Like #1 I also can't understand how to create the input files. Let's assume that I've downloaded a few VCFs of TCGA Cancer Samples from Genomic Data Commons. How can I easily analyse them with Spruce? The user experience is an important factor in how popular a method becomes and how often it will be cited. Spruce could improve.
Like #1 I also can't understand how to create the input files. Let's assume that I've downloaded a few VCFs of TCGA Cancer Samples from Genomic Data Commons. How can I easily analyse them with Spruce? The user experience is an important factor in how popular a method becomes and how often it will be cited. Spruce could improve.