Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network
Year: 2008
Type: preprint
Abstract: Common hereditary neurodevelopmental disorders such as autism, bipolar disorder, and schizophrenia are most likely both genetically multifactorial and heterogeneous. Because of these characteristics traditional methods for genetic analysis fail when applied to such diseases. To address the problem we propose a novel probabilistic framework that combines the standard genetic linkage formalism with whole-genome molecular-interaction data to predict pathways or networks of interacting genes that contribute to common heritable disorders. We apply the model to three large genotype-phenotype data sets, identify a small number of significant candidate genes for autism (24), bipolar disorder (21), and schizophrenia (25), and predict a number of gene targets likely to be shared among the disorders.
Source: Genome Research
Institutions: Columbia University, University of Chicago
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
Awards: ITR/IM+AP: Automated Compilation and Computational Analysis of Regulatory Networks, SGER: Belief Networks for Human Pathways, Computer System for Functional Analysis of Genomic Data, Acquisition of Transmission Electron Microscope for Interdisciplinary Research, New Approach Towards Mapping of Complex Human Disorders
OpenAlex ID: W2116484405