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

Homologous Recombination02:31

Homologous Recombination

50.5K
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...
50.5K
RNA-seq03:21

RNA-seq

10.0K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
10.0K
Mismatch Repair01:36

Mismatch Repair

40.1K
Overview
40.1K

You might also read

Related Articles

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

Sort by
Same author

Deep PACBED: Multitask analysis of PACBED images using deep neural networks.

Ultramicroscopy·2026
Same author

Clinical, Dietary, Lifestyle and Genetic Factors Associated With Age at Onset of Esophageal Adenocarcinoma.

United European gastroenterology journal·2026
Same author

Generalization of ML Models Between ECG and VCG Representation.

Studies in health technology and informatics·2026
Same author

DicomShield: A Pseudonymization Proxy for the Secondary Use of Imaging Data in the Research Context.

Studies in health technology and informatics·2026
Same author

Harnessing generative AI for predicting and optimizing antimicrobial peptides against drug-resistant infections.

npj antimicrobials and resistance·2026
Same author

dcFCI: Robust Causal Discovery Under Latent Confounding, Unfaithfulness, and Mixed Data.

IEEE transactions on pattern analysis and machine intelligence·2026
Same journal

Correction to: Pathogenicity patterns in cytochrome P450 family.

Bioinformatics advances·2026
Same journal

Region-aware bridge modeling enables interpretable mesoscale representation of spatial transcriptomic tissue sections.

Bioinformatics advances·2026
Same journal

Microbiome differential abundance methodologies to detect relevant taxa associated with chemotherapy toxicity rate in colorectal cancer.

Bioinformatics advances·2026
Same journal

maldipickr dereplicates microbial MALDI-TOF spectra to facilitate multiplexed isolation.

Bioinformatics advances·2026
Same journal

RAM-MSA: an anytime memory-bounded method for exact multiple sequence alignment using path finding.

Bioinformatics advances·2026
Same journal

Interpretable machine learning for low-sample multi-omics: a case study of ferret vaccine response.

Bioinformatics advances·2026
See all related articles

Related Experiment Video

Updated: Jun 30, 2025

Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter
06:59

Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter

Published on: March 31, 2022

2.4K

RepairNatrix: a Snakemake workflow for processing DNA sequencing data for DNA storage.

Peter Michael Schwarz1, Marius Welzel1, Dominik Heider1

  • 1Department of Mathematics and Computer Science, University of Marburg, Marburg 35032, Germany.

Bioinformatics Advances
|March 18, 2024
PubMed
Summary
This summary is machine-generated.

RepairNatrix enhances DNA data storage by improving raw sequencing data processing. This workflow reduces the number of reads needed for error-free data decoding by up to 35x.

More Related Videos

gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of BRCA1, BRCA2, and 9 Genes Involved in DNA Damage Repair
08:15

gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of BRCA1, BRCA2, and 9 Genes Involved in DNA Damage Repair

Published on: October 6, 2014

12.3K
Methyl-binding DNA capture Sequencing for Patient Tissues
08:40

Methyl-binding DNA capture Sequencing for Patient Tissues

Published on: October 31, 2016

8.6K

Related Experiment Videos

Last Updated: Jun 30, 2025

Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter
06:59

Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter

Published on: March 31, 2022

2.4K
gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of BRCA1, BRCA2, and 9 Genes Involved in DNA Damage Repair
08:15

gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of BRCA1, BRCA2, and 9 Genes Involved in DNA Damage Repair

Published on: October 6, 2014

12.3K
Methyl-binding DNA capture Sequencing for Patient Tissues
08:40

Methyl-binding DNA capture Sequencing for Patient Tissues

Published on: October 31, 2016

8.6K

Area of Science:

  • Bioinformatics
  • Data Storage
  • Molecular Biology

Background:

  • DNA storage systems leverage biological molecules for data encoding.
  • Error-correcting and constrained codes are advancing DNA data storage.
  • Raw sequencing data processing remains a bottleneck for DNA storage efficiency.

Purpose of the Study:

  • To introduce RepairNatrix, a novel read-processing workflow for DNA storage.
  • To enhance the recoverability of encoded data by addressing errors in sequencing reads.
  • To enable fair and reproducible comparisons of different DNA storage approaches.

Main Methods:

  • Developed RepairNatrix, a workflow for preprocessing raw sequencing data.
  • Implemented functionality to flag and heuristically repair constraint-violating sequences.
  • Evaluated RepairNatrix against preprocessing strategies lacking repair capabilities.

Main Results:

  • RepairNatrix significantly improves the preprocessing of raw sequencing data for DNA storage.
  • The workflow effectively flags and repairs constraint-violating sequences, increasing data recoverability.
  • RepairNatrix reduced the required number of raw reads for successful, error-free decoding by 25-35x across datasets.

Conclusions:

  • RepairNatrix offers a tailored solution for DNA storage code processing.
  • The workflow enhances data integrity and reduces redundancy in DNA data storage.
  • RepairNatrix is publicly available on GitHub, promoting further research and development.