search for: zrl

Dear list: I know this may be an old question. I know how to install the packages to a different directory, for example, /home/zrl/tmp and I know how to load it >library("genefilter",lib.loc="/home/zrl/tmp") but I found some package(for example package A) will have to load some other packages as well, and this time package A will look for the package in the original installation directory not the &quot...

...t know how to) { some codes: initialize an array or list (which one is better?) with "n" elements} #"for" loop for assigning a subset of a large data frame to the elements of the array or list (which on is better?) for (i in 1: n){ array[i] <- df[df$V1==A[i],] } Thanks. ZRL [[alternative HTML version deleted]]

Dear List: I am trying to find a command in R which is like the unix command "less" or "more" to show the data in a object of R. did anyone can help me on this? Is there a collection of such unix-like commands in R? Thanks. -ZRL [[alternative HTML version deleted]]

...lative distance between these sequences and all the genes (genomic sequences) on human genome, i.e., are these sequences locate at upstream of the genes(5 prime end), downstream of the genes(3 prime end) or within the genes. I have about 8000 sequences. Any package, methods could help me? thanks. -zrl [[alternative HTML version deleted]]

Hi, I am wondering how to control the label position on panels of trellise plot. I have 6 panels, I want to all x label positions at the bottom of each panel. How should I do that? Similar, how should I control y label positions of each panel? Thanks. [[alternative HTML version deleted]]

Dear list, I am confused on how to explain the interaction term in the context of "treatment contrast". for example, I have an data frame as below: sub group val 1 a group1 3.685625 2 a group1 3.407445 3 a group1 4.040920 4 a group1 2.890875 5 b group1 3.853280 6 b group1 4.113585 7 b group1 3.043250 8 b group1 3.800920 9 c group1 5.394305 10 c

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