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MarViN

  • Description

    a method for rapid genotype refinement for whole-genome sequencing data using multi-variate normal distribution. Whole-genome low-coverage sequencing has been combined with linkage-disequilibrium (LD) based genotype refinement to accurately and cost-effectively infer genotypes in large cohorts of individuals.

  • Usage

    To list all executables provided by MarViN, run: $ biogrids-list marvin Copy to clipboard

  • Installation

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

  • Primary Citation*

    R. Arthur, J. O'Connell, O. Schulz-Trieglaff, and A. J. Cox. 2016. Rapid genotype refinement for whole-genome sequencing data using multi-variate normal distributions. Bioinformatics. 32(15): 2306-2312.


    • *Full citation information available through

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