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 Experiment Videos

Exon discovery by genomic sequence alignment.

Burkhard Morgenstern1, Oliver Rinner, Saïd Abdeddaïm

  • 1GSF Research Center, MIPS/Institute of Bioinformatics, Ingolstädter Landstrasse 1, 85764 Neuherberg, Germany. burkhard@TechFak.Uni-Bielefeld.DE

Bioinformatics (Oxford, England)
|June 21, 2002
PubMed
Summary
This summary is machine-generated.

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

Extensive variation between chromosomes of North American and European hop.

Nature communications·2026
Same author

Under salt stress, quinoa stomatal guard cells control transpiration in an ABA-primed manner.

The New phytologist·2025
Same author

Author Correction: A pangenome and pantranscriptome of hexaploid oat.

Nature·2025
Same author

Whole-genome resequencing of the wild barley diversity collection: a resource for identifying and exploiting genetic variation for cultivated barley improvement.

G3 (Bethesda, Md.)·2025
Same author

A pangenome and pantranscriptome of hexaploid oat.

Nature·2025
Same author

De novo annotation reveals transcriptomic complexity across the hexaploid wheat pan-genome.

Nature communications·2025
Same journal

3DICE: Interpretable 3D Cross-Modal Learning for Drug-Target Interaction Prediction and Large-Scale Drug Discovery.

Bioinformatics (Oxford, England)·2026
Same journal

KASSPer: Kinase Active Site Structure Prediction using Protein and Ligand Language Models and Its Application to Virtual Screening.

Bioinformatics (Oxford, England)·2026
Same journal

IDR searcher: a search engine solution for public image resources.

Bioinformatics (Oxford, England)·2026
Same journal

KCFtools: Rapid alignment-free method for introgression screening and GWAS using k-mer profiles.

Bioinformatics (Oxford, England)·2026
Same journal

Meta2DB: Curated shotgun metagenomic feature sets and metadata for health state prediction.

Bioinformatics (Oxford, England)·2026
Same journal

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

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

Local sequence similarity aids in identifying functional genomic elements. A new DIALIGN implementation improves alignment of large DNA sequences, showing high correlation with protein-coding regions, with DIALIGN being most specific.

Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Functional genomic regions are conserved during evolution, making local sequence similarity an indicator of biological function.
  • Cross-species sequence comparison is a powerful method for identifying functional elements in large eukaryotic DNA sequences.
  • Comparative gene-finding approaches offer advantages over traditional methods by not requiring species-specific training data or existing gene databases.

Purpose of the Study:

  • To introduce a new implementation of the DIALIGN sequence-alignment program optimized for large genomic sequences.
  • To evaluate the performance of the new DIALIGN implementation against other alignment tools for gene prediction.

Main Methods:

  • Development of an enhanced DIALIGN program for aligning large-scale genomic sequences.

Related Experiment Videos

  • Comparative analysis of DIALIGN against PipMaker, WABA, and BLAST using sequence similarity metrics.
  • Assessment of the correlation between identified local similarities and protein-coding regions.
  • Main Results:

    • The new DIALIGN implementation effectively aligns large genomic sequences.
    • Local similarities identified by comparative methods are highly correlated with protein-coding regions.
    • PipMaker demonstrated the highest sensitivity, while DIALIGN exhibited the highest specificity in identifying functional elements.

    Conclusions:

    • Comparative sequence analysis, particularly using alignment tools like DIALIGN, is crucial for identifying functional genomic regions.
    • The enhanced DIALIGN program provides a specific and reliable method for genomic sequence alignment and functional element discovery.