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

Evolutionary Relationships through Genome Comparisons02:54

Evolutionary Relationships through Genome Comparisons

7.2K
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...
7.2K
Sanger Sequencing01:57

Sanger Sequencing

777.3K
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
777.3K
Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

19.1K
Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
19.1K

You might also read

Related Articles

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

Sort by
Same author

Global seroprevalence of neutralizing antibodies against adeno-associated virus serotypes used for human gene therapies.

Molecular therapy. Methods & clinical development·2024
Same author

Using large language models for safety-related table summarization in clinical study reports.

JAMIA open·2024
Same author

Development of PF-06671008, a Highly Potent Anti-P-cadherin/Anti-CD3 Bispecific DART Molecule with Extended Half-Life for the Treatment of Cancer.

Antibodies (Basel, Switzerland)·2019
Same author

Artificial Intelligence for Pharma: Time for Internal Investment.

Trends in pharmacological sciences·2019
Same author

A kinome-wide siRNA screen identifies multiple roles for protein kinases in hypoxic stress adaptation, including roles for IRAK4 and GAK in protection against apoptosis in VHL-/- renal carcinoma cells, despite activation of the NF-κB pathway.

Journal of biomolecular screening·2013
Same author

miRNA Alterations Modify Kinase Activation In The IGF-1 Pathway And Correlate With Colorectal Cancer Stage And Progression In Patients.

Journal of Cancer·2011

Related Experiment Video

Updated: Mar 17, 2026

An Integrated Approach for Microprotein Identification and Sequence Analysis
09:37

An Integrated Approach for Microprotein Identification and Sequence Analysis

Published on: July 12, 2022

4.1K

CATO: The Clone Alignment Tool.

Peter V Henstock1, Peter LaPan2

  • 1Pfizer R&D Business Technologies, 1 Burtt Road, Andover, MA, United States of America.

Plos One
|July 27, 2016
PubMed
Summary

High-throughput cloning generates many sequences requiring analysis. CATO, the Clone Alignment Tool, integrates alignment, editing, and selection into one software, streamlining cloning workflows.

Area of Science:

  • Molecular Biology
  • Bioinformatics
  • Genomics

Background:

  • High-throughput cloning generates vast sequence data.
  • Existing workflows require multiple software tools for sequence analysis.
  • Efficient management of clone sequences is crucial for research.

Purpose of the Study:

  • To develop a unified software solution for analyzing high-throughput cloning sequences.
  • To streamline the process of sequence alignment, editing, and selection.
  • To facilitate the integration of clone sequence analysis into existing bioinformatics pipelines.

Main Methods:

  • Developed CATO (Clone Alignment Tool), a single software application.
  • Implemented sequence alignment algorithms comparing candidate sequences to reference sequences.

More Related Videos

RNA Next-Generation Sequencing and a Bioinformatics Pipeline to Identify Expressed LINE-1s at the Locus-Specific Level
11:04

RNA Next-Generation Sequencing and a Bioinformatics Pipeline to Identify Expressed LINE-1s at the Locus-Specific Level

Published on: May 19, 2019

10.6K
A Practical Guide to Phylogenetics for Nonexperts
12:00

A Practical Guide to Phylogenetics for Nonexperts

Published on: February 5, 2014

36.2K

Related Experiment Videos

Last Updated: Mar 17, 2026

An Integrated Approach for Microprotein Identification and Sequence Analysis
09:37

An Integrated Approach for Microprotein Identification and Sequence Analysis

Published on: July 12, 2022

4.1K
RNA Next-Generation Sequencing and a Bioinformatics Pipeline to Identify Expressed LINE-1s at the Locus-Specific Level
11:04

RNA Next-Generation Sequencing and a Bioinformatics Pipeline to Identify Expressed LINE-1s at the Locus-Specific Level

Published on: May 19, 2019

10.6K
A Practical Guide to Phylogenetics for Nonexperts
12:00

A Practical Guide to Phylogenetics for Nonexperts

Published on: February 5, 2014

36.2K
  • Integrated multi-level visualization tools for sequence analysis.
  • Ensured compatibility with standard data formats for pipeline integration.
  • Main Results:

    • CATO enables alignment, evaluation, editing, and selection of clone sequences.
    • Provides three levels of visualization: summary, focused alignment, and pair-wise alignment.
    • Allows users to define matching criteria and edit reference sequences.
    • Outputs results to a summary file for workflow integration.

    Conclusions:

    • CATO simplifies and accelerates the analysis of high-throughput cloning experiments.
    • Offers a comprehensive solution for managing and validating clone sequences.
    • Enhances the efficiency of molecular cloning and genomic research workflows.