Data-Driven Logistic Regression Ensembles With Applications in Genomics
- URL: http://arxiv.org/abs/2102.08591v5
- Date: Thu, 21 Nov 2024 05:52:27 GMT
- Title: Data-Driven Logistic Regression Ensembles With Applications in Genomics
- Authors: Anthony-Alexander Christidis, Stefan Van Aelst, Ruben Zamar,
- Abstract summary: We propose a new approach for dealing with high-dimensional binary classification problems that combines ideas from regularization and ensembling.
We demonstrate the good performance of our method in terms of prediction accuracy and identification of key biomarkers using several medical datasets involving common diseases such as cancer, multiple sclerosis and psoriasis.
- Score: 0.0
- License:
- Abstract: Advances in data collecting technologies in genomics have significantly increased the need for tools designed to study the genetic basis of many diseases. Statistical tools used to discover patterns between the expression of certain genes and the presence of diseases should ideally perform well in terms of both prediction accuracy and identification of key biomarkers. We propose a new approach for dealing with high-dimensional binary classification problems that combines ideas from regularization and ensembling. The ensembles are comprised of a relatively small number of highly accurate and interpretable models that are learned directly from the data by minimizing a global objective function. We derive the asymptotic properties of our method and develop an efficient algorithm to compute the ensembles. We demonstrate the good performance of our method in terms of prediction accuracy and identification of key biomarkers using several medical genomics datasets involving common diseases such as cancer, multiple sclerosis and psoriasis. In several applications our method could identify key biomarkers that were absent in state-of-the-art competitor methods. We develop a variable importance ranking tool that may guide the focus of researchers on the most promising genes. Based on numerical experiments we provide guidelines for the choice of the number of models in our ensembles.
Related papers
- Stacked ensemble\-based mutagenicity prediction model using multiple modalities with graph attention network [0.9736758288065405]
Mutagenicity is a concern due to its association with genetic mutations which can result in a variety of negative consequences.
In this work, we introduce a novel stacked ensemble based mutagenicity prediction model.
arXiv Detail & Related papers (2024-09-03T09:14:21Z) - Simplicity within biological complexity [0.0]
We survey the literature and argue for the development of a comprehensive framework for embedding of multi-scale molecular network data.
Network embedding methods map nodes to points in low-dimensional space, so that proximity in the learned space reflects the network's topology-function relationships.
We propose to develop a general, comprehensive embedding framework for multi-omic network data, from models to efficient and scalable software implementation.
arXiv Detail & Related papers (2024-05-15T13:32:45Z) - Seeing Unseen: Discover Novel Biomedical Concepts via
Geometry-Constrained Probabilistic Modeling [53.7117640028211]
We present a geometry-constrained probabilistic modeling treatment to resolve the identified issues.
We incorporate a suite of critical geometric properties to impose proper constraints on the layout of constructed embedding space.
A spectral graph-theoretic method is devised to estimate the number of potential novel classes.
arXiv Detail & Related papers (2024-03-02T00:56:05Z) - Single-Cell Deep Clustering Method Assisted by Exogenous Gene
Information: A Novel Approach to Identifying Cell Types [50.55583697209676]
We develop an attention-enhanced graph autoencoder, which is designed to efficiently capture the topological features between cells.
During the clustering process, we integrated both sets of information and reconstructed the features of both cells and genes to generate a discriminative representation.
This research offers enhanced insights into the characteristics and distribution of cells, thereby laying the groundwork for early diagnosis and treatment of diseases.
arXiv Detail & Related papers (2023-11-28T09:14:55Z) - Causal machine learning for single-cell genomics [94.28105176231739]
We discuss the application of machine learning techniques to single-cell genomics and their challenges.
We first present the model that underlies most of current causal approaches to single-cell biology.
We then identify open problems in the application of causal approaches to single-cell data.
arXiv Detail & Related papers (2023-10-23T13:35:24Z) - Embracing assay heterogeneity with neural processes for markedly
improved bioactivity predictions [0.276240219662896]
Predicting the bioactivity of a ligand is one of the hardest and most important challenges in computer-aided drug discovery.
Despite years of data collection and curation efforts, bioactivity data remains sparse and heterogeneous.
We present a hierarchical meta-learning framework that exploits the information synergy across disparate assays.
arXiv Detail & Related papers (2023-08-17T16:26:58Z) - Functional Integrative Bayesian Analysis of High-dimensional
Multiplatform Genomic Data [0.8029049649310213]
We propose a framework called Functional Integrative Bayesian Analysis of High-dimensional Multiplatform Genomic Data (fiBAG)
fiBAG allows simultaneous identification of upstream functional evidence of proteogenomic biomarkers.
We demonstrate the profitability of fiBAG via a pan-cancer analysis of 14 cancer types.
arXiv Detail & Related papers (2022-12-29T03:31:45Z) - Cancer Gene Profiling through Unsupervised Discovery [49.28556294619424]
We introduce a novel, automatic and unsupervised framework to discover low-dimensional gene biomarkers.
Our method is based on the LP-Stability algorithm, a high dimensional center-based unsupervised clustering algorithm.
Our signature reports promising results on distinguishing immune inflammatory and immune desert tumors.
arXiv Detail & Related papers (2021-02-11T09:04:45Z) - G-MIND: An End-to-End Multimodal Imaging-Genetics Framework for
Biomarker Identification and Disease Classification [49.53651166356737]
We propose a novel deep neural network architecture to integrate imaging and genetics data, as guided by diagnosis, that provides interpretable biomarkers.
We have evaluated our model on a population study of schizophrenia that includes two functional MRI (fMRI) paradigms and Single Nucleotide Polymorphism (SNP) data.
arXiv Detail & Related papers (2021-01-27T19:28:04Z) - Select-ProtoNet: Learning to Select for Few-Shot Disease Subtype
Prediction [55.94378672172967]
We focus on few-shot disease subtype prediction problem, identifying subgroups of similar patients.
We introduce meta learning techniques to develop a new model, which can extract the common experience or knowledge from interrelated clinical tasks.
Our new model is built upon a carefully designed meta-learner, called Prototypical Network, that is a simple yet effective meta learning machine for few-shot image classification.
arXiv Detail & Related papers (2020-09-02T02:50:30Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.