Entering edit mode
11.5 years ago
Plantae
▴
390
hi, all,
i try to find CNVs from a high-depth resequenced sample (>30x), which is a plant species.
however, several CNV detect tools could only be used for human genomes,
i am wondering if there are some standalone tools that can get gc-corrected read counts using BAM file as inputs.
then we can use call CNVs based on these corrected values.