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

Keystone Symposium: One Million Genomes: From Discovery to Health 2018 Poster

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

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Steven Flygare, Edgar Javier Hernandez, Lon Phan, Barry Moore, Man Li, Anthony Fejes, Hao Hu, Karen Eilbeck, Chad Huff, Lynn Jorde, Martin G. Reese and Mark Yandell

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.