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Elliott Gordon-Rodríguez

dblp:259/3205 · DBLP profile ↗
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3ranked-venue papers
3as first author
2since 2021 · last 2022
0000-0002-2720-1756ORCID · verified

Domains — the database's venue-derived domains; a paper can count in several

Artificial intelligence and machine learning · 2 · 2 first-author · 1 since 2021Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
2 papers
Bioinformatics and computational biology · 81% Computational science and engineering · 19%
Artificial intelligence
2 papers
Probabilistic and Bayesian machine learning · 60% Representation and self-supervised learning · 40%

Topics — the 8 heaviest of 9, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Machine learning › Representation and self-supervised learning
contrastive learning
0.612022
Data Augmentation for Compositional Data: Advancing Predictive Models of the Microbiome · NeurIPS 2022
Bioinformatics and computational biology › computational microbiology
microbiome analysis
0.612022
Data Augmentation for Compositional Data: Advancing Predictive Models of the Microbiome · NeurIPS 2022
Bioinformatics and computational biology › computational microbiology › microbiome analysis
microbiome disease prediction
0.612022
Data Augmentation for Compositional Data: Advancing Predictive Models of the Microbiome · NeurIPS 2022
Bioinformatics and computational biology
biomarker discovery
0.512021
Learning sparse log-ratios for high-throughput sequencing data · Bioinform. 2021
Computational science and engineering
compositional data analysis
0.512021
Learning sparse log-ratios for high-throughput sequencing data · Bioinform. 2021
Bioinformatics and computational biology › genomics
high-throughput sequencing data
0.512021
Learning sparse log-ratios for high-throughput sequencing data · Bioinform. 2021
Machine learning › Probabilistic and Bayesian machine learning › statistical inference
exponential family
0.412020
The continuous categorical: a novel simplex-valued exponential family · ICML 2020
Machine learning › Probabilistic and Bayesian machine learning
reparameterization trick
0.412020
The continuous categorical: a novel simplex-valued exponential family · ICML 2020

Methods — techniques the papers use, named apart from their topics

sub-composition · 1.1contrastive learning · 1.1aitchison geometry · 1.1gradient descent · 0.5deep learning · 0.5continuous relaxation · 0.5sampling · 0.4reparameterization trick · 0.4exponential family · 0.4
YearPublicationVenuePosition
2022 Data Augmentation for Compositional Data: Advancing Predictive Models of the Microbiome
abstract
Data augmentation plays a key role in modern machine learning pipelines. While numerous augmentation strategies have been studied in the context of computer vision and natural language processing, less is known for other data modalities. Our work extends the success of data augmentation to compositional data, i.e., simplex-valued data, which is of particular interest in microbiology, geochemistry, and other applications. Drawing on key principles from compositional data analysis, such as the \emph{Aitchison geometry of the simplex} and subcompositions, we define novel augmentation strategies for this data modality. Incorporating our data augmentations into standard supervised learning pipelines results in consistent performance gains across a wide range of standard benchmark datasets. In particular, we set a new state-of-the-art for key disease prediction tasks including colorectal cancer, type 2 diabetes, and Crohn's disease. In addition, our data augmentations enable us to define a novel contrastive learning model, which improves on previous representation learning approaches for microbiome compositional data.
Elliott Gordon-Rodríguez, Thomas P. Quinn, John P. Cunningham
NeurIPS1
2021 Learning sparse log-ratios for high-throughput sequencing data
abstract
MOTIVATION: The automatic discovery of sparse biomarkers that are associated with an outcome of interest is a central goal of bioinformatics. In the context of high-throughput sequencing (HTS) data, and compositional data (CoDa) more generally, an important class of biomarkers are the log-ratios between the input variables. However, identifying predictive log-ratio biomarkers from HTS data is a combinatorial optimization problem, which is computationally challenging. Existing methods are slow to run and scale poorly with the dimension of the input, which has limited their application to low- and moderate-dimensional metagenomic datasets. RESULTS: Building on recent advances from the field of deep learning, we present CoDaCoRe, a novel learning algorithm that identifies sparse, interpretable and predictive log-ratio biomarkers. Our algorithm exploits a continuous relaxation to approximate the underlying combinatorial optimization problem. This relaxation can then be optimized efficiently using the modern ML toolbox, in particular, gradient descent. As a result, CoDaCoRe runs several orders of magnitude faster than competing methods, all while achieving state-of-the-art performance in terms of predictive accuracy and sparsity. We verify the outperformance of CoDaCoRe across a wide range of microbiome, metabolite and microRNA benchmark datasets, as well as a particularly high-dimensional dataset that is outright computationally intractable for existing sparse log-ratio selection methods. AVAILABILITY AND IMPLEMENTATION: The CoDaCoRe package is available at https://github.com/egr95/R-codacore. Code and instructions for reproducing our results are available at https://github.com/cunningham-lab/codacore. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Elliott Gordon-Rodríguez, Thomas P. Quinn, John P. Cunningham
Bioinform.1
2020 The continuous categorical: a novel simplex-valued exponential family
abstract
Simplex-valued data appear throughout statistics and machine learning, for example in the context of transfer learning and compression of deep networks. Existing models for this class of data rely on the Dirichlet distribution or other related loss functions; here we show these standard choices suffer systematically from a number of limitations, including bias and numerical issues that frustrate the use of flexible network models upstream of these distributions. We resolve these limitations by introducing a novel exponential family of distributions for modeling simplex-valued data {–} the continuous categorical, which arises as a nontrivial multivariate generalization of the recently discovered continuous Bernoulli. Unlike the Dirichlet and other typical choices, the continuous categorical results in a well-behaved probabilistic loss function that produces unbiased estimators, while preserving the mathematical simplicity of the Dirichlet. As well as exploring its theoretical properties, we introduce sampling methods for this distribution that are amenable to the reparameterization trick, and evaluate their performance. Lastly, we demonstrate that the continuous categorical outperforms standard choices empirically, across a simulation study, an applied example on multi-party elections, and a neural network compression task.
Elliott Gordon-Rodríguez, Gabriel Loaiza-Ganem, John P. Cunningham
ICML1