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

22.3K
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.
22.3K
Evolutionary Relationships through Genome Comparisons02:54

Evolutionary Relationships through Genome Comparisons

7.3K
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...
7.3K
Genome Size and the Evolution of New Genes03:21

Genome Size and the Evolution of New Genes

3.7K
3.7K

You might also read

Related Articles

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

Sort by
Same author

Clinical risk factors predicting likelihood of pathogenic genetic result in NICU patients.

Genetics in medicine open·2026
Same author

Signatures of sex ratio distortion in humans.

bioRxiv : the preprint server for biology·2026
Same author

Quantifying lifetime risk for 1,401 infectious diseases across the diabetes spectrum using a Bayesian approach.

BMC medicine·2026
Same author

Phenotype-first patient matching with SimPheny identifies diagnostic candidates beyond curated gene associations.

medRxiv : the preprint server for health sciences·2026
Same author

Genome x Environment analysis of Sudden Unexpected Infant Death unveils etiologic heterogeneity and strong cannabis and genetic disease risks.

medRxiv : the preprint server for health sciences·2025
Same author

Generalisability of Maternal Genetic Risk Score for Birth Weight Across Racial Identity and Ancestry: A Secondary Analysis of a Prospective Cohort Study.

BJOG : an international journal of obstetrics and gynaecology·2025
Same journal

Protein Sequence Analysis Using the MPI Bioinformatics Toolkit.

Current protocols in bioinformatics·2020
Same journal

Exploring Manually Curated Annotations of Intrinsically Disordered Proteins with DisProt.

Current protocols in bioinformatics·2020
Same journal

Network Building with the Cytoscape BioGateway App Explained in Five Use Cases.

Current protocols in bioinformatics·2020
Same journal

Expanding the Perseus Software for Omics Data Analysis With Custom Plugins.

Current protocols in bioinformatics·2020
Same journal

Exploring Non-Coding RNAs in RNAcentral.

Current protocols in bioinformatics·2020
Same journal

How to Illuminate the Dark Proteome Using the Multi-omic OpenProt Resource.

Current protocols in bioinformatics·2020
See all related articles

Related Experiment Video

Updated: Apr 19, 2026

Informatic Analysis of Sequence Data from Batch Yeast 2-Hybrid Screens
09:14

Informatic Analysis of Sequence Data from Batch Yeast 2-Hybrid Screens

Published on: June 28, 2018

7.6K

Genome Annotation and Curation Using MAKER and MAKER-P.

Michael S Campbell1, Carson Holt1,2, Barry Moore1,2

  • 1Eccles Institute of Human Genetics, University of Utah, Salt Lake City, Utah.

Current Protocols in Bioinformatics
|December 16, 2014
PubMed
Summary
This summary is machine-generated.

This study details using MAKER and MAKER-P genome annotation tools to analyze protein-coding and RNA genes in new genomes. These scalable tools efficiently update, combine, and map gene annotations with quality metrics.

Keywords:
comparative genomicsgene findinggenome annotationplants

More Related Videos

Author Spotlight: Investigating the Role of Repetitive DNA Misregulation in Cancer Initiation and Immunotherapy Resistance
04:58

Author Spotlight: Investigating the Role of Repetitive DNA Misregulation in Cancer Initiation and Immunotherapy Resistance

Published on: December 13, 2024

4.9K
Comprehensive Workflow for the Genome-wide Identification and Expression Meta-analysis of the ATL E3 Ubiquitin Ligase Gene Family in Grapevine
10:40

Comprehensive Workflow for the Genome-wide Identification and Expression Meta-analysis of the ATL E3 Ubiquitin Ligase Gene Family in Grapevine

Published on: December 22, 2017

11.1K

Related Experiment Videos

Last Updated: Apr 19, 2026

Informatic Analysis of Sequence Data from Batch Yeast 2-Hybrid Screens
09:14

Informatic Analysis of Sequence Data from Batch Yeast 2-Hybrid Screens

Published on: June 28, 2018

7.6K
Author Spotlight: Investigating the Role of Repetitive DNA Misregulation in Cancer Initiation and Immunotherapy Resistance
04:58

Author Spotlight: Investigating the Role of Repetitive DNA Misregulation in Cancer Initiation and Immunotherapy Resistance

Published on: December 13, 2024

4.9K
Comprehensive Workflow for the Genome-wide Identification and Expression Meta-analysis of the ATL E3 Ubiquitin Ligase Gene Family in Grapevine
10:40

Comprehensive Workflow for the Genome-wide Identification and Expression Meta-analysis of the ATL E3 Ubiquitin Ligase Gene Family in Grapevine

Published on: December 22, 2017

11.1K

Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Accurate genome annotation is crucial for understanding gene function and biological processes.
  • Existing annotation pipelines may require updates or integration with new data.
  • Ensuring annotation quality and consistency across different datasets is a persistent challenge.

Purpose of the Study:

  • To describe the application of MAKER and MAKER-P for comprehensive genome annotation.
  • To demonstrate the utility of these tools for updating, combining, and validating gene annotations.
  • To highlight the scalability and efficiency of MAKER/MAKER-P for genomes of varying sizes.

Main Methods:

  • Utilized the MAKER and MAKER-P software packages for genome annotation.
  • Applied the tools to annotate protein-coding and noncoding RNA genes.
  • Integrated new evidence to update and combine legacy annotations.
  • Incorporated quality metrics and mapped annotations to new genome assemblies.

Main Results:

  • Successfully annotated protein-coding and noncoding RNA genes in newly assembled genomes.
  • Effectively updated and combined existing gene annotations using new evidence.
  • Added valuable quality metrics to annotations generated by other pipelines.
  • Demonstrated the ability to map existing annotations to new genome assemblies.

Conclusions:

  • MAKER and MAKER-P are versatile and efficient tools for robust genome annotation.
  • These platforms facilitate the integration of diverse annotation data and quality assessment.
  • The scalability of MAKER/MAKER-P supports diverse genomic research needs, regardless of genome size.