Hello everyone,
We sequenced exomes as well as complete genomes with the HiSeq. We read, that it is recommended to do a GC bias corrrection before starting with CNV-analyses. Can you recommend any tools for that step?
Thanks for your help!
We sequenced exomes as well as complete genomes with the HiSeq. We read, that it is recommended to do a GC bias corrrection before starting with CNV-analyses. Can you recommend any tools for that step?
Thanks for your help!