bioRxiv Science⌕ Search

bioRxiv · 10.1101/075069

Solving the influence maximization problem reveals regulatory organization of the yeast cell cycle.

Abstract

The Influence Maximization Problem (IMP) aims to discover the set of nodes with the greatest influence on network dynamics. The problem has previously been applied in epidemiology and social network analysis. Here, we demonstrate the application to cell cycle regulatory network analysis of Saccharomyces cerevisiae.\n\nFundamentally, gene regulation is linked to the flow of information. Therefore, our implementation of the IMP was framed as an information theoretic problem on a diffusion network. Utilizing all regulatory edges from YeastMine, gene expression dynamics were encoded as edge weights using a variant of time lagged transfer entropy, a method for quantifying information transfer between variables. Influence, for a particular number of sources, was measured using a diffusion model based on Markov chains with absorbing states. By maximizing over different numbers of sources, an influence ranking on genes was produced.\n\nThe influence ranking was compared to other metrics of network centrality. Although top genes from each centrality ranking contained well-known cell cycle regulators, there was little agreement and no clear winner. However, it was found that influential genes tend to directly regulate or sit upstream of genes ranked by other centrality measures. This is quantified by computing node reachability between gene sets; on average, 59% of central genes can be reached when starting from the influential set, compared to 7% of influential genes when starting at another centrality measure.\n\nThe influential nodes act as critical sources of information flow, potentially having a large impact on the state of the network. Biological events that affect influential nodes and thereby affect information flow could have a strong effect on network dynamics, potentially leading to disease.\n\nCode and example data can be found at: https://github.com/Gibbsdavidl/miergolf\n\nAuthor SummaryThe Influence Maximization Problem (IMP) is general and is applied in fields such as epidemiology, social network analysis, and as shown here, biological network analysis. The aim is to discover the set of regulatory genes with the greatest influence in the network dynamics. As gene regulation, fundamentally, is about the flow of information, the IMP was framed as an information theoretic problem. Dynamics were encoded as edge weights using time lagged transfer entropy, a quantity that defines information transfer across variables. The information flow was accomplished using a diffusion model based on Markov chains with absorbing states. Ant optimization was applied to solve the subset selection problem, recovering the most influential nodes.The influential nodes act as critical sources of information flow, potentially affecting the network state. Biological events that impact the influential nodes and thereby affecting normal information flow, could have a strong effect on the network, potentially leading to disease.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

David Gibbs, Ilya Shmulevich. 2016-09-14. Solving the influence maximization problem reveals regulatory organization of the yeast cell cycle.. https://doi.org/10.1101/075069

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Detection and assembly of novel sequence insertions using Linked-Read technology

MotivationEmerging Linked-Read (aka read-cloud) technologies such as the 10x Genomics Chromium system have great potential for accurate detection and phasing of largescale human genome structural variations (SVs). By leveraging the long-range information encoded in Linked-Read sequencing, computational techniques are able to detect and characterize complex structural variations that are previously undetectable by short-read methods. However, there is no available Linked-Read method for detection and assembly of novel sequence insertions, DNA sequences present in a given sequenced sample but missing in the reference genome, without requiring whole genome de novo assembly. In this paper, we propose a novel integrated alignment-based and local-assembly-based algorithm, Novel-X, that effectively uses the barcode information encoded in Linked-Read sequencing datasets to improve detection of such events without the need of whole genome de novo assembly. We evaluated our method on two haploid human genomes, CHM1 and CHM13, sequenced on the 10x Genomics Chromium system. These genomes have been also characterized with high coverage PacBio long-reads recently. We also tested our method on NA12878, the wellknown HapMap CEPH diploid genome and the child genome in a Yoruba trio (NA19240) which was recently studied on multiple sequencing platforms. Detecting insertion events is very challenging using short reads and the only viable available solution is by long-read sequencing (e.g. PabBio or ONT). Our experiments, however, show that Novel-X finds many insertions that cannot be found by state of the art tools using short-read sequencing data but present in PacBio data. Since Linked-Read sequencing is significantly cheaper than long-read sequencing, our method using Linked-Reads enables routine large-scale screenings of sequenced genomes for novel sequence insertions. AvailabilitySoftware is freely available at https://github.com/1dayac/novel_insertions Contactimh2003@med.cornell.edu Supplementary informationSupplementary data are available at https://github.com/1dayac/novel_insertions_supplementary

Bioinformatics↗

iCARE: An R Package to Build and Apply Absolute Risk Models

This report describes a R package, called the Individualized Coherent Absolute Risk Estimation (iCARE) tool, that allows researchers to build and evaluate models for absolute risk and apply them to estimate an individuals risk of developing disease during a specified time interval based on a set of user defined input parameters. An attractive feature of the software is that it gives users flexibility to update models rapidly based on new knowledge on risk factors and tailor models to different populations by specifying three input arguments: (1) a model for relative risk, (2) an age-specific disease incidence rate, (3) the distribution of risk factors for the population of interest. The tool can handle missing information on risk factors for individuals for whom risks are to be predicted using a coherent approach where all estimates are derived from a single model after appropriate model averaging. The software allows single nucleotide polymorphisms (SNPs) to be incorporated into the model using published odds ratios and allele frequencies. The validation component of the software implements the methods for evaluation of model calibration, discrimination and risk-stratification based on independent validation datasets. We provide an illustration of the utility of iCARE for building, validating and applying absolute risk models using breast cancer as an example.

Bioinformatics↗

deSPI: efficient classification of metagenomic reads with lightweight de Bruijn graph-based reference indexing

SummaryIn metagenomic studies, fast and effective tools are on wide demand to implement taxonomy classification for upto billions of reads. Herein, we propose deSPI, a novel read classification method that classifies reads by recognizing and analyzing the matches between reads and reference with de Bruijn graph-based lightweight reference indexing. deSPI has faster speed with relatively small memory footprint, meanwhile, it can also achieve higher or similar sensitivity and accuracy.\n\nAvailabilitythe C++ source code of deSPI is available at https://github.com/hitbc/deSPI\n\nContactydwang@hit.edu.cn\n\nSupplementary informationSupplementary data are available at Bioinformatics online.

Bioinformatics↗