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Pindel

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.

homepage: http://gmt.genome.wustl.edu/packages/pindel/

version toolchain
0.2.5b8 foss/2016b
0.2.5b9-20170508 GCC/11.2.0
0.2.5b9-20170508 GCC/11.3.0
0.2.5b9-20170508 GCC/6.4.0-2.28

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