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Sometimes after running AA and getting ecDNAs, we also want to find some somatic mutations or allele-based CNA and so on, so the RG tag in bam is mostly important ! In order to reuse the bam file from prepareAA, what about adding the function for adding RG tag to the "bwa mem" step ?
I think the results from CNVkit can also be reused for the downstream analysis, so what about adding the information about genes to the "cnvkit batch" step?
The text was updated successfully, but these errors were encountered:
Sometimes after running AA and getting ecDNAs, we also want to find some somatic mutations or allele-based CNA and so on, so the RG tag in bam is mostly important ! In order to reuse the bam file from prepareAA, what about adding the function for adding RG tag to the "bwa mem" step ?
I think the results from CNVkit can also be reused for the downstream analysis, so what about adding the information about genes to the "cnvkit batch" step?
The text was updated successfully, but these errors were encountered: