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2.9 years ago
manojkumarbioinfo
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100
Hi, I'm using cnv kit for my copy number variant analysis, I'm facing some issues whenever I call CNV my gene names are combined together for example as shown in the image below
does anyone know to fix this issue? I'm using target sequencing
command usedÂ
python cnvkit.py batch my.bam --targets my_targets.bed -n --fasta hg38.fa --output-dir test_run --diagram --scatter --diagram --annotate refFlat.txt --access access-10kb.m10.bed
I don't get your problem. If you have a CNV in "chr3:72230415-91426092", you'll overlap 3 genes: RYBP, SHQ1, EPHA3.
I don't want the gene name and location to be combined. I want to be separate for example RYBP chromosome start - end its log-ratio.
You can use
call
function usingTumor.cnr
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