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[ 源代码: delly  ]

软件包: delly (0.8.2-1)

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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下载可用于所有硬件架构的
硬件架构 软件包大小 安装后大小 文件
amd64 250.9 kB896 kB [文件列表]
armhf 204.6 kB542 kB [文件列表]