Supported Applications

NanoVar

  • Description

    a genomic structural variant (SV) caller that utilizes low-depth long-read sequencing such as Oxford Nanopore Technologies (ONT).

  • Installation

    Use the following command to install this title with the CLI client: $ biogrids-cli install nanovar Copy to clipboard
  • Primary Citation*

    C. Y. Tham, R. Tirado-Magallanes, Y. Goh, M. J. Fullwood, B. T. H. Koh, W. Wang, C. H. Ng, W. J. Chng, A. Thiery, D. G. Tenen, and T. Benoukraf. 2020. NanoVar: accurate characterization of patients' genomic structural variants using low-depth nanopore sequencing. Genome Biol. 21(1): 56.


    • *Full citation information available through

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