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

MicroRNAs01:22

MicroRNAs

3.7K
MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
3.7K
MicroRNAs01:22

MicroRNAs

23.8K
MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After...
23.8K
lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

9.7K
In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
9.7K

You might also read

Related Articles

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

Sort by
Same author

Multimodality imaging in a patient with non-obstructive hypertrophic cardiomyopathy and multivessel coronary artery disease presenting with chest pain: a case report.

BMC cardiovascular disorders·2026
Same author

Lymphedema Care after Breast Cancer Surgery: Insights from a New Meta-Analysis.

Lymphatic research and biology·2026
Same author

GMC-DMA: GNN-Mamba Co-Contrastive Optimization for Disease-Metabolite Association Prediction.

Interdisciplinary sciences, computational life sciences·2026
Same author

Mamba-enhanced disease semantic knowledge graph for interpretable automatic ICD coding.

Journal of biomedical informatics·2025
Same author

Chiroptical isomerization in chiral covalent organic frameworks with identical mesoscopic helicity.

Nature communications·2025
Same author

GADRC: a graph-based approach for drug repositioning with deep residual networks and computational feature-guided undersampling.

Journal of computer-aided molecular design·2025

Related Experiment Video

Updated: Jan 8, 2026

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

Multi-Head Hypergraph Convolution With Feature Enhancement and Latent Representation Learning for miRNA-Disease

Pengli Lu, Zhong Yan, Fentang Gao

    IEEE Transactions on Computational Biology and Bioinformatics
    |December 18, 2025
    PubMed
    Summary

    This study introduces FKAMHV, a novel framework for predicting miRNA-disease associations by integrating Fast Kolmogorov-Arnold Networks and Multi-Head Hypergraph Convolutional Networks to capture complex topological structures, significantly improving accuracy in sparse data scenarios.

    More Related Videos

    Constructing and Visualizing Models using Mime-based Machine-learning Framework
    06:19

    Constructing and Visualizing Models using Mime-based Machine-learning Framework

    Published on: July 22, 2025

    2.2K
    Characterization of Functionally Associated miRNAs in Glioblastoma and their Engineering into Artificial Clusters for Gene Therapy
    09:40

    Characterization of Functionally Associated miRNAs in Glioblastoma and their Engineering into Artificial Clusters for Gene Therapy

    Published on: October 4, 2019

    5.9K

    Related Experiment Videos

    Last Updated: Jan 8, 2026

    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
    Constructing and Visualizing Models using Mime-based Machine-learning Framework
    06:19

    Constructing and Visualizing Models using Mime-based Machine-learning Framework

    Published on: July 22, 2025

    2.2K
    Characterization of Functionally Associated miRNAs in Glioblastoma and their Engineering into Artificial Clusters for Gene Therapy
    09:40

    Characterization of Functionally Associated miRNAs in Glioblastoma and their Engineering into Artificial Clusters for Gene Therapy

    Published on: October 4, 2019

    5.9K

    Area of Science:

    • Bioinformatics
    • Computational Biology
    • Network Medicine

    Background:

    • MicroRNA (miRNA)-disease associations are vital for understanding disease mechanisms.
    • Existing computational methods struggle with sparse data and capturing deep topological structures.

    Purpose of the Study:

    • To develop a novel framework, FKAMHV, for robust miRNA-disease association prediction.
    • To enhance the extraction of deep topological features and uncover latent associations, especially under sparse conditions.

    Main Methods:

    • Constructed heterogeneous networks and generated miRNA/disease-specific hypergraphs.
    • Integrated Fast Kolmogorov-Arnold Networks (FastKAN) for nonlinear feature modeling and Multi-Head Hypergraph Convolutional Networks (Multi-Head HGCN) for joint representation.
    • Employed $\beta$-Variational Autoencoder ($\beta$-VAE) for latent association modeling and introduced attention mechanisms and Jumping Knowledge strategy within HGCN.

    Main Results:

    • FKAMHV demonstrated superior performance over existing methods in terms of Area Under the Curve (AUC) and Area Under the Precision-Recall Curve (AUPR).
    • The framework achieved strong predictive performance even with sparse association data.

    Conclusions:

    • FKAMHV effectively captures complex topological structures and latent associations for miRNA-disease prediction.
    • The proposed method offers improved generalization and robustness, particularly in sparse data settings, advancing the field of computational disease association studies.