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

Cis-regulatory Sequences02:02

Cis-regulatory Sequences

3.7K
3.7K
Cis-regulatory Sequences02:02

Cis-regulatory Sequences

11.3K
Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
11.3K
Conserved Binding Sites01:49

Conserved Binding Sites

4.9K
Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...
4.9K

You might also read

Related Articles

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

Sort by
Same author

CryoSIP: unleashing protein high-resolution Cryo-EM via semantic-instance collaborative picking.

Briefings in bioinformatics·2026
Same author

A deep adversarial network model for multi-task analysis of single-cell omics data.

Briefings in bioinformatics·2026
Same author

ST-GCP: a graph convolutional network model with contrastive consistency and permutation for spatial transcriptomics.

Briefings in bioinformatics·2025
Same author

GRAPE: graph-regularized protein language modeling unlocks TCR-epitope binding specificity.

Briefings in bioinformatics·2025
Same author

GraphADT: empowering interpretable predictions of acute dermal toxicity with multi-view graph pooling and structure remapping.

Bioinformatics (Oxford, England)·2024
Same author

Revisiting drug-protein interaction prediction: a novel global-local perspective.

Bioinformatics (Oxford, England)·2024
Same journal

Cross-Domain Transfer Learning from Peptides to Metabolites Using a Multi-Property Fine-Tuned LLM.

Bioinformatics (Oxford, England)·2026
Same journal

Biomedical Concept Recognition with Error-aware Negative-enhanced Ranking Framework.

Bioinformatics (Oxford, England)·2026
Same journal

TEDLH: Domain HMMs for sensitive detection of remote homologues.

Bioinformatics (Oxford, England)·2026
Same journal

PLNFGL: Joint Estimation of Multi-Condition Gene Networks from Single-cell RNA-seq Data.

Bioinformatics (Oxford, England)·2026
Same journal

MCFST: Spatial domain identification method based on multi-view graph convolutional network and graph fusion network.

Bioinformatics (Oxford, England)·2026
Same journal

SpaBiT: Enhancing Spatial Transcriptomics Resolution via Bidirectional Attention Transformers.

Bioinformatics (Oxford, England)·2026
See all related articles

Related Experiment Video

Updated: Dec 3, 2025

A Web-Based Workflow for Selecting Gene- and Tissue-Specific Enhancers
08:12

A Web-Based Workflow for Selecting Gene- and Tissue-Specific Enhancers

Published on: July 18, 2025

464

iEnhancer-XG: interpretable sequence-based enhancers and their strength predictor.

Lijun Cai1, Xuanbai Ren1, Xiangzheng Fu1

  • 1College of Computer Science and Electronic Engineering, Hunan University, 410082 Changsha, Hunan, China.

Bioinformatics (Oxford, England)
|October 29, 2020
PubMed
Summary
This summary is machine-generated.

We developed iEnhancer-XG, a novel two-layer predictor for identifying enhancers and their strengths. This machine learning tool significantly improves accuracy over existing methods for gene expression control.

More Related Videos

A Computational Pipeline for Intergenic/Intragenic Enhancer RNA Quantification in Mouse Embryonic Stem Cells
06:02

A Computational Pipeline for Intergenic/Intragenic Enhancer RNA Quantification in Mouse Embryonic Stem Cells

Published on: October 28, 2025

181
Dissection of Enhancer Function Using Multiplex CRISPR-based Enhancer Interference in Cell Lines
10:46

Dissection of Enhancer Function Using Multiplex CRISPR-based Enhancer Interference in Cell Lines

Published on: June 2, 2018

9.6K

Related Experiment Videos

Last Updated: Dec 3, 2025

A Web-Based Workflow for Selecting Gene- and Tissue-Specific Enhancers
08:12

A Web-Based Workflow for Selecting Gene- and Tissue-Specific Enhancers

Published on: July 18, 2025

464
A Computational Pipeline for Intergenic/Intragenic Enhancer RNA Quantification in Mouse Embryonic Stem Cells
06:02

A Computational Pipeline for Intergenic/Intragenic Enhancer RNA Quantification in Mouse Embryonic Stem Cells

Published on: October 28, 2025

181
Dissection of Enhancer Function Using Multiplex CRISPR-based Enhancer Interference in Cell Lines
10:46

Dissection of Enhancer Function Using Multiplex CRISPR-based Enhancer Interference in Cell Lines

Published on: June 2, 2018

9.6K

Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Enhancers are crucial non-coding DNA elements regulating gene expression.
  • Current machine learning tools for enhancer identification have limitations in accuracy and efficiency.

Purpose of the Study:

  • To develop an accurate and efficient predictor for identifying enhancers and their strengths.
  • To improve the interpretability and credibility of machine learning models in genomics.

Main Methods:

  • Proposed a two-layer predictor, iEnhancer-XG, utilizing XGBoost as the base classifier.
  • Employed five feature extraction methods: k-Spectrum Profile, Mismatch k-tuple, Subsequence Profile, PSSM, and PseDNC.
  • Integrated an ensemble learning approach for feature fusion and SHapley Additive explanations for model interpretability.

Main Results:

  • Achieved prediction accuracies of 0.811 for enhancer identification (first layer) and 0.657 for strength prediction (second layer).
  • Demonstrated superior performance compared to existing technologies through rigorous 10-fold cross-validation.

Conclusions:

  • iEnhancer-XG offers a significant advancement in enhancer prediction accuracy and efficiency.
  • The ensemble learning approach and interpretability methods enhance the reliability of computational predictions in genomics.