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.
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...
Evolutionary Relationships through Genome Comparisons02:54

Evolutionary Relationships through Genome Comparisons

Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...

You might also read

Related Articles

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

Sort by
Same author

A Non-Canonical Role for Hepatocyte MLKL in Promoting Mitochondrial Dysfunction and Senescence in the Aging Liver.

Aging cell·2026
Same author

Striatal Dysregulation of Angpt2 and Circadian Gene Expression in a Rotenone Rat Model of Parkinson's Disease.

Journal of molecular neuroscience : MN·2026
Same author

Beyond blacklists: a critical assessment of exclusion set generation strategies and alternative approaches.

Bioinformatics (Oxford, England)·2026
Same author

Daraxonrasib (RMC-6236) is an effective targeted therapy for <i>RAS</i> -mutant neuroblastoma.

bioRxiv : the preprint server for biology·2026
Same author

Therapeutic synergies that overcome carboplatin resistance in triple-negative breast cancer.

Journal of experimental & clinical cancer research : CR·2026
Same author

Type I interferon drives dysfunction of a distinct CD8+ HLA-DRB1+ T cell subset in systemic lupus erythematosus.

medRxiv : the preprint server for health sciences·2026

Related Experiment Video

Updated: May 26, 2026

Introductory Analysis and Validation of CUT&#38;RUN Sequencing Data
04:58

Introductory Analysis and Validation of CUT&RUN Sequencing Data

Published on: December 13, 2024

GenomeRunner: automating genome exploration.

Mikhail G Dozmorov1, Lukas R Cara, Cory B Giles

  • 1Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104-5005, USA. mikhail-dozmorov@omrf.org

Bioinformatics (Oxford, England)
|December 14, 2011
PubMed
Summary
This summary is machine-generated.

GenomeRunner automates the analysis of high-throughput genomic data, identifying biological implications and commonalities within significant genomic regions. This tool aids in interpreting complex genomic study results by associating experimental features with annotated genomic features.

More Related Videos

A Bioinformatics Pipeline for Investigating Molecular Evolution and Gene Expression using RNA-seq
07:09

A Bioinformatics Pipeline for Investigating Molecular Evolution and Gene Expression using RNA-seq

Published on: May 28, 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: May 26, 2026

Introductory Analysis and Validation of CUT&#38;RUN Sequencing Data
04:58

Introductory Analysis and Validation of CUT&RUN Sequencing Data

Published on: December 13, 2024

A Bioinformatics Pipeline for Investigating Molecular Evolution and Gene Expression using RNA-seq
07:09

A Bioinformatics Pipeline for Investigating Molecular Evolution and Gene Expression using RNA-seq

Published on: May 28, 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
  • Computational Biology

Background:

  • Interpreting high-throughput genomic studies (e.g., GWAS, ChIP-seq) is challenging due to their open-ended nature.
  • Identifying biological implications and genome-wide commonalities among statistically significant regions requires analyzing numerous annotated genomic features.
  • Prioritizing which genomic features to analyze is difficult in a hypothesis-free manner.

Purpose of the Study:

  • To provide partial automation for examining associations between experimental features and annotated genomic regions.
  • To enable data-driven, hypothesis-free analysis of genomic study results.
  • To address the challenge of interpreting large-scale genomic datasets.

Main Methods:

  • Developed GenomeRunner, a tool for automating the annotation and enrichment of genomic features of interest (FOI) with annotated genomic features (GFs).
  • GenomeRunner supports analysis across different organisms.
  • The tool performs both simple association of FOIs with known GFs and statistical testing for group associations.

Main Results:

  • GenomeRunner automates the annotation and enrichment process for genomic features.
  • The tool facilitates the identification of biological implications and genome-wide patterns within significant genomic regions.
  • It enables testing for statistical associations between sets of enriched genomic features.

Conclusions:

  • GenomeRunner offers a valuable solution for the automated interpretation of high-throughput genomic studies.
  • The tool aids researchers in uncovering biological insights from complex genomic data.
  • It supports a data-driven approach to genomic feature analysis.