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

Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

6.3K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
6.3K
CRISPR01:59

CRISPR

53.6K
Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
53.6K
CRISPR and crRNAs02:53

CRISPR and crRNAs

17.9K
Bacteria and archaea are susceptible to viral infections just like eukaryotes; therefore, they have developed a unique adaptive immune system to protect themselves. Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) are present in more than 45% of known bacteria and 90% of known archaea.
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
17.9K
The Antiviral System of Bacteria and Archaea: CRISPR01:23

The Antiviral System of Bacteria and Archaea: CRISPR

300
CRISPR stands for Clustered Regularly Interspaced Short Palindromic Repeats is a adaptive immune system found in bacteria and archaea that protects against viral infections. This system enables prokaryotic cells to identify, remember, and neutralize foreign genetic elements, primarily bacteriophages, by storing fragments of the invader’s DNA as a genetic memory.The CRISPR immune response begins during an initial infection. Cas (CRISPR-associated) proteins play a central role in this...
300
Homologous Recombination02:31

Homologous Recombination

56.3K
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
56.3K
Cis-regulatory Sequences02:02

Cis-regulatory Sequences

10.9K
Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
10.9K

You might also read

Related Articles

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

Sort by
Same author

Bioinformatics Meets Virology: The European Virus Bioinformatics Center's Second Annual Meeting.

Viruses·2018
Same author

Taxonomy of the family Arenaviridae and the order Bunyavirales: update 2018.

Archives of virology·2018
Same author

Evolution of Genome Architecture in Archaea: Spontaneous Generation of a New Chromosome in Haloferax volcanii.

Molecular biology and evolution·2018
Same author

Estimation of universal and taxon-specific parameters of prokaryotic genome evolution.

PloS one·2018
Same author

Vast diversity of prokaryotic virus genomes encoding double jelly-roll major capsid proteins uncovered by genomic and metagenomic sequence analysis.

Virology journal·2018
Same author

Taxonomy of the order Mononegavirales: update 2018.

Archives of virology·2018
Same journal

Evaluation of Prime Editing Efficiency in Human Immortalized MSC-TERT Cells with Osteogenic Potential for Modeling <i>FGFR2</i>-Linked Craniosynostosis.

The CRISPR journal·2026
Same journal

Induction of SpCas9-Directed Immune Responses Using Lipid Nanoparticles and Identification of SpCas9-Derived T Cell Epitopes in C57BL/6 Mice.

The CRISPR journal·2026
Same journal

Advice from the CRISPR Whisperer.

The CRISPR journal·2026
Same journal

CRISPR Learns to Read the Epigenome.

The CRISPR journal·2026
Same journal

Increasing the Effective Gene Drive Homing Rate by Targeting the Haploinsufficient Spermatogenesis Gene <i>Klhl10</i>.

The CRISPR journal·2026
Same journal

<i>Corrigendum to:</i> "Subtypes of Type I-E CRISPR-Cas Systems Distribution in Human <i>Escherichia coli</i> Isolates from China".

The CRISPR journal·2026
See all related articles

Related Experiment Video

Updated: Oct 23, 2025

CRISPR-Mediated Reorganization of Chromatin Loop Structure
09:20

CRISPR-Mediated Reorganization of Chromatin Loop Structure

Published on: September 14, 2018

12.8K

CRISPRclassify: Repeat-Based Classification of CRISPR Loci.

Matthew A Nethery1, Michael Korvink2, Kira S Makarova3

  • 1Genomic Sciences Graduate Program, North Carolina State University, Raleigh, North Carolina, USA; National Library of Medicine, Bethesda, Maryland, USA.

The CRISPR Journal
|August 18, 2021
PubMed
Summary
This summary is machine-generated.

This study introduces a novel machine learning method for detecting and classifying CRISPR-Cas systems in metagenomic data using repeat sequences. This cas-independent approach enhances the identification of unclassified CRISPR loci, improving genome editing research.

More Related Videos

HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries
10:10

HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries

Published on: March 31, 2019

8.5K
Author Spotlight: Development of Simplified CRISPR-Based Tests for Rapid Detection of Infectious Diseases
10:16

Author Spotlight: Development of Simplified CRISPR-Based Tests for Rapid Detection of Infectious Diseases

Published on: August 16, 2024

1.6K

Related Experiment Videos

Last Updated: Oct 23, 2025

CRISPR-Mediated Reorganization of Chromatin Loop Structure
09:20

CRISPR-Mediated Reorganization of Chromatin Loop Structure

Published on: September 14, 2018

12.8K
HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries
10:10

HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries

Published on: March 31, 2019

8.5K
Author Spotlight: Development of Simplified CRISPR-Based Tests for Rapid Detection of Infectious Diseases
10:16

Author Spotlight: Development of Simplified CRISPR-Based Tests for Rapid Detection of Infectious Diseases

Published on: August 16, 2024

1.6K

Area of Science:

  • Bioinformatics
  • Genomics
  • Computational Biology

Background:

  • CRISPR-Cas systems are crucial for genome editing and are typically identified by proximate cas genes.
  • Metagenomic data analysis presents challenges for traditional cas-gene-based CRISPR detection.
  • Unclassified CRISPR loci are often missed by current reference-based identification methods.

Purpose of the Study:

  • To develop a cas-independent machine learning approach for CRISPR locus detection and classification.
  • To identify CRISPR loci using repeat sequences, overcoming limitations of cas-gene-based methods.
  • To enable accurate classification of CRISPR loci in metagenomic datasets and fragmented assemblies.

Main Methods:

  • Utilized biological attributes of CRISPR repeat sequences as core features.
  • Applied machine learning algorithms, incorporating natural language processing techniques.
  • Trained and evaluated a model on an extensive set of metagenomes.

Main Results:

  • Achieved an overall F1 score of 0.82 for CRISPR locus classification.
  • Attained an F1 score of 0.97 for classifications with probabilities >0.85.
  • Demonstrated high performance on novel repeats with an F1 score of 0.96.

Conclusions:

  • The developed machine learning model accurately classifies CRISPR loci using a cas-independent, repeat-based approach.
  • This method effectively identifies unclassified CRISPR loci in metagenomic data where cas gene information is unavailable.
  • CRISPRclassify offers an efficient alternative for CRISPR locus classification in challenging genomic contexts.