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

RNA-seq03:21

RNA-seq

9.2K
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...
9.2K
Next-generation Sequencing03:00

Next-generation Sequencing

87.4K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
87.4K
Sanger Sequencing01:57

Sanger Sequencing

800.2K
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...
800.2K

You might also read

Related Articles

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

Sort by
Same author

Toward Hydrogen Isotope Separations through Strong Hydrogen Adsorption at Open Copper(I) Sites in an Ultramicroporous Metal-Organic Framework.

Journal of the American Chemical Society·2026
Same author

An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autism.

Nature·2026
Same author

Mapping the inter- and intra-genic codon-usage landscape in <i>Homo sapiens</i>.

NAR genomics and bioinformatics·2026
Same author

Autism data sharing: Benefits, challenges, and recommendations.

PLOS digital health·2026
Same author

Multimodal Nanoscale Mapping of Local Structure and CO<sub>2</sub> Adsorption in Metal-Organic Frameworks.

Journal of the American Chemical Society·2026
Same author

Diagnostic Yield of Comprehensive Reanalysis After Nondiagnostic Short-Read Genome Sequencing in Infants With Unexplained Epilepsy.

Neurology·2026
Same journal

OpenIMC: an open-source platform for analyzing single-cell and spatial proteomics by imaging mass cytometry.

BMC bioinformatics·2026
Same journal

NAP: an open source pipeline for cross-domain microbiome profiling using Nanopore sequencing-derived amplicon data.

BMC bioinformatics·2026
Same journal

SurvGME: an R package for survival analysis with graphical and measurement error models.

BMC bioinformatics·2026
Same journal

SimMapNet: a Bayesian framework for gene regulatory network inference using gene ontology similarities as external hint.

BMC bioinformatics·2026
Same journal

Dual channel drug-drug interactions extraction based on cross attention.

BMC bioinformatics·2026
Same journal

FeSseqdb: a curated sequence-level database and interpretable machine learning framework for identifying iron-sulfur proteins.

BMC bioinformatics·2026
See all related articles

Related Experiment Video

Updated: Apr 23, 2026

Targeted DNA Methylation Analysis by Next-generation Sequencing
08:38

Targeted DNA Methylation Analysis by Next-generation Sequencing

Published on: February 24, 2015

38.2K

A better sequence-read simulator program for metagenomics.

Stephen Johnson, Brett Trost, Jeffrey R Long

    BMC Bioinformatics
    |September 26, 2014
    PubMed
    Summary
    This summary is machine-generated.

    BEAR (Better Emulation for Artificial Reads) simulates metagenomic sequencing data with non-parametric distributions and quality profiles. This tool generates realistic reads for evaluating genomics data processing tools, especially for technologies like Ion Torrent.

    More Related Videos

    CIRCLE-Seq for Interrogation of Off-Target Gene Editing
    08:23

    CIRCLE-Seq for Interrogation of Off-Target Gene Editing

    Published on: November 1, 2024

    1.7K
    Metagenomic Analysis of Silage
    08:43

    Metagenomic Analysis of Silage

    Published on: January 13, 2017

    18.7K

    Related Experiment Videos

    Last Updated: Apr 23, 2026

    Targeted DNA Methylation Analysis by Next-generation Sequencing
    08:38

    Targeted DNA Methylation Analysis by Next-generation Sequencing

    Published on: February 24, 2015

    38.2K
    CIRCLE-Seq for Interrogation of Off-Target Gene Editing
    08:23

    CIRCLE-Seq for Interrogation of Off-Target Gene Editing

    Published on: November 1, 2024

    1.7K
    Metagenomic Analysis of Silage
    08:43

    Metagenomic Analysis of Silage

    Published on: January 13, 2017

    18.7K

    Area of Science:

    • Genomics
    • Bioinformatics
    • Computational Biology

    Background:

    • Existing whole-genome shotgun sequence simulators often use predefined models, limiting their applicability.
    • Current simulators are typically restricted to single-genome studies and do not support non-parametric read-length distributions or quality profiles derived from metagenomics data.

    Purpose of the Study:

    • To develop a novel program, BEAR (Better Emulation for Artificial Reads), for generating simulated metagenomic sequencing reads.
    • To enable the creation of simulated data that accurately reflects empirically-derived non-parametric read-length distributions and quality profiles from metagenomics datasets.

    Main Methods:

    • BEAR employs a machine-learning approach to emulate sequencing reads.
    • It automatically determines parameter settings from user-supplied data, requiring minimal input.
    • The program derives run-specific error rates and extracts quality-error models from metagenomic data.

    Main Results:

    • BEAR generates reads with lengths and quality values closely matching empirically-derived distributions.
    • It can emulate reads from various sequencing platforms, including Illumina, 454, and Ion Torrent, and is particularly useful for technologies lacking dedicated simulators, such as Ion Torrent.
    • BEAR automates the generation of abundance data, a previously arduous task in metagenomic simulation.

    Conclusions:

    • BEAR provides a significant advantage over existing software for evaluating genomics data processing tools.
    • Its ability to generate more realistic, technology-independent reads makes it highly valuable for metagenomics research.
    • The program's features streamline the simulation process, particularly for complex metagenomic datasets.