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Package: delly (0.9.1-1)

Structural variant discovery by read analysis

Delly performs Structural variant discovery by integrated paired-end and split-read analysis. It discovers, genotypes and visualizes deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read massively parallel sequencing data. It uses paired-ends, split-reads and read-depth to sensitively and accurately delineate genomic rearrangements throughout the genome.

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Download for all available architectures
Architecture Package Size Installed Size Files
amd64 347.1 kB994 kB [list of files]
arm64 325.8 kB870 kB [list of files]
armhf 300.8 kB616 kB [list of files]
ppc64el 360.3 kB1174 kB [list of files]