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frameschr1
2010 Oct 01
1
[Help]:How to use "loop" to achieve this aim?
Hello, Everyone,
how to use "loop" to make the process automatic and fast?
When compute each sample, the script type in R almost the same, just the
input and output file's name is changed(chr1 change to chr2, chr3,chr4...).
The first sample's script like this:
>chr1=MEDIPS.readAlignedSeqences(BSgenome="hg19", file="chr1",numrows= )