SVIM v1.1.1

Stable release 1.1.1

Changelog:

• Output breakends (BND) in VCF file
• Detect large tandem duplications even if they are not spanned by a single read (add flag not_fully_covered)
• Add new command line option to skip genotyping
• Make VCF output more flexible:
  • Let user choose which SV types to include in VCF output
  • Let user choose how to represent tandem and interspersed duplications (either as DUP or as INS)
• Add scatter plot of read support for reference and variant allele (see below)