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

You might also read

Related Articles

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

Sort by
Same author

The role of PN-like junction effects in energy storage performances for Ag<sub>2</sub>O nanoparticle dispersed lead-free K<sub>0.5</sub>Na<sub>0.5</sub>NbO<sub>3</sub>-BiMnO<sub>3</sub> films.

Nanoscale·2020
Same author

Pro-515 of the dynamin-like GTPase MxB contributes to HIV-1 inhibition by regulating MxB oligomerization and binding to HIV-1 capsid.

The Journal of biological chemistry·2020
Same author

Efficient solar hydrogen production coupled with organics degradation by a hybrid tandem photocatalytic fuel cell using a silicon-doped TiO<sub>2</sub> nanorod array with enhanced electronic properties.

Journal of hazardous materials·2020
Same author

Ribitol enhances matriglycan of α-dystroglycan in breast cancer cells without affecting cell growth.

Scientific reports·2020
Same author

RUNX3 Inhibits the Invasion and Metastasis of Human Colon Cancer HT-29 Cells by Upregulating MMP-2/9.

Evidence-based complementary and alternative medicine : eCAM·2020
Same author

Observation of changes in the number of myocardial capillaries in rabbits after treatment of acute myocardial infarction by Tongxinluo superfine powder.

Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan·2020

Related Experiment Video

Updated: Mar 3, 2026

A Method for Measuring RNA N6-methyladenosine Modifications in Cells and Tissues
08:56

A Method for Measuring RNA N6-methyladenosine Modifications in Cells and Tissues

Published on: December 5, 2016

11.4K

Identifying N6-methyladenosine sites using multi-interval nucleotide pair position specificity and support vector

Pengwei Xing1, Ran Su2, Fei Guo1

  • 1School of Computer Science and Technology, Tianjin University, Tianjin, China.

Scientific Reports
|April 26, 2017
PubMed
Summary

A new computational tool, RAM-NPPS, accurately identifies N6-methyladenosine (m6A) sites in RNA sequences. This method offers a faster, cost-effective alternative to experimental techniques for understanding m6A functions.

More Related Videos

Specificity Analysis of Protein Lysine Methyltransferases Using SPOT Peptide Arrays
08:48

Specificity Analysis of Protein Lysine Methyltransferases Using SPOT Peptide Arrays

Published on: November 29, 2014

14.5K
Exploring m6A and m5C Epitranscriptomes upon Viral Infection: an Example with HIV
14:40

Exploring m6A and m5C Epitranscriptomes upon Viral Infection: an Example with HIV

Published on: March 5, 2022

3.8K

Related Experiment Videos

Last Updated: Mar 3, 2026

A Method for Measuring RNA N6-methyladenosine Modifications in Cells and Tissues
08:56

A Method for Measuring RNA N6-methyladenosine Modifications in Cells and Tissues

Published on: December 5, 2016

11.4K
Specificity Analysis of Protein Lysine Methyltransferases Using SPOT Peptide Arrays
08:48

Specificity Analysis of Protein Lysine Methyltransferases Using SPOT Peptide Arrays

Published on: November 29, 2014

14.5K
Exploring m6A and m5C Epitranscriptomes upon Viral Infection: an Example with HIV
14:40

Exploring m6A and m5C Epitranscriptomes upon Viral Infection: an Example with HIV

Published on: March 5, 2022

3.8K

Area of Science:

  • Molecular Biology
  • Bioinformatics
  • Genomics

Background:

  • N6-methyladenosine (m6A) is a crucial RNA modification involved in various biological processes including splicing, mRNA export, and translation.
  • Experimental identification of m6A sites is essential but becomes time-consuming and costly with the rapid expansion of genomic data.

Purpose of the Study:

  • To develop a fast and accurate computational method for identifying m6A sites in RNA sequences.
  • To introduce a novel sequence-based predictor, RAM-NPPS, to address the limitations of experimental m6A site identification.

Main Methods:

  • Proposed a novel feature representation algorithm based on multi-interval nucleotide pair position specificity.
  • Utilized a support vector machine classifier to build the prediction model for m6A sites.
  • Developed RAM-NPPS, a sequence-based predictor for m6A site identification.

Main Results:

  • The RAM-NPPS predictor demonstrated superior performance compared to existing state-of-the-art methods.
  • The method showed effectiveness and robustness across three benchmark datasets and three species.
  • An online webserver for RAM-NPPS was established for public use.

Conclusions:

  • RAM-NPPS provides an efficient and reliable computational tool for identifying m6A sites.
  • The predictor can significantly assist researchers in exploring the functional mechanisms of m6A.
  • This work highlights the potential of computational approaches in advancing RNA epigenetics research.