Supported Applications


  • Description

    is a variant caller for single cell data from whole genome amplification with multiple displacement amplification (MDA). It relies on a pair of samples, where one is from an MDA single cell and the other from a bulk sample of the same cell population, sequenced with any next-generation sequencing technology.

  • Installation

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

    L. J. Dijkstra, J. Köster, T. Marschall, and A. Schönhuth. 2017. Enhancing Sensitivity And Controlling False Discovery Rate In Somatic Indel Discovery Using A Latent Variable Model. bioRxiv.

    • *Full citation information available through

  • Keywords

    Variant Analysis

  • Default Versions

    Linux 64:  0.6.1
    OS X INTEL:  0.6.1