Search bioRxiv⌕ Search

bioRxiv · 10.1101/538579

MAGMA: inference of sparse microbial association networks

Abstract

Microorganisms often live in symbiotic relationship with their environment and they play a central role in many biological processes. They form a complex system of interacting species. Within the gut micro-biota these interaction patterns have been shown to be involved in obesity, diabetes and mental disease. Understanding the mechanisms that govern this ecosystem is therefore an important scientific challenge. Recently, the acquisition of large samples of microbiota data through metabarcoding or metagenomics has become easier. Until now correlation-based network analysis and graphical modelling have been used to identify the putative interaction networks formed by the species of microorganisms, but these methods do not take into account all features of microbiota data. Indeed, correlation-based network cannot distinguish between direct and indirect correlations and simple graphical models cannot include covariates as environmental factors that shape the microbiota abundance. Furthermore, the compositional nature of the microbiota data is often ignored or existing normalizations are often based on log-transformations, which is somewhat arbitrary and therefore affects the results in unknown ways. We have developed a novel method, called MAGMA, for detecting interactions between microbiota that takes into account the noisy structure of the microbiota data, involving an excess of zero counts, overdispersion, compositionality and possible covariate inclusion. The method is based on Copula Gaus-sian graphical models whereby we model the marginals with zero-inflated negative binomial generalized linear models. The inference is based on an efficient median imputation procedure combined with the graphical lasso. We show that our method beats all existing methods in recovering microbial association networks in an extensive simulation study. Moreover, the analysis of two 16S microbial data studies with our method reveals interesting new biology. MAGMA is implemented as an R-package and is freely available at https://gitlab.com/arcgl/rmagma, which also includes the scripts used to prepare the material in this paper.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Cougoul, A. P., Bailly, X., Wit, E. C.. 2019-02-01. MAGMA: inference of sparse microbial association networks. https://doi.org/10.1101/538579

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

KEEP EXPLORING

Related preprints

Deducing splicing events from transcript sets with splicelogic

Long-read RNA sequencing captures a greater proportion of full-length transcripts, enabling more accurate isoform identification, discovery of novel isoforms, and more precise differential transcript usage analysis. However, comparing transcripts, whether between conditions or between sets such as novel and annotated isoforms, yields complex isoform changes that are hard to manipulate, summarize, and visualize. This is compounded by vertical integration of some tools, where downstream analysis depends on the specific output of a particular upstream tool. To address this gap, we have developed splicelogic, an R/Bioconductor package that makes transcript-set comparisons biologically interpretable by turning them into discrete splicing events, such as exon skipping, alternative splice sites, intron retention, and alternative transcription start and end sites. We designed splicelogic to integrate easily with existing RNA-seq workflows and tools. The splicelogic functions are modular, readable, and extensible, making it easy for users to adapt core logic to their own custom scientific questions or novel splicing definitions. By obtaining interpretable splicing events from transcript changes, splicelogic enables downstream analyses, including annotation of RNA-binding protein recognition sites, alongside summary statistics and visualization. The splicelogic package is publicly available and distributed through Bioconductor.

bioinformatics↗

Contrastive Learning Improves Generalization on M2OR Olfactory Binding Dataset

Olfaction-based biosensors stand to have profound impacts in fields such as medical diagnostics, national security, and drug discovery. A promising mode of vapor phase biodetection mimics volatile organic compound-olfactory receptor (VOC-OR) interactions with target-specific protein or peptide probes; however, lack of experimental coverage remains a core bottleneck. Current computational approaches aim to improve prediction of VOC-OR binding to reduce experimental burden, and current machine learning approaches fail to demonstrate a level of generalization that addresses current engineering challenges. Here, using the Molecular to Olfactory Dataset (M2OR) and Insect Olfactory Binding Protein Database (iOBPdb) datasets, data partitioning methods and their performance are evaluated on a neural network and contrastive learning framework on such VOC-OR binding datasets, varying: model training, architecture, and structure of the input data distribution. It was found that holding out certain chemical or proteomic motifs from the training data diminished model performance with a two layer neural network model. The model was able to generalize to state of the art performance (0.88 AUCROC) on every data split by applying a contrastive learning objective defined by shared molecular constituents and a stochastic sampler. This suggests the contrastive objective provides a strong inductive bias for neural networks to predict novel VOC-OR pairs. These findings highlight that model performance on pairwise biological interaction datasets can be inflated through identity leakage from constituent overlap, and emphasize the need for more robust evaluation protocols. Furthermore, we show contrastive regularization mitigates dataset degeneracy through enforcement of compatibility in the models latent geometry that may extend to other binder target-datasets where identity leakage confounds evaluation.

bioinformatics↗

Plate design confounds donor variation and model evaluation in single-cell perturbation screens

Single-cell screens of immune cells from many donors are used to study why individuals respond differently and to benchmark response models. Each donor-perturbation combination typically occupies one well, controls are grouped, and donors share one layout, so technical effects can look biological. Using a 90-cytokine screen, two compound screens, four cohorts and simulations, we show that well effects explain most replicate-control variation in abundant cell types, controls carry a shared offset, and identical control wells differ by hundreds of differentially expressed genes at a standard threshold, about as many as two receptor-negative proteins do. Negative controls, design-aware estimators and perturbation-specific evaluation change the interpretation of four recent analyses. A deep-learning model that scores below a perturbation-agnostic predictor under standard evaluation outperforms a simple baseline on perturbation-specific differences in two of three cell types (significantly in one with stricter controls), but predicts less well the component shared with inert wells.

bioinformatics↗