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

Overview of Transposition and Recombination02:13

Overview of Transposition and Recombination

15.9K
Transposons make up a significant part of genomes of various organisms. Therefore, it is believed that transposition played a major evolutionary role in speciation by changing genome sizes and modifying gene expression patterns. For example, in bacteria, transposition can lead to conferring antibiotic resistance. Movement of transposable elements within the genetic pool of pathogenic bacteria can aid in transfer of antibiotic-resistant genetic elements. In eukaryotes, transposons can carry out...
15.9K
Homologous Recombination02:31

Homologous Recombination

4.7K
4.7K
Tandem Mass Spectrometry01:21

Tandem Mass Spectrometry

1.1K
Tandem mass spectrometry is a technique that uses multiple mass analyzers in series to obtain a higher selectivity and signal-to-noise ratio for the analyte. Instruments with multiple analyzers separated by an interaction cell enable secondary fragmentation and selected study of the fragment ions.
Secondary fragmentations occur in the interaction cell and can be induced by various factors. Fragmentation induced by collision with inert gases, such as N2, Ar, He, etc., is called collision-induced...
1.1K
The Replisome03:01

The Replisome

6.7K
6.7K
DNA Base Pairing02:27

DNA Base Pairing

27.6K
27.6K
Peptide Identification Using Tandem Mass Spectrometry01:33

Peptide Identification Using Tandem Mass Spectrometry

6.6K
Tandem mass spectrometry, also known as MS/MS or MS2, is an analytical technique that employs two mass analyzers. Essentially it is a series of mass spectrometers that helps isolate a particular biomolecule and then helps study its chemical properties.
This technique helps gather information regarding the protein from which the peptide was obtained and to study the peptides’ amino acid sequence. Identifying peptides from a complex mixture is an important component of the growing field of...
6.6K

You might also read

Related Articles

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

Sort by
Same author

DipSkmer: Reference-free population genomics with diploid genome skims.

bioRxiv : the preprint server for biology·2026
Same author

Preservation and clonal behavior of extrachromosomal DNA in patient-derived xenograft models of childhood cancers.

Genome medicine·2026
Same author

ReSkmer: modeling repeats allows k-mer-based alignment-free methods to calculate population genomic distances.

Genome biology·2026
Same author

High-depth whole genome sequencing of premalignant breast lesions reveals rearrangement hotspots and personalized management opportunities.

Nature communications·2026
Same author

It Takes 2 (Repeats) to Lose TANGO2.

Neurology. Genetics·2026
Same author

Fast and accurate resolution of ecDNA sequence using Cycle-Extractor.

bioRxiv : the preprint server for biology·2026
Same journal

Region-aware bridge modeling enables interpretable mesoscale representation of spatial transcriptomic tissue sections.

Bioinformatics advances·2026
Same journal

Microbiome differential abundance methodologies to detect relevant taxa associated with chemotherapy toxicity rate in colorectal cancer.

Bioinformatics advances·2026
Same journal

maldipickr dereplicates microbial MALDI-TOF spectra to facilitate multiplexed isolation.

Bioinformatics advances·2026
Same journal

RAM-MSA: an anytime memory-bounded method for exact multiple sequence alignment using path finding.

Bioinformatics advances·2026
Same journal

Interpretable machine learning for low-sample multi-omics: a case study of ferret vaccine response.

Bioinformatics advances·2026
Same journal

DeepTaxa: a hybrid CNN-BERT framework for 16S rRNA taxonomic classification.

Bioinformatics advances·2026
See all related articles

Related Experiment Video

Updated: Jul 30, 2025

Novel Sequence Discovery by Subtractive Genomics
09:40

Novel Sequence Discovery by Subtractive Genomics

Published on: January 25, 2019

8.7K

TRviz: a Python library for decomposing and visualizing tandem repeat sequences.

Jonghun Park1, Eli Kaufman2, Paul N Valdmanis2

  • 1Department of Computer Science & Engineering, University of California, San Diego, La Jolla, CA 92093, USA.

Bioinformatics Advances
|May 11, 2023
PubMed
Summary
This summary is machine-generated.

TRviz is a new Python tool for analyzing tandem repeat (TR) sequences. It helps visualize the motif composition within TR alleles, aiding genetic research.

More Related Videos

DNA Fingerprinting of Mycobacterium leprae Strains Using Variable Number Tandem Repeat VNTR - Fragment Length Analysis FLA
09:39

DNA Fingerprinting of Mycobacterium leprae Strains Using Variable Number Tandem Repeat VNTR - Fragment Length Analysis FLA

Published on: July 15, 2011

27.3K
Genotypic Inference of HIV-1 Tropism Using Population-based Sequencing of V3
11:10

Genotypic Inference of HIV-1 Tropism Using Population-based Sequencing of V3

Published on: December 27, 2010

12.3K

Related Experiment Videos

Last Updated: Jul 30, 2025

Novel Sequence Discovery by Subtractive Genomics
09:40

Novel Sequence Discovery by Subtractive Genomics

Published on: January 25, 2019

8.7K
DNA Fingerprinting of Mycobacterium leprae Strains Using Variable Number Tandem Repeat VNTR - Fragment Length Analysis FLA
09:39

DNA Fingerprinting of Mycobacterium leprae Strains Using Variable Number Tandem Repeat VNTR - Fragment Length Analysis FLA

Published on: July 15, 2011

27.3K
Genotypic Inference of HIV-1 Tropism Using Population-based Sequencing of V3
11:10

Genotypic Inference of HIV-1 Tropism Using Population-based Sequencing of V3

Published on: December 27, 2010

12.3K

Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Tandem repeats (TRs) are repetitive DNA sequences.
  • Analyzing TR sequences and their motif composition is crucial for understanding genetic variation and disease.
  • Existing tools may lack comprehensive features for TR sequence decomposition, encoding, alignment, and visualization.

Purpose of the Study:

  • To introduce TRviz, an open-source Python library for the comprehensive analysis of tandem repeat sequences.
  • To provide a user-friendly tool for decomposing, encoding, aligning, and visualizing TR sequences and their motif compositions.
  • To facilitate the study of genetic variation and its impact through advanced TR analysis.

Main Methods:

  • TRviz utilizes Python to process collections of TR-containing sequences (alleles).
  • The library accepts one or more defined motifs as input for analysis.
  • It generates visualizations that depict the motif composition of each TR sequence.

Main Results:

  • TRviz successfully decomposes, encodes, aligns, and visualizes TR sequences.
  • The tool produces plots illustrating the specific motif composition within TR alleles.
  • This enables a clear understanding of the structural variations in TR regions.

Conclusions:

  • TRviz offers a powerful and accessible solution for tandem repeat sequence analysis.
  • The library's visualization capabilities enhance the interpretation of genetic data related to TRs.
  • TRviz is a valuable resource for researchers in genomics and bioinformatics studying repetitive DNA elements.