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

Maxam-Gilbert Sequencing01:05

Maxam-Gilbert Sequencing

In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
Challenges of the Maxam-Gilbert Method
The...
Multi-species Conserved Sequences02:51

Multi-species Conserved Sequences

Next-generation sequencing technologies have created large genomic databases of a variety of animals and plants. Ever since the human genome project was completed, scientists studied the genome of primates, mammals, and other phylogenetically distant living beings. Such large-scaleĀ  studies have provided new insights into the evolutionary relationship between organisms.
Although the genome of each species varies greatly from each other, a few sequences are highly conserved. Such conserved DNA...
Sanger Sequencing01:57

Sanger Sequencing

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...

You might also read

Related Articles

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

Sort by
Same author

Automated implementation of the SwabSeq COVID-19 diagnostic assay on the opentrons flex liquid-handling robot.

Diagnostic microbiology and infectious diseaseĀ·2026
Same author

FBApro: A fast, simple linear transformation for diverse metabolic modeling tasks.

ArXivĀ·2026
Same author

Fast, accurate construction of multiple sequence alignments from protein language embeddings.

bioRxiv : the preprint server for biologyĀ·2026
Same author

Single-cell transcriptomics reveals FXR1 as an actionable target for siRNA therapy in ovarian cancer.

Nature communicationsĀ·2026
Same author

Genome-wide association analyses of autoimmune hypothyroidism reveal autoimmune and thyroid-specific contributions and an inverse relationship with cancer risk.

Nature geneticsĀ·2026
Same author

Editorial Expression of Concern: Direct targeting of Sec23a by miR-200s influences cancer cell secretome and promotes metastatic colonization.

Nature medicineĀ·2026
Same journal

Cross-Domain Transfer Learning from Peptides to Metabolites Using a Multi-Property Fine-Tuned LLM.

Bioinformatics (Oxford, England)Ā·2026
Same journal

Biomedical Concept Recognition with Error-aware Negative-enhanced Ranking Framework.

Bioinformatics (Oxford, England)Ā·2026
Same journal

TEDLH: Domain HMMs for sensitive detection of remote homologues.

Bioinformatics (Oxford, England)Ā·2026
Same journal

PLNFGL: Joint Estimation of Multi-Condition Gene Networks from Single-cell RNA-seq Data.

Bioinformatics (Oxford, England)Ā·2026
Same journal

MCFST: Spatial domain identification method based on multi-view graph convolutional network and graph fusion network.

Bioinformatics (Oxford, England)Ā·2026
Same journal

SpaBiT: Enhancing Spatial Transcriptomics Resolution via Bidirectional Attention Transformers.

Bioinformatics (Oxford, England)Ā·2026
See all related articles

Related Experiment Video

Updated: Jun 23, 2026

A Practical Guide to Phylogenetics for Nonexperts
12:00

A Practical Guide to Phylogenetics for Nonexperts

Published on: February 5, 2014

A practical algorithm for finding maximal exact matches in large sequence datasets using sparse suffix arrays.

Zia Khan1, Joshua S Bloom, Leonid Kruglyak

  • 1Department of Computer Science, Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544, USA. zkhan@cs.princeton.edu

Bioinformatics (Oxford, England)
|April 25, 2009
PubMed
Summary
This summary is machine-generated.

A new algorithm efficiently finds maximal exact matches (MEMs) in large sequences using a sparse suffix array (SA). This approach reduces memory usage, enabling analysis of longer sequences for genome assembly and comparison.

More Related Videos

Primer Extension Capture: Targeted Sequence Retrieval from Heavily Degraded DNA Sources
15:28

Primer Extension Capture: Targeted Sequence Retrieval from Heavily Degraded DNA Sources

Published on: September 3, 2009

Single Cell Multiplex Reverse Transcription Polymerase Chain Reaction After Patch-clamp
10:44

Single Cell Multiplex Reverse Transcription Polymerase Chain Reaction After Patch-clamp

Published on: June 20, 2018

Related Experiment Videos

Last Updated: Jun 23, 2026

A Practical Guide to Phylogenetics for Nonexperts
12:00

A Practical Guide to Phylogenetics for Nonexperts

Published on: February 5, 2014

Primer Extension Capture: Targeted Sequence Retrieval from Heavily Degraded DNA Sources
15:28

Primer Extension Capture: Targeted Sequence Retrieval from Heavily Degraded DNA Sources

Published on: September 3, 2009

Single Cell Multiplex Reverse Transcription Polymerase Chain Reaction After Patch-clamp
10:44

Single Cell Multiplex Reverse Transcription Polymerase Chain Reaction After Patch-clamp

Published on: June 20, 2018

Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • High-throughput sequencing generates vast amounts of data, increasing demands on sequence analysis algorithms.
  • Maximal exact matches (MEMs) are crucial for genome assembly and comparative genomics.
  • Existing MEM algorithms struggle with the scale of modern sequencing data.

Purpose of the Study:

  • To develop a novel algorithm for efficiently computing MEMs.
  • To address the memory limitations of current MEM algorithms for large-scale sequence analysis.

Main Methods:

  • Introduced a new MEM algorithm utilizing a sparse suffix array (SA).
  • A sparse SA stores every K-th position, significantly reducing memory footprint compared to full text indexes.
  • The algorithm compensates for the sparse index by incorporating partial matches and additional text scanning.

Main Results:

  • The sparse SA-based algorithm achieves the same output as full text index algorithms under specific conditions.
  • The algorithm demonstrates reduced memory usage, enabling MEM computation for significantly longer sequences.
  • This method effectively trades increased computation for decreased memory consumption.

Conclusions:

  • The novel sparse SA algorithm offers a memory-efficient solution for MEM computation.
  • This advancement supports the analysis of larger datasets in high-throughput sequencing applications.
  • The algorithm is available as open-source software and can replace existing MEM algorithms in tools like MUMmer 3.