Method And System For Network Modeling To Enlarge The Search Space Of Candidate Genes For Diseases

Abstract

With the advent of low cost, high-throughput whole genome sequencing (“next generation sequencing”), tools are available to assay human genetic variation contributing to inherited disease syndromes. A method is disclosed for prioritization of genetic variants, and identification of disease genes, using network modeling of gene associations.


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Document History
  • Publication: Jul 9, 2019
  • Application: Jun 18, 2012
    US US 201213526317 A
  • Priority: Jun 18, 2012
    US US 201213526317 A
  • Priority: Jun 16, 2011
    US US 201161497542 P

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