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

Genome Annotation and Assembly03:36

Genome Annotation and Assembly

The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
Labeling DNA Probes03:31

Labeling DNA Probes

DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
DNA Microarrays02:34

DNA Microarrays

Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
RNA-seq03:21

RNA-seq

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 microarray-based...
Gene Duplication and Divergence02:37

Gene Duplication and Divergence

The seminal work of Ohno in 1970 popularized the idea of gene duplication and divergence. DNA sequence comparison studies reveal that a large portion of the genes in bacteria, archaebacteria, and eukaryotes was  generated by gene duplication and divergence, indicating its critical role in evolution.
The duplicated copies of the gene are called Paralogs. Paralogs with similar sequences and functions form a gene family. Across several species, a large number of gene families are characterized.
Genomics02:02

Genomics

Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...

You might also read

Related Articles

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

Sort by
Same author

Organellar genomes of the putative Hawaiian endemic species Gibsmithia punonomaewa (Gigartinales, Rhodophyta): First available genomes for the Dumontiaceae.

Journal of phycology·2026
Same author

Prediction of mammographic breast density based on clinical breast ultrasound images using deep learning: a retrospective analysis.

Lancet regional health. Americas·2025
Same author

Deep Learning Predicts Interval and Screening-detected Cancer from Screening Mammograms: A Case-Case-Control Study in 6369 Women.

Radiology·2021
Same author

Placentas delivered by pre-pregnant obese women have reduced abundance and diversity in the microbiome.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology·2021
Same author

Gapless assembly of maize chromosomes using long-read technologies.

Genome biology·2020
Same author

Centromeric retrotransposons and centromere function.

Current opinion in genetics & development·2018

Related Experiment Video

Updated: Jun 17, 2026

A Web-Based Workflow for Selecting Gene- and Tissue-Specific Enhancers
08:12

A Web-Based Workflow for Selecting Gene- and Tissue-Specific Enhancers

Published on: July 18, 2025

JunctionViewer: customizable annotation software for repeat-rich genomic regions.

Thomas K Wolfgruber1, Gernot G Presting

  • 1Department of Molecular Biosciences and Bioengineering, University of Hawai'i at Mânoa, Honolulu, HI 96822, USA.

BMC Bioinformatics
|January 14, 2010
PubMed
Summary
This summary is machine-generated.

We developed JunctionViewer software to map maize centromeres and analyze their repetitive DNA sequences. This tool aids in understanding centromere arrangement and evolution across organisms.

More Related Videos

Inherent Dynamics Visualizer, an Interactive Application for Evaluating and Visualizing Outputs from a Gene Regulatory Network Inference Pipeline
10:44

Inherent Dynamics Visualizer, an Interactive Application for Evaluating and Visualizing Outputs from a Gene Regulatory Network Inference Pipeline

Published on: December 7, 2021

A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes
09:10

A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes

Published on: May 22, 2018

Related Experiment Videos

Last Updated: Jun 17, 2026

A Web-Based Workflow for Selecting Gene- and Tissue-Specific Enhancers
08:12

A Web-Based Workflow for Selecting Gene- and Tissue-Specific Enhancers

Published on: July 18, 2025

Inherent Dynamics Visualizer, an Interactive Application for Evaluating and Visualizing Outputs from a Gene Regulatory Network Inference Pipeline
10:44

Inherent Dynamics Visualizer, an Interactive Application for Evaluating and Visualizing Outputs from a Gene Regulatory Network Inference Pipeline

Published on: December 7, 2021

A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes
09:10

A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes

Published on: May 22, 2018

Area of Science:

  • Genomics
  • Bioinformatics
  • Molecular Biology

Background:

  • Centromeres, crucial for chromosome segregation, are challenging to study due to their repetitive DNA.
  • Maize centromeres, spanning megabases, require specialized tools for analysis and mapping.
  • Previous methods struggled with efficient analysis of large, repetitive genomic regions.

Purpose of the Study:

  • To map all ten maize centromeres onto the maize genetic map.
  • To characterize the sequence features of maize centromeres.
  • To develop specialized software for analyzing repetitive DNA in centromeric regions.

Main Methods:

  • Development of JunctionViewer, a novel annotation software.
  • Utilizing JunctionViewer to screen large maize genome datasets for repeat junctions.
  • Employing PCR with primers from repeat junctions to generate molecular markers.
  • Automating the identification and graphical display of centromeric repeats and features.

Main Results:

  • Successfully mapped all ten maize centromeres to the genetic map.
  • Characterized millions of nucleotides of centromeric DNA using JunctionViewer.
  • Identified key sequence features and gained insights into maize centromere arrangement and evolution.
  • Demonstrated JunctionViewer's efficiency in analyzing large genomic datasets.

Conclusions:

  • JunctionViewer automates the generation of graphical summaries for repetitive sequences.
  • The software is particularly valuable for identifying unique repeat junctions in centromeres.
  • Its scalability and customizable parameters make it ideal for ongoing genome projects.
  • Anticipated to facilitate the analysis of centromeres and other repeat-rich regions in diverse organisms.