Biology subjects

Reiman, D.

Publications and source records attributed to Reiman, D..

4 recordsLinked to original sources

bioRxiv2020

Inferring cellular trajectories from scRNA-seq using Pseudocell Tracer

Single cell RNA sequencing (scRNA-seq) can be used to infer a temporal ordering of dynamic cellular states. Current methods for the inference of cellular trajectories rely on unbiased dimensionality reduction techniques. However, such biologically agnostic ordering can prove difficult for modeling complex developmental or differentiation processes. The cellular heterogeneity of dynamic biological compartments can result in sparse sampling of key intermediate cell states. This scenario is especially pronounced in dynamic immune responses of innate and adaptive immune cells. To overcome these limitations, we develop a supervised machine learning framework, called Pseudocell Tracer, which infers trajectories in pseudospace rather than in pseudotime. The method uses a supervised encoder, trained with adjacent biological information, to project scRNA-seq data into a low-dimensional cellular state space. Then a generative adversarial network (GAN) is used to simulate pesudocells at regular intervals along a virtual cell-state axis. We demonstrate the utility of Pseudocell Tracer by modeling B cells undergoing immunoglobulin class switch recombination (CSR) during a prototypic antigen-induced antibody response. Our results reveal an ordering of key transcription factors regulating CSR, including the concomitant induction of Nfkb1 and Stat6 prior to the upregulation of Bach2 expression. Furthermore, the expression dynamics of genes encoding cytokine receptors point to the existence of a regulatory mechanism that reinforces IL-4 signaling to direct CSR to the IgG1 isotype.

bioinformatics↗

bioRxiv2020

Using Conditional Generative Adversarial Networks to Boost the Performance of Machine Learning in Microbiome Datasets

The microbiome of the human body has been shown to have profound effects on physiological regulation and disease pathogenesis. However, association analysis based on statistical modeling of microbiome data has continued to be a challenge due to inherent noise, complexity of the data, and high cost of collecting large number of samples. To address this challenge, we employed a deep learning framework to construct a data-driven simulation of microbiome data using a conditional generative adversarial network. Conditional generative adversarial networks train two models against each other while leveraging side information learn from a given dataset to compute larger simulated datasets that are representative of the original dataset. In our study, we used a cohorts of patients with inflammatory bowel disease to show that not only can the generative adversarial network generate samples representative of the original data based on multiple diversity metrics, but also that training machine learning models on the synthetic samples can improve disease prediction through data augmentation. In addition, we also show that the synthetic samples generated by this cohort can boost disease prediction of a different external cohort.

bioinformatics↗

bioRxiv2020

Meta-Signer: Metagenomic Signature Identifier based on Rank Aggregation of Features

BackgroundThe advance of metagenomic studies provides the opportunity to identify microbial taxa that are associated to human diseases. Multiple methods exist for the association analysis. However, the results could be inconsistent, presenting challenges in interpreting the host-microbiome interactions. To address this issue, we introduce Meta-Signer, a novel Metagenomic Signature Identifier tool based on rank aggregation of features identified from multiple machine learning models including Random Forest, Support Vector Machines, LASSO, Multi-Layer Perceptron Neural Networks, and our recently developed Convolutional Neural Network framework (PopPhy-CNN). Meta-Signer generates ranked taxa lists by training individual machine learning models over multiple training partitions and aggregates them into a single ranked list by an optimization procedure to represent the most informative and robust microbial features. Meta-Signer can rank taxa using two input forms of the data: the relative abundances of the original taxa and taxa from the populated taxonomic trees generated from the original taxa. The latter form allows the evaluation of the association of microbial features at different taxonomic levels to the disease, which is attributed to our novel model of PopPhy-CNN. ResultsWe evaluate Mega-Signer on five different human gut-microbiome datasets. We demonstrate that the features derived from Meta-Signer were more informative compared to those obtained from other available feature ranking methods. The highly ranked features are strongly supported by published literature. ConclusionMeta-Signer is capable of deriving a robust set of microbial features at multiple taxonomic levels for the prediction of host phenotype. Meta-Signer is user-friendly and customizable, allowing users to explore their datasets quickly and efficiently.

bioinformatics↗

bioRxiv2018

PopPhy-CNN: A Phylogenetic Tree Embedded Architecture for Convolution Neural Networks for Metagenomic Data

MotivationAccurate prediction of the host phenotype from a metgenomic sample and identification of the associated bacterial markers are important in metagenomic studies. We introduce PopPhy-CNN, a novel convolutional neural networks (CNN) learning architecture that effectively exploits phylogentic structure in microbial taxa. PopPhy-CNN provides an input format of 2D matrix created by embedding the phylogenetic tree that is populated with the relative abundance of microbial taxa in a metagenomic sample. This conversion empowers CNNs to explore the spatial relationship of the taxonomic annotations on the tree and their quantitative characteristics in metagenomic data.\n\nResultsPopPhy-CNN is evaluated using three metagenomic datasets of moderate size. We show the superior performance of PopPhy-CNN compared to random forest, support vector machines, LASSO and a baseline 1D-CNN model constructed with relative abundance microbial feature vectors. In addition, we design a novel scheme of feature extraction from the learned CNN models and demonstrate the improved performance when the extracted features are used to train support vector machines.\n\nConclusionPopPhy-CNN is a novel deep learning framework for the prediction of host phenotype from metagenomic samples. PopPhy-CNN can efficiently train models and does not require excessive amount of data. PopPhy-CNN facilities not only retrieval of informative microbial taxa from the trained CNN models but also visualization of the taxa on the phynogenetic tree.\n\nContactyagndai@uic.edu\n\nAvailabilitySource code is publicly available at https://github.com/derekreiman/PopPhy-CNN\n\nSupplementary informationSupplementary data are available at Bioinformatics online.

bioinformatics↗