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Delly

  • Description

    Delly is an integrated structural variant (SV) prediction method that can discover, genotype and visualize 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. Structural variants can be visualized using Delly-maze and Delly-suave.

  • Usage

    To list all executables provided by Delly, run: $ biogrids-list delly Copy to clipboard

  • Installation

    Use the following command to install this title with the CLI client: $ biogrids-cli install delly Copy to clipboard Available operating systems: Linux 64, OS X INTEL

  • Primary Citation*

    T. Rausch, T. Zichner, A. Schlattl, A. M. Stütz, V. Benes, and J. O. Korbel. 2012. DELLY: structural variant discovery by integrated paired-end and split-read analysis. Bioinformatics. 28(18): i333-i339.


    • *Full citation information available through

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