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

Long-patch Base Excision Repair01:02

Long-patch Base Excision Repair

8.3K
Since the discovery of the two BER pathways, there has been a debate about how a cell chooses one pathway over the other and the factors determining this selection. Numerous in vitro experiments have pointed out multiple determinants for the sub-pathway selection. These are:
8.3K

You might also read

Related Articles

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

Sort by
Same author

Extensive variation between chromosomes of North American and European hop.

Nature communications·2026
Same author

Dormancy Versus Germination: 3D Protein Modeling and Evolutionary Analyses Define the Roles of Genetic Variants in the Barley MKK3 Enzyme.

International journal of molecular sciences·2026
Same author

Mosquito sex separation using complementation of selectable traits and engineered neo-sex chromosomes.

Nature communications·2025
Same author

Detection of sex chromosomes in Tephritid pests using R-CQ and KAMY, two computational methods to support generic pest management applications.

Insect science·2025
Same author

Postdomestication selection of MKK3 shaped seed dormancy and end-use traits in barley.

Science (New York, N.Y.)·2025
Same author

CRISPR/Cas9-mediated mutagenesis of the white-eye gene in the tephritid pest Bactrocera zonata.

Insect science·2025

Related Experiment Video

Updated: Mar 31, 2026

BEST: Barcode Enabled Sequencing of Tetrads
12:59

BEST: Barcode Enabled Sequencing of Tetrads

Published on: May 1, 2014

10.6K

DNA Barcoding through Quaternary LDPC Codes.

Elizabeth Tapia1, Flavio Spetale1, Flavia Krsticevic2

  • 1CIFASIS-Conicet Institute, Rosario, Argentina; Fac. de Cs. Exactas e Ingeniería, Universidad Nac. de Rosario, Rosario, Argentina.

Plos One
|October 23, 2015
PubMed
Summary

New barcodes using quaternary Low Density Parity Check (LDPC) codes improve Next-Generation Sequencing (NGS) multiplexing accuracy. These advanced error-correcting codes reduce sample misidentification and read losses for large-scale sequencing applications.

More Related Videos

Flow-pattern Guided Fabrication of High-density Barcode Antibody Microarray
09:05

Flow-pattern Guided Fabrication of High-density Barcode Antibody Microarray

Published on: January 6, 2016

22.3K
Genetic Barcoding with Fluorescent Proteins for Multiplexed Applications
13:14

Genetic Barcoding with Fluorescent Proteins for Multiplexed Applications

Published on: April 14, 2015

9.9K

Related Experiment Videos

Last Updated: Mar 31, 2026

BEST: Barcode Enabled Sequencing of Tetrads
12:59

BEST: Barcode Enabled Sequencing of Tetrads

Published on: May 1, 2014

10.6K
Flow-pattern Guided Fabrication of High-density Barcode Antibody Microarray
09:05

Flow-pattern Guided Fabrication of High-density Barcode Antibody Microarray

Published on: January 6, 2016

22.3K
Genetic Barcoding with Fluorescent Proteins for Multiplexed Applications
13:14

Genetic Barcoding with Fluorescent Proteins for Multiplexed Applications

Published on: April 14, 2015

9.9K

Area of Science:

  • Genomics and Bioinformatics
  • Molecular Biology and Genetics

Background:

  • Next-Generation Sequencing (NGS) requires efficient barcoding for multiplexing numerous samples.
  • Existing barcoding systems using short random error-correcting codes limit multiplexing accuracy and scalability.
  • Previous attempts with binary BCH and pseudo-quaternary Hamming codes faced limitations in barcode size flexibility or error correction capabilities.

Purpose of the Study:

  • To design novel barcodes for high-throughput NGS applications.
  • To evaluate the performance of shortened binary BCH codes and quaternary Low Density Parity Check (LDPC) codes for barcoding.
  • To identify the most advantageous coding strategy for accurate sample multiplexing in the presence of sequencing errors.

Main Methods:

  • Design of barcoding systems utilizing shortened binary BCH codes.
  • Development of barcoding systems based on quaternary Low Density Parity Check (LDPC) codes.
  • Extensive simulations to assess barcode performance under varying mismatch error rates.

Main Results:

  • Both BCH and LDPC codes enable accurate barcoding with high multiplexing capacity.
  • Quaternary LDPC codes demonstrate superior performance, offering lower rates of read losses and undetected sample misidentification errors.
  • 24-nt LDPC barcodes can multiplex approximately 2000 samples with a misidentification error rate of 10(-9) and read loss rate of 10(-6) at a 10(-2) mismatch error rate.

Conclusions:

  • Quaternary LDPC codes represent a significant advancement for NGS barcoding.
  • LDPC-based barcodes provide enhanced accuracy and scalability for large-scale sample multiplexing.
  • This approach effectively addresses the limitations of current barcoding systems in high-error sequencing environments.