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

lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

8.8K
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...
8.8K
Factors Affecting Illness01:18

Factors Affecting Illness

4.3K
When a person's physical, emotional, intellectual, social development or spiritual functioning is compromised, this deviation from a healthy normal state is called illness. Illness creates stress that in turn harms individuals. Irritation, anger, denial, hopelessness, and fear are behavioral and emotional changes an individual experiences in the phases of illness. A variety of factors influence a person's health and well-being.
For instance, risk factors are connected to illness,...
4.3K
Calculating and Interpreting the Linear Correlation Coefficient01:11

Calculating and Interpreting the Linear Correlation Coefficient

6.4K
The correlation coefficient, r, developed by Karl Pearson in the early 1900s, is numerical and provides a measure of strength and direction of the linear association between the independent variable, x, and the dependent variable, y. Hence, it is also known as the Pearson product-moment correlation coefficient. It can be calculated using the following equation:
6.4K
Improving Translational Accuracy02:07

Improving Translational Accuracy

11.8K
Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
11.8K
Cancer Survival Analysis01:21

Cancer Survival Analysis

423
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...
423
Correlation and Regression00:53

Correlation and Regression

1.4K
In statistics, correlation describes the degree of association between two variables. In the subfield of linear regression, correlation is mathematically expressed by the correlation coefficient, which describes the strength and direction of the relationship between two variables. The coefficient is symbolically represented by 'r' and ranges from -1 to +1. A positive value indicates a positive correlation where the two variables move in the same direction. A negative value suggests a...
1.4K

You might also read

Related Articles

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

Sort by
Same author

Exploring Complex Genetic Mechanisms in Brain Imaging Genetics via a New Multi-task Learning Method.

IEEE transactions on computational biology and bioinformatics·2026
Same author

stDGCN: A dual-augmentation graph convolutional network for identifying spatial domains with attention mechanism.

IEEE journal of biomedical and health informatics·2026
Same author

MVCL: A Contrastive Learning Model with Multi-view Networks for Driver Gene Prediction.

IEEE journal of biomedical and health informatics·2026
Same author

scDEBGCL: a deep embedding approach based on bipartite graph contrastive learning for single-cell RNA-seq data.

BMC biology·2026
Same author

scSCCNIA: similarity matrix based contrastive clustering with neighbor information aggregation for single-cell RNA sequencing data.

Briefings in bioinformatics·2026
Same author

DeepSGE: predicting spatial gene expression using residual network with efficient channel attention and dynamic graph attention network.

BMC genomics·2026

Related Experiment Video

Updated: Aug 25, 2025

Analyzing Tumor Gene Expression Factors with the CorExplorer Web Portal
08:00

Analyzing Tumor Gene Expression Factors with the CorExplorer Web Portal

Published on: October 11, 2019

7.6K

LDCMFC: Predicting Long Non-Coding RNA and Disease Association Using Collaborative Matrix Factorization Based on

Wen-Yu Xi, Feng Zhou, Ying-Lian Gao

    IEEE/ACM Transactions on Computational Biology and Bioinformatics
    |October 17, 2022
    PubMed
    Summary
    This summary is machine-generated.

    A new method, LDCMFC, accurately predicts long non-coding RNA-disease associations (LDAs) using correntropy and WKNKN. This approach offers a feasible and effective way to identify potential LDAs for intractable diseases.

    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

    857
    Author Spotlight: Integrated Multi-Omics Analysis for Unveiling Multicellular Immune Signatures in Clinical Heart Attack Cohorts
    08:51

    Author Spotlight: Integrated Multi-Omics Analysis for Unveiling Multicellular Immune Signatures in Clinical Heart Attack Cohorts

    Published on: September 20, 2024

    1.4K

    Related Experiment Videos

    Last Updated: Aug 25, 2025

    Analyzing Tumor Gene Expression Factors with the CorExplorer Web Portal
    08:00

    Analyzing Tumor Gene Expression Factors with the CorExplorer Web Portal

    Published on: October 11, 2019

    7.6K
    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

    857
    Author Spotlight: Integrated Multi-Omics Analysis for Unveiling Multicellular Immune Signatures in Clinical Heart Attack Cohorts
    08:51

    Author Spotlight: Integrated Multi-Omics Analysis for Unveiling Multicellular Immune Signatures in Clinical Heart Attack Cohorts

    Published on: September 20, 2024

    1.4K

    Area of Science:

    • Bioinformatics and computational biology
    • Genomics and molecular biology
    • Disease association studies

    Background:

    • Long non-coding RNAs (lncRNAs) play a crucial role in various intractable diseases.
    • Identifying lncRNA-disease associations (LDAs) is challenging and expensive, limiting current knowledge.
    • Accurate and efficient methods are vital for discovering novel LDAs.

    Purpose of the Study:

    • To propose a novel computational method for identifying potential lncRNA-disease associations (LDAs).
    • To enhance the robustness and accuracy of LDA prediction algorithms.
    • To provide a feasible tool for exploring unknown LDAs.

    Main Methods:

    • Developed a collaborative matrix factorization method based on correntropy (LDCMFC).
    • Replaced Euclidean distance minimization with correntropy maximization for improved robustness.
    • Utilized the weighted K nearest known neighbor (WKNKN) method to reconstruct the adjacency matrix.

    Main Results:

    • LDCMFC achieved a high Area Under the Curve (AUC) of 0.8628 in 5-fold cross-validation.
    • The method demonstrated superior performance compared to traditional LDA prediction techniques.
    • Experimental validation in three cancer types confirmed the accuracy of predicted lncRNAs.

    Conclusions:

    • LDCMFC is a feasible and effective computational method for predicting lncRNA-disease associations.
    • The proposed approach offers a robust and accurate alternative for LDA discovery.
    • This method can aid in understanding the role of lncRNAs in intractable diseases.