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[ Bron: delly  ]

Pakket: delly (1.1.8-1 en anderen)

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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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Platform Versie Pakketgrootte Geïnstalleerde grootte Bestanden
armel 1.1.8-1+b2 318,5 kB1.027,0 kB [overzicht]