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

Improving Translational Accuracy02:07

Improving Translational Accuracy

3.4K
3.4K
Improving Translational Accuracy02:07

Improving Translational Accuracy

13.3K
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...
13.3K
lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

3.2K
3.2K
Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

4.1K
4.1K
Regulated mRNA Transport02:22

Regulated mRNA Transport

3.2K
3.2K
Telomeres and Telomerase02:41

Telomeres and Telomerase

6.6K
6.6K

You might also read

Related Articles

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

Sort by
Same author

Adverse and adaptive placental DNA methylation changes linking prenatal air pollution exposure to child lung function: findings from the SEPAGES cohort.

EBioMedicine·2026
Same author

SeqManager: a web-based tool for efficient sequencing data storage management and duplicate detection.

Bioinformatics advances·2025
Same author

Immediate and durable effects of maternal tobacco consumption on placental DNA methylation: a replication and discovery study.

Environmental epigenetics·2025
Same author

Generating realistic artificial human genomes using adversarial autoencoders.

NAR genomics and bioinformatics·2025
Same author

Monocyte-Derived Macrophages-Synovial Fibroblasts Crosstalk Unravels Oncostatin Signaling Network as a Driver of Synovitis in Osteoarthritis.

Arthritis & rheumatology (Hoboken, N.J.)·2025
Same author

[Environmental exposures and epigenome changes within the first 1000 days of life].

Medecine sciences : M/S·2024
Same journal

conMItion: an R package adjusting confounding factors for associations in multi-omics.

Bioinformatics (Oxford, England)·2026
Same journal

SpaMFG: a Spatial Multi-omics Integration Method based on Feature Grouping.

Bioinformatics (Oxford, England)·2026
Same journal

CSCN: Inference of Cell-Specific Causal Networks Using Single-Cell RNA-Seq Data.

Bioinformatics (Oxford, England)·2026
Same journal

Sparse CCA-Based Mediation Analysis with High-Dimensional Exposures and Mediators.

Bioinformatics (Oxford, England)·2026
Same journal

Enhancing Cross-Context Generalization in Drug Perturbation Prediction with a Multimodal Conditional Diffusion Framework.

Bioinformatics (Oxford, England)·2026
Same journal

Primer Design through Submodular Function Estimation.

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

Related Experiment Video

Updated: Dec 9, 2025

Genome-wide Surveillance of Transcription Errors in Eukaryotic Organisms
09:30

Genome-wide Surveillance of Transcription Errors in Eukaryotic Organisms

Published on: September 13, 2018

9.8K

TALC: Transcript-level Aware Long-read Correction.

Lucile Broseus1, Aubin Thomas1, Andrew J Oldfield1

  • 1Department of Genome Dynamics, Institut de Génétique Humaine, Centre National de la Recherche Scientifique (CNRS), Université de Montpellier, Montpellier 34396, France.

Bioinformatics (Oxford, England)
|September 10, 2020
PubMed
Summary
This summary is machine-generated.

We developed Transcript-level Aware Long-Read Correction (TALC), a novel algorithm to accurately correct errors in long-read RNA sequencing data. TALC improves downstream RNA-seq analysis, making it essential for transcriptome studies using long-read technology.

More Related Videos

Identification of Key Factors Regulating Self-renewal and Differentiation in EML Hematopoietic Precursor Cells by RNA-sequencing Analysis
12:44

Identification of Key Factors Regulating Self-renewal and Differentiation in EML Hematopoietic Precursor Cells by RNA-sequencing Analysis

Published on: November 11, 2014

12.6K
Mapping Genome-wide Accessible Chromatin in Primary Human T Lymphocytes by ATAC-Seq
09:08

Mapping Genome-wide Accessible Chromatin in Primary Human T Lymphocytes by ATAC-Seq

Published on: November 13, 2017

18.3K

Related Experiment Videos

Last Updated: Dec 9, 2025

Genome-wide Surveillance of Transcription Errors in Eukaryotic Organisms
09:30

Genome-wide Surveillance of Transcription Errors in Eukaryotic Organisms

Published on: September 13, 2018

9.8K
Identification of Key Factors Regulating Self-renewal and Differentiation in EML Hematopoietic Precursor Cells by RNA-sequencing Analysis
12:44

Identification of Key Factors Regulating Self-renewal and Differentiation in EML Hematopoietic Precursor Cells by RNA-sequencing Analysis

Published on: November 11, 2014

12.6K
Mapping Genome-wide Accessible Chromatin in Primary Human T Lymphocytes by ATAC-Seq
09:08

Mapping Genome-wide Accessible Chromatin in Primary Human T Lymphocytes by ATAC-Seq

Published on: November 13, 2017

18.3K

Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Long-read sequencing is crucial for understanding complex RNA transcript structures.
  • Existing hybrid correction algorithms are designed for genomic data and are unsuitable for transcriptomic data.
  • Transcriptome sequencing data presents unique challenges due to RNA expression variability and isoform complexity.

Purpose of the Study:

  • To develop a novel algorithm for correcting long-read sequencing errors in transcriptome studies.
  • To address the limitations of existing hybrid correction methods for RNA sequencing data.
  • To improve the accuracy and reliability of downstream RNA-seq analyses.

Main Methods:

  • Developed a reference-free algorithm named Transcript-level Aware Long-Read Correction (TALC).
  • Employed a weighted De Bruijn graph to model RNA expression and isoform representation.
  • Implemented TALC in C++ for efficient processing of transcriptome data.

Main Results:

  • TALC effectively corrects errors in long-read transcriptome sequencing data.
  • The transcript-level aware correction significantly enhances the accuracy of various downstream RNA-seq applications.
  • TALC demonstrates the necessity of specialized correction methods for long-read transcriptome analysis.

Conclusions:

  • TALC provides a robust solution for error correction in long-read RNA sequencing.
  • Improved accuracy from TALC is vital for reliable transcriptome profiling and analysis.
  • This novel algorithm advances the utility of long-read technologies in transcriptomics.