Search bioRxivSearch

bioRxiv · 10.1101/030650

ADAGE analysis of publicly available gene expression data collections illuminates Pseudomonas aeruginosa-host interactions

Abstract

The growth in genome-scale assays of gene expression for different species in publicly available databases presents new opportunities for computational methods that aid in hypothesis generation and biological interpretation of these data. Here, we present an unsupervised machine-learning approach, ADAGE (Analysis using Denoising Autoencoders of Gene Expression) and apply it to the interpretation of all of the publicly available gene expression data for Pseudomonas aeruginosa, an important opportunistic bacterial pathogen. In post-hoc positive control analyses using curated knowledge, the P. aeruginosa ADAGE model found that co-operonic genes often participated in similar processes and accurately predicted which genes had similar functions. By analyzing newly generated data and previously published microarray and RNA-seq data, the ADAGE model identified gene expression differences between strains, modeled the cellular response to low oxygen, and predicted the involvement of biological processes despite low level expression differences in directly involved genes. Comparison of ADAGE with PCA and ICA revealed that ADAGE extracts distinct signals. We provide the ADAGE model with analysis of all publicly available P. aeruginosa GeneChip experiments, and we provide open source code for use in other species and settings.

Source connections

Explore related subjects

Keep this discovery

BibTeXRIS

Jie Tan, John H Hammond, Deborah A Hogan, Casey S Greene. 2015-11-05. ADAGE analysis of publicly available gene expression data collections illuminates Pseudomonas aeruginosa-host interactions. https://doi.org/10.1101/030650

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

KEEP EXPLORING

Related preprints

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

De novo assembly of viral quasispecies using overlap graphs

A viral quasispecies, the ensemble of viral strains populating an infected person, can be highly diverse. For optimal assessment of virulence, pathogenesis and therapy selection, determining the haplotypes of the individual strains can play a key role. As many viruses are subject to high mutation and recombination rates, high-quality reference genomes are often not available at the time of a new disease outbreak. We present SAVAGE, a computational tool for reconstructing individual haplotypes of intrahost virus strains without the need for a high-quality reference genome. SAVAGE makes use of either FM-index based data structures or ad-hoc consensus reference sequence for constructing overlap graphs from patient sample data. In this overlap graph, nodes represent reads and/or contigs, while edges reflect that two reads/contigs, based on sound statistical considerations, represent identical haplotypic sequence. Following an iterative scheme, a new overlap assembly algorithm that is based on the enumeration of statistically well-calibrated groups of reads/contigs then efficiently reconstructs the individual haplotypes from this overlap graph. In benchmark experiments on simulated and on real deep coverage data, SAV-AGE drastically outperforms generic de novo assemblers as well as the only specialized de novo viral quasispecies assembler available so far. When run on ad-hoc consensus reference sequence, SAVAGE performs very favorably in comparison with state-of-the-art reference genome guided tools. We also apply SAVAGE on two deep coverage samples of patients infected by the Zika and the hepatitis C virus, respectively, which sheds light on the genetic structures of the respective viral quasispecies.

Bioinformatics