can not clarify it. I have a dataset from 23 males and 18 females. I measured one condition('cond') with 4 levels. So I'd like to see main effect of gender, cond and gender by cond interaction and also postHoc test. (In fact, I have to do anova 90 times) * 1. Question

DaeRyong Jeong reports a race between vhost_dev_cleanup() and vhost_process_iotlb_msg(): Thread interleaving: CPU0 (vhost_process_iotlb_msg) CPU1 (vhost_dev_cleanup) (In the case of both VHOST_IOTLB_UPDATE and VHOST_IOTLB_INVALIDATE) ===== ===== vhost_umem_clean(dev->iotlb); if (!dev->iotlb) { ret = -EFAULT; break; } dev->iotlb = NULL; The reason is

On Mon, May 21, 2018 at 10:38:10AM +0800, Jason Wang wrote: > > > On 2018?05?18? 17:24, Jason Wang wrote: > > > > > > On 2018?05?17? 21:45, DaeRyong Jeong wrote: > > > We report the crash: KASAN: use-after-free Read in vhost_chr_write_iter > > > > > > This crash has been found in v4.17-rc1 using RaceFuzzer (a modified > > >

On Mon, May 21, 2018 at 10:38:10AM +0800, Jason Wang wrote: > > > On 2018?05?18? 17:24, Jason Wang wrote: > > > > > > On 2018?05?17? 21:45, DaeRyong Jeong wrote: > > > We report the crash: KASAN: use-after-free Read in vhost_chr_write_iter > > > > > > This crash has been found in v4.17-rc1 using RaceFuzzer (a modified > > >

On 2018?05?17? 21:45, DaeRyong Jeong wrote: > We report the crash: KASAN: use-after-free Read in vhost_chr_write_iter > > This crash has been found in v4.17-rc1 using RaceFuzzer (a modified > version of Syzkaller), which we describe more at the end of this > report. Our analysis shows that the race occurs when invoking two > syscalls concurrently, write$vnet and

On 2018?05?17? 21:45, DaeRyong Jeong wrote: > We report the crash: KASAN: use-after-free Read in vhost_chr_write_iter > > This crash has been found in v4.17-rc1 using RaceFuzzer (a modified > version of Syzkaller), which we describe more at the end of this > report. Our analysis shows that the race occurs when invoking two > syscalls concurrently, write$vnet and

The ez package was developed to aid those that are new to statistical programming. Over the course of several years of helping colleagues and students learn R, I observed that folks are often initially turned off R because they have difficulty obtaining SPSS-like results quickly (SPSS is the dominant environment in my field, psychology). ez attempts to fill this gap, providing quick and easy

The ez package was developed to aid those that are new to statistical programming. Over the course of several years of helping colleagues and students learn R, I observed that folks are often initially turned off R because they have difficulty obtaining SPSS-like results quickly (SPSS is the dominant environment in my field, psychology). ez attempts to fill this gap, providing quick and easy

Hi, I have encountered this error when attempting a One-way Repeated-measure ANOVA with my data. I have read the "Anova in car: SSPE apparently deficient rank" thread by I'm not sure the within-subject interaction has more degrees of freedom than subjects in my case. I have prepared the following testing script: rm(list = ls())

Hi. Is it possible to make gpr from raw? library(aroma) #read gpr file gpr <- GenePixData$read("gpr123.gpr", path=aroma$dataPath) # gpr -> raw raw <- as.RawData(gpr) # raw -> ma ma <- getSignal(raw, bgSubtract=FALSE) ma.norm <- clone(ma) #normalization normalizeWithinSlide(ma.norm, "s") #ma -> raw raw2 <- as.RawData(ma) I want to make gpr data from

I had downloaded the program that runs on MS-DOS. Is it possible for MS-DOS to be run in R such as WinBugs1.4? I wonder whether there is the R function for running MS-DOS from R such as the 'bug.r' function to make Winbugs practicable in R. I had heard Rterm.exe that runs on MS-DOS. However, What I need is to run MS-DOS in R but to run R in MS-DOS.

I initially posted this question to one of the StackExchange sites, and they suggested that I repost my problem here. After using ezANOVA as my primary way of specifying mixed ANOVAs, I've hit a stumbling block when it come to adding a covariate to the model. I am using an ANCOVA in order to determine if there is a developmental trajectory in my data; namely, I need to be able to see the

Hello everyone, I am trying to do within subjects repeated measures anova followed by the test of sphericity (sample dataset below). I am able to get either mixed model or linear model anova and TukeyHSD, but have no luck with Repeated-Measures Assuming Sphericity or Separate Sphericity Tests. I am trying to follow example from "car" package, but it seems that I am not getting something

I am trying to reshape data that are in the wide format into the long format. The design is a repeated-measures design, which combined 3 levels of shape (circle, square, triangle) with 3 levels of color (Blue, Red, Green), for a total of 9 variables. The wide data look like this (sorry I couldn't get the columns to line up quite right: Subject CircleBlue CircleRed CircleGreen SquareBlue

Dear All I would need to perform a MANOVA with both fixed (group, sex, group*sex) and random (brood) effects. I wonder if this is at all possible and if R does that. At the moment, I only know that I can run a classic MANOVA with R. Thank you David ______________________________________________ David Costantini, PhD http://www.davidcostantini.it NERC Postdoctoral research associate

Hello everybody, I use the sweetpotato database included in R package: data(sweetpotato) This dataset contains two variables: yield(continous variable) and virus(factor variable). Due to Levene test is significant I cannot assume homogeneity of variances and I apply Welch test in R instead of one-way ANOVA followed by Tukey posthoc. Nevertheless, the problems come from when I apply posthoc

dear all, I want to perform a posthoc test for my ANCOVA: a1<-aov(seeds~treatment*length) With summary(glht(a1, linfct = mcp(treatment = "Tukey"))) R tells me: "covariate interactions found -- please choose appropriate contrast" How do I build these contrasts? Ideally, I would like to have the posthoc test for the ANCOVA including a block-effect

Dear colleagues, In checking a function I am adding to an R package, I get the following warning pair: ... Bad \usage lines found in documentation object 'nominal': "\\method{print}{nominal}"(x, max.print = 10, posthoc = "std.pearson.residuals.sign", assoc = ifelse("univariate" list(c("N", "alpha.X2",

Hello. We have some questions concerning the statistical analysis of a dataset. We aim to compare the sample means of more than 2 independent samples; the sample sizes are unbalanced. The requirements of normality distribution and variance homogeneity were not met even after transforming the data. Thus we applied a nonparametric test: the Kruskal-Wallis-test (H-Test). The null hypothesis was

Hi everyone, I would like to identify the case by groups that is just bigger that avg plus sd. For example, using species as group and petal.wid as my variable in the iris data. What's the better way to doit? creating a function? So,the question is to identify the single element of each species that is just larger than a cut-off point (i.e. larger than mean + sd) I made this, but I can not