Hi,
Does anyone has experience to use CNV-seq to detect copy number variation?
I want to know that CNV-Seq run with DNA-seq or RNA-seq?
Because I have RNA-seq of tumor paired-end from illumina ,can I use it to run CNV-seq?
Thanks!!
Does anyone has experience to use CNV-seq to detect copy number variation?
I want to know that CNV-Seq run with DNA-seq or RNA-seq?
Because I have RNA-seq of tumor paired-end from illumina ,can I use it to run CNV-seq?
Thanks!!
Comment