An improved probabilistic disease-association method to identify common and rare disease associated variants from large-scale case/control association studies by next-generation sequencing

Author: Francisco M. De La Vega, et al, Fabric Genomics

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Date: July 25, 2018

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Read how VVP outperforms other methods to score genetic variants with respect to their disease-causing potential, whether they are coding or non-coding, leveraging population-scale databases. Coupled with Fabric Genomics platform, VVP facilitates fast and accurate genetic disease diagnostics sequencing data.