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Hello;
I would like to know if you are still working on the development to support WES data.
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Hi,
I am currently attempting to perform an association analysis on noncoding regions using WES data. However, while executing 379 array jobs, some of the jobs failed with an error. Could this iss…
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**Describe the solution you'd like**
Hi,
Do you have specific plans to add WES support? Can you tell us about any dates when to expect it?
Best, Anna
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Dear,
I am running CNVkit to call cnvs on samples sequenced with WES sequencing, and get an error below:
`Segmenting with method 'cbs', significance threshold 0.0001, in 1 processes
Traceback (mo…
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#include
int main()
{printf("shis");
return 0;
}
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### Description of the bug
Hi Developers,
I'm trying to run the Sarek implemented ASCAT for CNV analysis on WES data. On the nfcore Sarek website, it's suggested to follow 5 steps, as specified in…
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Issue requested by Wes following discussion in .
Pandas has an extension system which allows users to create [custom accessors](https://pandas.pydata.org/pandas-docs/stable/development/extending.html…
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Do you have any doubts about counting the coverage for the entire reference genes, even though, for WES, the coverage is present only in the coding regions?
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Hi,
Thank you for this great tool.
I have a question with regard to SNV calling in paraloguous regions for WES/WGS illumina models.
As i understand, by default, candidates variants in regions with …
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I would like to run QDNAseq on whole exome sequencing data (captured using SureSelect Human All Exon platform which covers about 50MB of the human exonic regions). Knowing this, how can I modify the Q…