Year: 2015
Type: article
Abstract: Background Genes work in concert as a system, not as independent entities, to mediate disease states. There has been considerable interest in understanding variations in molecular signatures between normal and disease states. The selective-voting convex-hull ensemble procedure accommodates molecular heterogeneity within and between groups and allows retrieval of sample-specific sets and investigation of variations in individual networks relevant to personalized medicine[1]. The work here describes using the convex-hull voting method on a large data set. Using parallelization techniques, we predict that we can execute the convex-hull voting algorithm on the University of Kentucky cluster (DLX) using a dataset much too large to run in a feasible time on a single machine.
Source: BMC Bioinformatics
Authors: Sally R Ellingson, Chi Wang, Radhakrishnan Nagarajan
Institutions: University of Kentucky, Markey Cancer Center
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,990
Funder: University of Kentucky
Award: G6888208216
OpenAlex ID: W2366839226
