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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.
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?
Describe the issue
A clear and concise description of what the issue is.
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
A clear and concise description of what you expected to happen.
Log file
Please copy and paste the log file (Sampleid.log) of a representative example
B-allele frequency plot
Please take a screenshot of the B-allele frequency plot of the maximum likelihood solution
(Sampleid.pdf).
Session Info
Please start R, type sessionInfo() and paste the output.
The text was updated successfully, but these errors were encountered:
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.
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.
Thanks, jen
Describe the issue
A clear and concise description of what the issue is.
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
A clear and concise description of what you expected to happen.
Log file
Please copy and paste the log file (Sampleid.log) of a representative example
B-allele frequency plot
Please take a screenshot of the B-allele frequency plot of the maximum likelihood solution
(Sampleid.pdf).
Session Info
Please start R, type sessionInfo() and paste the output.
The text was updated successfully, but these errors were encountered: