A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
The current way just dumps all possible header fields inside of the VCF header, but that's not the most efficient and correct way of handling this problem. I need to find some dynamic way to add the correct headers (especially for custom headers added with VCFANNO)
Description of feature
The current way just dumps all possible header fields inside of the VCF header, but that's not the most efficient and correct way of handling this problem. I need to find some dynamic way to add the correct headers (especially for custom headers added with VCFANNO)