Search bioRxiv⌕ Search

Biology subjects

Eicher, T. D.

Publications and source records attributed to Eicher, T. D..

2 recordsLinked to original sources

BLOBFISH: Bipartite Limited Subnetworks from Multiple Observations using Breadth-First Search with Constrained Hops

SummaryIn analyzing gene regulatory network models, a common question is how members of a particular set of genes are connected. For example, one might want to explore network relationship between a set of differentially expressed genes, a gene set previously reported in the literature, or elements of one or more pathways. BLOBFISH uses a breadth-first search algorithm adapted to bipartite graphs to identify a compact subnetwork connecting the members of a pre-specified set of genes, providing a regulatory context that can shed light on specific mechanisms involved in a phenotype and its development. We demonstrate the use of BLOBFISH to extract gene regulatory subnetworks reflecting tissue specificity using publicly available data from the Genotype Tissue Expression (GTEx) project.

bioinformatics↗

Finding Salient Multi-Omic Interactomes Relevant to Multiple Biomedical Outcomes using Graph Ensemble Neural Networks

Although multi-omics integration relevant to patient outcome is typically characterized by an analyte interactome, current multi-omic integration methods either (1) model outcome without directly including associations between analytes, (2) model the interactome without directly evaluating the saliency of the model in the context of outcome, or (3) model outcome in a high-dimensional parameter space not suitable for small sample sizes (which are common in multi-omics studies). We introduce Graph Ensemble Neural Network (GENN), a methodology that learns the interactome most predictive of outcome in a low-dimensional parameter space built on complementary attributes for all possible analyte associations (metafeatures). We show that GENN is robust to noise in measurements using a theoretical model, outperforms the predictive performance of existing methods when evaluated on Tegafur drug response in NCI-60 cancer cell line data, and uncovers potentially novel multi-omic mechanisms driving total serum IgE levels in pediatric asthma and patient survival in glioblastomas.

bioinformatics↗