<![CDATA[BOL: JASMINE: Jointly Accurate Sv Merging with Intersample Network Edges]]> https://bioinformaticsonline.com/bookmarks/view/43904/jasmine-jointly-accurate-sv-merging-with-intersample-network-edges? https://bioinformaticsonline.com/bookmarks/view/43904/jasmine-jointly-accurate-sv-merging-with-intersample-network-edges Sat, 02 Jul 2022 11:41:53 -0500 https://bioinformaticsonline.com/bookmarks/view/43904/jasmine-jointly-accurate-sv-merging-with-intersample-network-edges <![CDATA[JASMINE: Jointly Accurate Sv Merging with Intersample Network Edges]]> 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.

Address of the bookmark: https://github.com/mkirsche/Jasmine

]]> Shruti Paniwala