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

10.4K
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...
10.4K
RNA Editing02:23

RNA Editing

9.2K
RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
9.2K

You might also read

Related Articles

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

Sort by
Same author

Sex-specific regulation of angiogenin in Alzheimer's disease.

Molecular psychiatry·2026
Same author

ModiCal: A Targeted Calibration Workflow for Site-Specific m<sup>5</sup>C Validation by Nanopore Direct RNA Sequencing.

ACS chemical biology·2026
Same author

Real-time transcriptomic profiling in distinct experimental conditions.

eLife·2026
Same author

A Translational Neural Network Mechanism of Resilience: Top-Down Control and Plasticity of the Visual Cortex Relates to Resilient Outcome and Performance.

Research (Washington, D.C.)·2026
Same author

Mapping human pre-rRNA processing and modification at single nucleotide resolution using long read nanopore sequencing.

Nature communications·2026
Same author

Novel polymer series for pharmaceutical applications: alpha-hydroxycarboxylic acid modified polymethacrylates.

International journal of pharmaceutics·2026
Same journal

Correction to 'New origin firing is inhibited by APC/CCdh1 activation in S-phase after severe replication stress'.

Nucleic acids research·2026
Same journal

VeloRM: disentangling pre- and post-splicing RNA modification dynamics at single-cell resolution.

Nucleic acids research·2026
Same journal

Accessibility of telomeric overhangs to stabilizing small-molecule ligands.

Nucleic acids research·2026
Same journal

Multivalent interactions mediate SNAIL transcription factor stimulation of the nucleosome deacetylase activity of the CoREST complex.

Nucleic acids research·2026
Same journal

Genome-wide mapping of DNA G-quadruplexes in Trypanosoma brucei chromatin reveals enrichment in coding regions and transcription start sites.

Nucleic acids research·2026
Same journal

Correction to 'The Gene Ontology knowledgebase in 2026'.

Nucleic acids research·2026
See all related articles

Related Experiment Video

Updated: Sep 14, 2025

Author Spotlight: Decoding RNA Methylation's Role in Pancreatic Cancer - A Single-Base Resolution Study
06:57

Author Spotlight: Decoding RNA Methylation's Role in Pancreatic Cancer - A Single-Base Resolution Study

Published on: July 7, 2023

1.2K

ModiDeC: a multi-RNA modification classifier for direct nanopore sequencing.

Nicolò Alagna1, Stefan Mündnich2, Johannes Miedema1

  • 1Institute of Human Genetics, University Medical Center Mainz, Mainz 55128, Germany.

Nucleic Acids Research
|July 19, 2025
PubMed
Summary
This summary is machine-generated.

ModiDeC, a new deep-learning tool, accurately identifies multiple RNA modifications using direct RNA sequencing. This advance aids epitranscriptome analysis in various biological samples.

More Related Videos

Sequencing of mRNA from Whole Blood using Nanopore Sequencing
11:26

Sequencing of mRNA from Whole Blood using Nanopore Sequencing

Published on: June 3, 2019

13.9K
2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications
05:41

2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications

Published on: July 10, 2020

2.0K

Related Experiment Videos

Last Updated: Sep 14, 2025

Author Spotlight: Decoding RNA Methylation's Role in Pancreatic Cancer - A Single-Base Resolution Study
06:57

Author Spotlight: Decoding RNA Methylation's Role in Pancreatic Cancer - A Single-Base Resolution Study

Published on: July 7, 2023

1.2K
Sequencing of mRNA from Whole Blood using Nanopore Sequencing
11:26

Sequencing of mRNA from Whole Blood using Nanopore Sequencing

Published on: June 3, 2019

13.9K
2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications
05:41

2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications

Published on: July 10, 2020

2.0K

Area of Science:

  • Molecular Biology
  • Bioinformatics
  • Genomics

Background:

  • RNA modifications are vital for cellular functions.
  • Accurate detection of RNA modifications is crucial for understanding gene regulation.
  • Existing methods may have limitations in identifying multiple modification types simultaneously.

Purpose of the Study:

  • To develop a deep-learning classifier, ModiDeC, for identifying and distinguishing multiple RNA modifications.
  • To create an extensive database of RNA sequences for training and validation.
  • To provide a user-friendly tool for epitranscriptome analysis.

Main Methods:

  • Development of a deep-learning model (ModiDeC) for RNA modification classification.
  • Generation of in vitro-transcribed and synthetic RNA sequences using RNA004 and RNA002 chemistries.
  • Validation of ModiDeC using synthetic data, HEK293T cells, and human blood samples.

Main Results:

  • ModiDeC accurately identifies and distinguishes five types of RNA modifications: N6-methyladenosine, inosine, pseudouridine, 2'-O-methylguanosine, and N1-methyladenosine.
  • High accuracy was observed across different sequence motifs and in various biological samples.
  • The tool demonstrated reproducibility and a low false-positive rate.

Conclusions:

  • ModiDeC is a powerful and adaptable tool for analyzing the epitranscriptome.
  • The graphical user interface and Epi2ME pipeline facilitate customization for specific research needs.
  • ModiDeC advances the field of RNA modification analysis.