CNV callers for WES data
Hello,
I want to call somatic CNVs for Whole Exome Sequencing data. These are tumor samples, with no normal/control samples available. I read this article and tried a couple of tools like ADTEX and ExomeCNV, however they require normal samples to be provided as well. I cannot run with just tumor samples.
I would really appreciate some recommendations for tools I can try.
Thank you.
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