cnv_facets
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Somatic copy variant caller (CNV) for next generation sequencing
I get the vcf file form cnv_facets I use the WGS data I wonder How can I get the segment data from the vcf data especially the column of number...
I have the bam files of a tumour sample "T11QM0022" and its matched normal sample "B11QM0022". They were generated using the GATK4 Best Practices pipeline. They are sorted and index....
Hi, I test CNV_Facets with exome data and get squares instead of letters on png file. I tried different versions of the container, getting the same result. Do you have...
I recently installed cnv_facets with the following instructions in my University's HPC cluster: mamba create -n my_project mamba activate my_project mamba install -c bioconda -c conda-forge cnv_facets The installation works...
When trying to run `cnv_facets.R -h`, I get the error: ``` Error: package or namespace load failed for ‘ggplot2’ in loadNamespace(j 1.0.1 is required Execution halted ``` When I run...
Hi, I am using the latest biocontainer with cnv_facets: 0.16.1 installed. From a set of 11 samples, I just have one sample that has the issue pasted below when the...
Is there any way to use reference genomes of organisms other than hg19, hg38, mm9, and mm10? I am trying to use facets for dog samples (canFam3) and the first...