An ultra-fast and sensitive structural variant detection tool for long-read sequencing data.
Kled is designed to call SVs nicely and quickly using long-read sequencing data. It takes mapped reads file (bam) as input and reports SVs to the stdout in the VCF file format. Kled can yield precise and comprehensive SV detection results within minutes and can run on any modern computer without needing of any field knowledge of the user to perform the SV detection.
