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...t I get *Code* library(maps) library(geosphere) map("world") xlim <- c(-180.00, 180.00) ylim <- c(-90.00, 90.00) map("world", col = "#f2f2f2", fill = TRUE, bg = "white", lwd = 0.05,xlim = xlim, ylim = ylim) airports <- read.csv("/Users/shabnam/Desktop/airports.csv", as.is=TRUE, header=TRUE) flights <- read.csv("/Users/shabnam/Desktop/flights.csv", as.is=TRUE, header=TRUE) pal <- colorRampPalette(c("#545454", "white"))colors <- pal(100) map("world", col="#303030", fill=TRUE...

Hi, I am using "*Maanova* package" to do anova. I have created *datafile* with probeID as the first column, which is a tab limited text file and also created *designfile*. I have created *readma object* which is named as abf1. >From that readma object, i have to create data object by using *createData*function and also i hav to create model object by using *makemodel* function,

...Number of dyes: 1 Number of arrays: 4 Number of genes: 8799 Number of replicates: 1 Transformation method: None Replicate collapsed: FALSE > data(abf1) > abf1 <- *createData*(abf1, 1, log.trans=F) *Error: *could not find function* "createData" * Shabnam K. [[alternative HTML version deleted]]

..., ...) : coercing argument of type 'double' to logical 4: In FUN(newX[, i], ...) : coercing argument of type 'double' to logical 5: In digamma(df/2) : NaNs produced 6: In digamma(df/2) : NaNs produced 7: In digamma(df/2) : NaNs produced 8: In digamma(df/2) : NaNs produced Shabnam K. [[alternative HTML version deleted]]

...Language (Joshua Wiley) 19. Re: how to calculate the product of every two elements in two vectors (Gabor Grothendieck) 20. Re: Book on R's Programming Language (Joseph Magagnoli) 21. Re: Constrain density to 0 at 0? (Greg Snow) 22. matest function for multiple factors (shabnam k) 23. Re: How to deal with more than 6GB dataset using R? (Greg Snow) 24. Using R to fill ETM+ data gaps? (Abdi, Abdulhakim) 25. How to generate a sequence of dates without hardcoding the year (Felipe Carrillo) 26. Re: How to generate a sequence of dates without hardcoding...

Hi, I have taken one microarray experiment and trying to implement same statistical measures what they have done.I have taken datasets from GEO platform with accession number GSE1557. In the experiment,about half of double transgenic rats (dTGR) over-expressing the human renin and angiotensinogen genes die by age 7 weeks of terminal heart failure (THF); the other (preterminal) half develops

Hi, Am using maanova package for doing anova.But am getting error like this..plz, help me regarding this.. > TGR=read.madata("rmaexpr.dat",designfile="design.dat") Reading one color array. Otherwise change arrayType='twoColor' then read the data again Warning messages: 1: In read.madata("rmaexpr.dat", designfile = "design.dat") : Assume that

Hi there; Although I have seen a few people had the same problem but can't figure out eventually what they have done to resolve it! This is why I ask this again. I have configured rsync to be run as a daemon server and run the following command line. What could be wrong that I get this error: [I have no problem with the reverse function, I mean if we call this one as 'put' I can