Revision as of 19:09, 15 August 2022 by Israel.herrera (talk | contribs)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search


jasmine website  

This tool is used to merge structural variants (SVs) across samples. Each sample has a number of SV calls, consisting of position information (chromosome, start, end, length), type and strand information, and a number of other values. Jasmine represents the set of all SVs across samples as a network, and uses a modified minimum spanning forest algorithm to determine the best way of merging the variants such that each merged variants represents a set of analogous variants occurring in different samples.

Environment Modules

Run module spider jasmine to find out what environment modules are available for this application.

System Variables

  • HPC_JASMINE_DIR - installation directory
  • HPC_JASMINE_BIN - executable directory