[ Source: delly ]
Package: delly (1.1.8-1 and others)
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- Homepage [github.com]
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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 | Version | Package Size | Installed Size | Files |
---|---|---|---|---|
s390x | 1.1.8-1+b2 | 399.0 kB | 1,280.0 kB | [list of files] |