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

Multiple sequence alignments of partially coding nucleic acid sequences.

Roman R Stocsits1, Ivo L Hofacker, Claudia Fried

  • 1Interdisciplinary Centre for Bioinformatics, University of Leipzig, Haertelstrasse 16-18, D-04107 Leipzig, Germany. roman@bioinf.uni-leipzig.de

BMC Bioinformatics
|June 30, 2005
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

Rational design of mechanically active RNAs: de novo engineering of functional exoribonuclease-resistant RNAs.

Nucleic acids research·2026
Same author

Sequence Design for RNA-RNA Interactions.

Methods in molecular biology (Clifton, N.J.)·2024
Same author

Sampling globally and locally correct RNA 3D structures using Ernwin, SPQR and experimental SAXS data.

Nucleic acids research·2024
Same author

tRNA expression and modification landscapes, and their dynamics during zebrafish embryo development.

Nucleic acids research·2024
Same author

Comparative RNA Genomics.

Methods in molecular biology (Clifton, N.J.)·2024
Same author

The Multiscale Ernwin/SPQR RNA Structure Prediction Pipeline.

Methods in molecular biology (Clifton, N.J.)·2024
Same journal

OpenIMC: an open-source platform for analyzing single-cell and spatial proteomics by imaging mass cytometry.

BMC bioinformatics·2026
Same journal

NAP: an open source pipeline for cross-domain microbiome profiling using Nanopore sequencing-derived amplicon data.

BMC bioinformatics·2026
Same journal

SurvGME: an R package for survival analysis with graphical and measurement error models.

BMC bioinformatics·2026
Same journal

SimMapNet: a Bayesian framework for gene regulatory network inference using gene ontology similarities as external hint.

BMC bioinformatics·2026
Same journal

Dual channel drug-drug interactions extraction based on cross attention.

BMC bioinformatics·2026
Same journal

FeSseqdb: a curated sequence-level database and interpretable machine learning framework for identifying iron-sulfur proteins.

BMC bioinformatics·2026
See all related articles

This study introduces codaln, a novel tool for aligning RNA and DNA sequences using both nucleic acid and amino acid information. This combined approach improves alignment quality for genomic data analysis.

Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • High-quality sequence alignment is crucial for comparative genomics.
  • Nucleic acid sequences show greater heterogeneity than protein sequences due to genetic code redundancy.
  • Aligning coding nucleic acid sequences using amino acid information is desirable, especially with partial translations or overlapping reading frames.

Purpose of the Study:

  • To develop a multiple alignment tool incorporating both nucleic acid and amino acid sequence information.
  • To address challenges in aligning coding sequences with complex translation patterns, such as in RNA viruses.

Main Methods:

  • Developed codaln, a tool implementing a combined nucleic acid and amino acid scoring model.
  • Supports pairwise and progressive multiple alignments with flexible parameter weighting.

Related Experiment Videos

  • Resource requirements are comparable to standard tools like ClustalW.
  • Main Results:

    • Demonstrated codaln's applicability to diverse sequences like bacteriophage Levivirus and Vertebrate Hox clusters.
    • Showed that combining nucleic acid and amino acid data significantly improves alignment quality.
    • Validated the tool's effectiveness in enhancing downstream analyses.

    Conclusions:

    • The combined scoring model in codaln offers superior alignment accuracy for coding sequences.
    • Improved alignments enhance the performance of tools dependent on accurate sequence data, such as RNA secondary structure prediction.
    • codaln represents a valuable advancement for genomic sequence analysis.