{"repository":{"description":"Pindel can detect breakpoints of large deletions, medium sized insertions, inversions, tandem duplications and other structural variants at single-based resolution from next-gen sequence data. It uses a pattern growth approach to identify the breakpoints of these variants from paired-end short reads.","watchers":7,"stargazers":7,"forks":3,"fork":false,"size":508,"owner":"genome","private":false,"open_issues":0,"has_issues":true,"has_downloads":true,"has_wiki":true,"language":"Verilog","created_at":"2013-03-05T12:50:49-08:00","pushed_at":"2013-08-31T20:17:47-07:00","master_branch":"master","organization":"genome"},"actor_attributes":{"type":"User","name":"Kai Ye","company":"The Genome Institute","email":"b23bb55dabbabe161ef030d4e8b044eb08e78938@genome.wustl.edu"},"url":"https://github.com/genome/pindel/compare/4bc1c9a400...bc6d6d6e88"}