similar to: Interpretation of davies.test() in segmented package

Hi Everyone, I am trying to use lmFit function; however, i cannot find it function anywhere. I have been trying to find the function in Bioconductor and elsewhere. I re-install bioconductor source, update package and update R as well. no luck Is there a command in R where i can just type, and it will download it for me? -- View this message in context:

I'm new to R and some what new to the world of stats. I got frustrated with excel and found R. Enough of that already. I'm trying to test and correct for Heteroskedasticity I have data in a csv file that I load and store in a dataframe. > ds <- read.csv("book2.csv") > df <- data.frame(ds) I then preform a OLS regression: > lmfit <- lm(df$y~df$x) To

I try to send this message To Gordon Smyth at smyth at vehi,edu.au but it bounced back, so here it is to r-help I am trying to use limma, just downloaded it from CRAN. I use R 2.0.1 on Win XP see the following: > library(RODBC) > chan1 <- odbcConnectExcel("D:/Data/mgc/Chips/Chips4.xls") > dd <- sqlFetch(chan1,"Raw") # all data 12000 > # > nzw <-

Hi there, I am trying to use linear regression to solve the following equation - y <- c(0.2525, 0.3448, 0.2358, 0.3696, 0.2708, 0.1667, 0.2941, 0.2333, 0.1500, 0.3077, 0.3462, 0.1667, 0.2500, 0.3214, 0.1364) x2 <- c(0.368, 0.537, 0.379, 0.472, 0.401, 0.361, 0.644, 0.444, 0.440, 0.676, 0.679, 0.622, 0.450, 0.379, 0.620) x1 <- 1-x2 # equation lmFit <- lm(y ~ x1 + x2) lmFit Call:

Hi all,   I have loaded the LIMMA and Biobase package and tried these commands:   library(limma) library("Biobase") data <- read.table("c:/temp/data.txt",header=T,row.names=1) ExpressionData <- as.matrix(data[,c(2,3,4,6,7,8)]) eset <- new("ExpressionSet", exprs = ExpressionData) design <- cbind(WT=1,P=c(0,1,1,0,1,1),G=c(0,1,0,0,1,0)) fit <-

Hallo, > fit12<-lmFit(qrg[,1:2]) > t12<-toptable(fit12,adjust="fdr",number=25,genelist=qrg$genes[,1]) > t12 ID logFC t P.Value adj.P.Val B 522 PLAU_OP -6.836144 -8.420414 5.589416e-05 0.01212520 2.054965 1555 CD44_WIZ -6.569622 -8.227938 6.510169e-05 0.01212520 1.944046 Can anyone tell me what the difference is between P.Value

Hi, I have two data set of normalized Affymetrix CEL files, wild type vs Control type.(each set have further three replicates). > wild.fish AffyBatch object size of arrays=712x712 features (10 kb) cdf=Zebrafish (15617 affyids) number of samples=3 number of genes=15617 annotation=zebrafish notes= > Dicer.fish AffyBatch object size of arrays=712x712 features (10 kb) cdf=Zebrafish (15617

Hello, I would like to fit a linear regression and when I use summary(), I got the following result: Call: lm(formula = weight ~ group - 1) Residuals: Min 1Q Median 3Q Max -1.0710 -0.4938 0.0685 0.2462 1.3690 Coefficients: Estimate Std. Error t value Pr(>|t|) groupCtl 5.0320 0.2202 22.85 9.55e-15 *** groupTrt 4.6610 0.2202 21.16 3.62e-14

On Wed, December 22, 2004 12:11 am, r.ghezzo at staff.mcgill.ca said: > ----- Forwarded message from r.ghezzo at staff.mcgill.ca ----- > Date: Mon, 20 Dec 2004 15:45:11 -0500 > From: r.ghezzo at staff.mcgill.ca > Reply-To: r.ghezzo at staff.mcgill.ca > Subject: [R] problems with limma > To: r-help at stat.math.ethz.ch > > I try to send this message To Gordon

