Package: delly (0.8.1-2)
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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 delly
Architecture | Package Size | Installed Size | Files |
---|---|---|---|
armhf | 197.3 kB | 546.0 kB | [list of files] |