Comments (6)
Hi,
Could you please add the code you used?
I'm thinking that you directly copied this code from the vignette:
reference_hg19_PB = makeIndex(indexPath = '../premadeReferences/',
bsgenome = BSgenome.Hsapiens.UCSC.hg19,
ITR = 'PiggyBac',
targetInsertionSite = 'TTAA', verbose = T)
Can you confirm that there is a folder called premadeReferences at the right place? Try this:
dir.exists('../premadeReferences/')
from tagmeppr.
Yes, I copied the code from the vignette assuming that the imported library ("BSgenome.Hsapiens.UCSC.hg19") would have a premadeReferences folder.
dir.exists('../premadeReferences/') shows that there is no such folder.
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I see. If you are in your preferred working directory (you can test this with getwd()
), you can easily make the other directory with dir.create("premadeReferences")
as a subdirectory of the one you are in now.
from tagmeppr.
I assume that you have BWA installed.
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Thanks,
I was able to map insertions in a mouse ES cell clone of our interest using the code. Will it be possible to continue this thread or a new thread of discussion on these two issues:
- using a different p value as a cut-off?
- using T2T genome assembly for aligning human genome reads? The "BSgenome.Hsapiens.NCBI.T2T.CHM13v2.0" version needs R "4.2", but tagmeppr is not availble for this R version 4.2.
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Great to hear. Yes, please make new issues for those two questions.
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