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[ 原始碼: delly  ]

套件:delly(1.1.6-1)

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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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硬體架構 套件大小 安裝後大小 檔案
armhf 266。4 kB594。0 kB [檔案列表]