Hi, I'm a new to cnvkit. Thanks for this excellent tool. As it was pointed out in the documentation, CNVkit is primarily designed for use on hybrid capture sequencing data, where off-target reads are present and can be used improve copy number estimates. However, CNVkit can also be used on whole-genome sequencing (WGS) and targeted amplicon sequencing (TAS) datasets by using alternative command-line options.
The batch command supports these workflows through the -m/--method option.
My data are WES sequencing, which method should I choose?--method wgs OR --method hybrid? Hope your reponse.
Hi, I'm a new to cnvkit. Thanks for this excellent tool. As it was pointed out in the documentation, CNVkit is primarily designed for use on hybrid capture sequencing data, where off-target reads are present and can be used improve copy number estimates. However, CNVkit can also be used on whole-genome sequencing (WGS) and targeted amplicon sequencing (TAS) datasets by using alternative command-line options.
The batch command supports these workflows through the -m/--method option.
My data are WES sequencing, which method should I choose?--method wgs OR --method hybrid? Hope your reponse.