Structural variation caller using third generation sequencing
DELLY2: Structural variant discovery by integrated paired-end and split-...
Structural variant and indel caller for mapped sequencing data
Structural variant toolkit for VCFs
Long read based human genomic structural variation detection with cuteSV
structural variant calling and genotyping with existing tools, but, smoo...
Fast and accurate gene fusion detection from RNA-Seq data
A structural variation pipeline for short-read sequencing
Graph realignment tools for structural variants
Pipeline for calling structural variations in whole genomes sequencing O...
don't get DUP'ed or DEL'ed by your putative SVs.
A method for variant graph genotyping based on exact alignment of k-mers
Toolkit for calling structural variants using short or long reads
simuG: a general-purpose genome simulator