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Annotation using different database #350

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jennyp76 opened this issue Feb 8, 2024 · 1 comment
Open

Annotation using different database #350

jennyp76 opened this issue Feb 8, 2024 · 1 comment

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@jennyp76
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jennyp76 commented Feb 8, 2024

Hi,
First of all, thank you for the wonderful tool. It been a lot of help.

I am trying to compare the total copy number between PureCN and CNVkit based on genes.
So, comparing the total copy number of a gene detected from PureCN and CNVkit.
Therefore, keeping the database used for annotation should be the same.

  1. Would there be a method to annotate genes using the 4th column of the BED file instead of TxDb.Hsapiens.UCSC.hg38.knownGene R package?
  2. And it this "https://hgdownload.soe.ucsc.edu/gbdb/hg38/knownGene.txt" is the annotation file used in PureCN for annotation?

Thanks, jen

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To Reproduce
Copy and paste your complete command line arguments from PureCN.R. If possible and potentially relevant, also copy the output of NormalDB.R and Coverage.R.

Expected behavior
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Log file
Please copy and paste the log file (Sampleid.log) of a representative example

B-allele frequency plot
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(Sampleid.pdf).

Session Info
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@lima1
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lima1 commented Feb 8, 2024

That's a valid feature request. I'll see when I have time for this. If urgent, you probably for now are faster correcting the interval file gene column manually.

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