I know this has got to be simple, but I have a added an arrow to a graph with: arrows(5,8,8, predict(lmfit,data.frame(x=8)), length=0.1) but its in the wrong position, correcting it and running again adds an new arrow (which is what you would expect) so how do I a) edit the existing arrow, and b) delete it all together As so often seems to be the case, some of the simplist things seem also to

>>>>> Andrew Robinson via R-help >>>>> on Thu, 14 Nov 2024 12:45:44 +0000 writes: > Not a direct answer but you may find lm.fit worth > experimenting with. Yes, lm.fit() is already faster, and .lm.fit() {added to base R by me, when a similar question was asked years ago ...} is even an order of magnitude faster in some cases. See

What is the way to add an arbitrary fit from a model to a lattice conditioning plot ? For example xyplot(v1 ~v2 | v3,data=mydata, panel=function(...){ panel.xyplot(...) panel.loess(...,col.line="red") } ) Will add a loess smoother. Instead, I want to put a fit from lm (but not a simple straight line) and the fit has to be done for each panel

I'm looking for guidance on how to implement forward stepwise regression using lmStepAIC in Caret. The stepwise "direction" appears to default to "backward". When I try to use "scope" to provide a lower and upper model, Caret still seems to default to "backward". Any thoughts on how I can make this work? Here is what I tried: itemonly <-

Dear R users, I'am using marray and Limma packages to analyze genepix output. 1) how can I filter bad spots from my data (data contains 3 types of bad spots). my experiment contains 12 samples and the bad spot are not associated to the same probes 2) how can I remove control probes from my data ? I'm sorry, i'm new with R and I can't find answer in packages doc. best regards,

Hello, I am trying to run a code (see reference section) and when I run the line: fit<-lmFit(xen1dataeset,design), I get the error message: Error in lm.fit(design, t(M)) : incompatible dimensions I will really appreciate if someone can help me understand this error message and possibly help me debug the problem. Thanks manisha Reference section xen1data<-ReadAffy()

Hi I am using the ggplot2 package for the volcano plot and I am using the following code for the same: g = ggplot(data=data, aes(x=data[11], y=-log10(data[12]), colour=threshold)) + + geom_point(alpha=0.4, size=1.75) + + opts(legend.position = "none") + + xlim(c(-10, 10)) + ylim(c(0, 15)) + + xlab("log2 fold change") + ylab("-log10 p-value") data[11] is a

For an application of ridge regression, I need to get the covariance matrices of the estimated regression coefficients in addition to the coefficients for all values of the ridge contstant, lambda. I've studied the code in MASS:::lm.ridge, but don't see how to do this because the code is vectorized using one svd calculation. The relevant lines from lm.ridge, using X, Y are:

I would like to fit regression models of the form y ~ ns(x, df=splineDF) where splineDF is passed as an argument to a wrapper function. This works fine if the regression function is lm(). But with lme(), I get two different errors, depending on how I handle splineDF inside the wrapper function. A workaround is to turn the lme() command, along with the appropriate value of splineDF, into a text

Hi, I am relatively new to R and Bioconductor and am trying to filter the topTable that I generated of differentially expressed genes from my normlized eset file comprised of ~ 40 HG-133A Affy microarrays . I would like to see if particular probesets are represented in this list. Alternatively I would like to generate a topTable of differentially expressed genes using only specified probesets

Hello, I'm trying to do some non-linear regression with 2 cell types and 4 tissue type treatments using selfStart models Following Ritz and Streibig (2009), I wrote the following routines: ##Selfstart expDecayAndConstantInflowModel <- function(Tb0, time, aL, aN, T0){ exp(-time*aL)*(T0*aL+(-1+exp(time * aL))*Tb0 * aN)/aL } expDecayAndConstantInflowModelInit <- function(mCall, LHS,