Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

RNA-seq03:21

RNA-seq

11.6K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
11.6K
Cancer Survival Analysis01:21

Cancer Survival Analysis

575
Cancer survival analysis focuses on quantifying and interpreting the time from a key starting point, such as diagnosis or the initiation of treatment, to a specific endpoint, such as remission or death. This analysis provides critical insights into treatment effectiveness and factors that influence patient outcomes, helping to shape clinical decisions and guide prognostic evaluations. A cornerstone of oncology research, survival analysis tackles the challenges of skewed, non-normally...
575

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Replicability of multivariate brain-behaviour associations depends on clinical profile.

Communications biology·2026
Same author

Co-occurring rare germline DNA repair gene variants in BRCA1/BRCA2 implicated hereditary breast cancer families.

NPJ breast cancer·2026
Same author

Nature vs nurture of glucose homeostasis trajectories in children from the ALSPAC study.

Diabetologia·2026
Same author

Development and validation of a trans-ancestry polygenic risk score for type 1 diabetes.

Diabetologia·2026
Same author

KDM5C and KDM5D influence DNA methylation in adult mouse liver.

Biology of sex differences·2026
Same author

The Genetic and Molecular Analyses of Rare Candidate Germline <i>BRIP1/FANCJ</i> Variants Implicated in Hereditary Breast and Ovarian Cancers.

International journal of molecular sciences·2026

Related Experiment Video

Updated: Dec 18, 2025

Selecting Multiple Biomarker Subsets with Similarly Effective Binary Classification Performances
07:35

Selecting Multiple Biomarker Subsets with Similarly Effective Binary Classification Performances

Published on: October 11, 2018

7.9K

Bayesian Hyper-LASSO Classification for Feature Selection with Application to Endometrial Cancer RNA-seq Data.

Lai Jiang1,2, Celia M T Greenwood3,4,5, Weixin Yao6

  • 1Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Canada. lai.jiang@mail.mcgill.ca.

Scientific Reports
|June 18, 2020
PubMed
Summary

BayesHL, a new Bayesian method, effectively selects important genes from high-dimensional genomic data by considering gene expression patterns. It outperforms other methods in predicting cancer survival and uncovering biological pathways.

More Related Videos

Author Spotlight: Impact of Intergenic Interactions on Disease-Identifying Dark Biomarkers
03:37

Author Spotlight: Impact of Intergenic Interactions on Disease-Identifying Dark Biomarkers

Published on: March 1, 2024

1.2K
Machine Learning Algorithms for Early Detection of Bone Metastases in an Experimental Rat Model
07:15

Machine Learning Algorithms for Early Detection of Bone Metastases in an Experimental Rat Model

Published on: August 16, 2020

7.3K

Related Experiment Videos

Last Updated: Dec 18, 2025

Selecting Multiple Biomarker Subsets with Similarly Effective Binary Classification Performances
07:35

Selecting Multiple Biomarker Subsets with Similarly Effective Binary Classification Performances

Published on: October 11, 2018

7.9K
Author Spotlight: Impact of Intergenic Interactions on Disease-Identifying Dark Biomarkers
03:37

Author Spotlight: Impact of Intergenic Interactions on Disease-Identifying Dark Biomarkers

Published on: March 1, 2024

1.2K
Machine Learning Algorithms for Early Detection of Bone Metastases in an Experimental Rat Model
07:15

Machine Learning Algorithms for Early Detection of Bone Metastases in an Experimental Rat Model

Published on: August 16, 2020

7.3K

Area of Science:

  • Genomics
  • Biostatistics
  • Bioinformatics

Background:

  • High-dimensional genomic data analysis is crucial for identifying disease-related gene signatures.
  • Gene expression data often exhibits inherent grouping structures based on biological functions.
  • Existing feature selection methods may not fully leverage these grouping structures.

Purpose of the Study:

  • To propose a novel Bayesian Robit regression method with Hyper-LASSO priors (BayesHL) for feature selection in high-dimensional genomic data.
  • To develop a method that automatically handles grouping structures without pre-specification.
  • To identify gene signatures associated with endometrial cancer survival.

Main Methods:

  • Bayesian Robit regression with Hyper-LASSO priors (BayesHL).
  • Application to high-dimensional gene expression data with inherent grouping.
  • Comparison with established methods like LASSO, group LASSO, and machine learning algorithms.

Main Results:

  • BayesHL demonstrates superior predictive power and sparsity compared to alternative methods.
  • The method effectively identifies gene subsets contributing to endometrial cancer survival.
  • BayesHL successfully uncovers grouping structures and provides insights into genetic pathways.

Conclusions:

  • BayesHL is a powerful tool for feature selection in high-dimensional genomic data, especially when grouping structures are present.
  • The method offers advantages in predictive accuracy, feature sparsity, and biological interpretability.
  • Findings contribute to understanding the genetic mechanisms underlying endometrial cancer survival.