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arXiv research

A locally-built, LLM-digested index of recent arXiv papers in quant finance, geometry/topology, and statistical ML — keyword search served straight from SQLite on this machine.

168,657 papers · 148 categories

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56113169225 · Jun 202019922001200920172026
48 results for gene selection

New gene selection method improves tumor classification accuracy.

problem Efficiently selecting relevant genes from high-dimensional tumor gene expression data.
method Fuzzy-Rough Set Theory for feature dependency analysis.
result The proposed method outperforms state-of-the-art techniques in tumor classification.

A novel method selects genes for high-dimensional gene expression data with class imbalance.

problem Class imbalance in gene expression datasets.
method Synthetic data balancing, greedy search, weighted robust score.
result The proposed method outperforms existing feature selection procedures.

Unsupervised method selects genes for tumor subtype discovery.

problem High-dimensional tumor gene expression data with noisy variables and heterogeneity.
method Autoencoders for latent space learning, Multiple Kernel Learning for feature selection, clustering.
result Lower redundancy and better clustering performance compared to benchmarks.

A method selects key genes from tumor transcriptomics data using kernel methods and improves classification performance.

problem Feature selection for tumor classification using gene expression data.
method Multiple Kernel Learning with latent regularization and non-linear dimensionality reduction.
result Improved tumor classification performance on unseen test samples.

New methods detect continuous variation in single-cell data.

problem Continuous variation within and between cell types not detected by discrete analyses.
method Three topologically motivated mathematical methods for unsupervised feature selection.
result Detect additional biologically meaningful genes with coherent expression patterns.

MarkerMap selects key genes for cell type analysis in single-cell RNA-seq.

problem Selecting informative genes from large single-cell RNA-seq datasets is challenging and computationally intensive.
method MarkerMap is a generative model that identifies minimal gene sets explaining cell type variability.
result MarkerMap outperforms existing methods in both supervised and unsupervised marker selection.

Identifying significant subsets of the genes, gene shaving is an essential and challenging issue for biomedical research for a huge number of genes and the complex nature of biological networks,. Since positive definite kernel based methods on genomic information can improve the prediction of diseases, in this paper we…

2018-09-05abs ↗pdf ↗

Study improves cancer classification using gene selection and projection methods.

problem Overfitting in high-dimensional microarray datasets for cancer classification.
method FSWOR technique, random projection, Kendall test, ensemble classifiers, LDA projection, Naïve Bayes.
result Achieved a test score of 96%, significantly outperforming existing methods.

SVB method provides scalable Bayesian proportional hazards model for high-dimensional gene expression data.

problem Bayesian methods for high-dimensional sparse survival data often sacrifice uncertainty quantification or computational scalability.
method Mean-field variational approximation for scalable Bayesian proportional hazards model.
result SVB method offers posterior distribution for parameters and variable selection via posterior inclusion probabilities.

Motivation : Molecular signatures for diagnosis or prognosis estimated from large-scale gene expression data often lack robustness and stability, rendering their biological interpretation challenging. Increasing the signature's interpretability and stability across perturbations of a given dataset and, if possible, acr…

2010-01-18abs ↗pdf ↗

Model learns to select relevant clinical variables for disease subtype prediction from small data.

problem Few-shot disease subtype prediction from small genomic data.
method Meta learning Prototypical Network with feature selection and sample reweighting.
result Superior performance in predicting disease subtypes and identifying genes.

iDeepViewLearn combines deep learning and feature selection for multiview learning.

problem Learning nonlinear relationships in data from multiple complementary views.
method Combines deep learning flexibility with statistical feature selection using deep neural networks and graph Laplacian regularization.
result Identifies genes and CpG sites that differentiate between breast cancer survivors and non-survivors.

BioBO optimizes gene perturbation design using Bayesian optimization with biological priors.

problem Efficient design of genomic perturbation experiments in drug discovery.
method Integrates Bayesian optimization with multimodal gene embeddings and enrichment analysis.
result Improves labeling efficiency by 25-40% and identifies top-performing perturbations more effectively.

Microarray is a technology to quantitatively monitor the expression of large number of genes in parallel. It has become one of the main tools for global gene expression analysis in molecular biology research in recent years. The large amount of expression data generated by this technology makes the study of certain com…

2015-06-05abs ↗pdf ↗

The paper develops a test for independence of selected Gaussian variables after thresholding correlations.

problem Testing independence of selected Gaussian variables after thresholding correlations.
method The approach involves conditioning on the selection event and using a new characterization of the conditioning event in terms of canonical correlation.
result The proposed test has higher power than a naive approach that ignores selection effects.

The linking genotype to phenotype is the fundamental aim of modern genetics. We focus on study of links between gene expression data and phenotype data through integrative analysis. We propose three approaches. 1) The inherent complexity of phenotypes makes high-throughput phenotype profiling a very difficult and labor…

2015-06-29abs ↗pdf ↗

Bayesian methods detect clusters in noisy data more reliably.

problem Noisy data distorts traditional clustering methods, leading to unreliable results.
method Bayesian community detection using Minimum Description Length principle.
result Bayesian methods identify more robust clusters in noisy data.

We consider large-scale studies in which it is of interest to test a very large number of hypotheses, and then to estimate the effect sizes corresponding to the rejected hypotheses. For instance, this setting arises in the analysis of gene expression or DNA sequencing data. However, naive estimates of the effect sizes …

2014-05-16abs ↗pdf ↗

CausalRegNet generates accurate data for gene perturbation experiments, improving CSL methods.

problem Assessing and selecting causal structure learning methods in gene perturbation experiments.
method CausalRegNet, a multiplicative effect structural causal model, generates accurate observational and interventional data.
result CausalRegNet generates more accurate distributions and scales better than current simulation frameworks.

We consider the problem of high-dimensional classification between the two groups with unequal covariance matrices. Rather than estimating the full quadratic discriminant rule, we propose to perform simultaneous variable selection and linear dimension reduction on original data, with the subsequent application of quadr…

2017-11-13abs ↗pdf ↗

Bayesian optimization improves classifier selection for acute infection and mortality.

problem Improving accuracy of acute infection and mortality prediction.
method Comparison of hyperparameter optimization methods (grid search, random sampling, Bayesian optimization).
result Bayesian optimization outperforms grid search or random sampling for in-hospital mortality classifiers.

A new method speeds up overlapping group lasso computations.

problem Time-consuming optimization of overlapping group lasso on large-scale problems.
method Non-overlapping statistical approximation to overlapping group lasso.
result The proposed penalty is statistically equivalent to overlapping group lasso.

We consider a problem of data integration. Consider determining which genes affect a disease. The genes, which we call predictor objects, can be measured in different experiments on the same individual. We address the question of finding which genes are predictors of disease by any of the experiments. Our formulation i…

2016-10-03abs ↗pdf ↗

SPPCSO addresses multicollinearity in high-dimensional data, improving model stability and predictive accuracy.

problem Multicollinearity in high-dimensional data leads to unstable estimation and reduced predictive accuracy.
method SPPCSO integrates principal component regression and L1 regularization to adaptively adjust shrinkage factors.
result SPPCSO achieves stable and reliable estimation in high-noise settings, distinguishing signal variables from noise.