There are 4 repositories under structural-variations topic.
Structural variation caller using third generation sequencing
Toolset for SV simulation, comparison and filtering
NGMLR is a long-read mapper designed to align PacBio or Oxford Nanopore (standard and ultra-long) to a reference genome with a focus on reads that span structural variations
Application of pan-genome for population
novoBreak: local assembly for breakpoint detection in cancer genomes
Micro DNA identification
A framework to annotate SVs with previous known SVs (vcf file) and or with genomic features (gff and or bed files)
MAMnet uses a deep learning network to call genetic variants from third generation DNA sequencing data.
A snakemake pipeline to call structure variants from ONT data
Pipeline for SV detection using 10X genomics data