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

10.5K
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...
10.5K
Ribosome Profiling02:24

Ribosome Profiling

3.7K
Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
3.7K

You might also read

Related Articles

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

Sort by
Same author

A histidine switch controls the pH-responsive self-assembly of a helical protein filament.

bioRxiv : the preprint server for biology·2026
Same author

Structural basis of membrane potential coupled vectorial CO₂ hydration by the DAB2 complex in chemolithoautotrophs.

Nature communications·2026
Same author

Cryo-EM structure of locked spike glycoprotein from bat SARS-like coronavirus WIV1, molecular dynamics and biophysics across host range.

Proceedings of the National Academy of Sciences of the United States of America·2026
Same author

Structure of the Methanosarcina mazei Mtr complex bound to the oxygen-stress responsive small protein MtrI.

Nature communications·2025
Same author

A histidine switch regulates pH-dependent filament formation by the caspase-9 CARD.

bioRxiv : the preprint server for biology·2025
Same author

The Mediator Kinase Module regulates cell cycle re-entry and transcriptional responses following DNA damage.

bioRxiv : the preprint server for biology·2025
Same journal

Editorial: Technologies for RNA Detection.

Bio-protocol·2026
Same journal

One-Step Affinity Purification of MarathonRT Reverse Transcriptase for RNA Sequencing Applications.

Bio-protocol·2026
Same journal

Enhanced RNA-Seq Expression Profiling and Functional Enrichment in Non-model Organisms Using Custom Annotations.

Bio-protocol·2026
Same journal

Using Combined Fluorescent In Situ Hybridization With Immunohistochemistry to Co-localize mRNA in Diverse Neuronal Cell Types.

Bio-protocol·2026
Same journal

Stepwise Protocol for Alternative Splicing Analysis in Single-Cell SMART-Seq2 RNA-Seq Data.

Bio-protocol·2026
Same journal

Enriching Bacteria-Specific RNA From Host Samples Before NGS With Transcript-Capture.

Bio-protocol·2026
See all related articles

Related Experiment Video

Updated: Oct 15, 2025

Measuring mRNA Levels Over Time During the Yeast S. cerevisiae Hypoxic Response
09:45

Measuring mRNA Levels Over Time During the Yeast S. cerevisiae Hypoxic Response

Published on: August 10, 2017

8.4K

Protocol for RNA-seq Expression Analysis in Yeast.

Stefan Bohn1

  • 1Institute of Structural Biology, Helmholtz Zentrum München, Munich, Germany.

Bio-Protocol
|October 25, 2021
PubMed
Summary
This summary is machine-generated.

This study details the RNA sequencing (RNA-seq) workflow for gene expression analysis in yeast. It simplifies the complex data processing steps, making RNA-seq more accessible for researchers.

Keywords:
Next-generation sequencingRelative expression levelsSequence analysisSystems biologyWhole genomeYeastmRNA

More Related Videos

Genome-wide Quantification of Translation in Budding Yeast by Ribosome Profiling
12:57

Genome-wide Quantification of Translation in Budding Yeast by Ribosome Profiling

Published on: December 21, 2017

11.6K
Saccharomyces cerevisiae Metabolic Labeling with 4-thiouracil and the Quantification of Newly Synthesized mRNA As a Proxy for RNA Polymerase II Activity
09:21

Saccharomyces cerevisiae Metabolic Labeling with 4-thiouracil and the Quantification of Newly Synthesized mRNA As a Proxy for RNA Polymerase II Activity

Published on: October 22, 2018

9.3K

Related Experiment Videos

Last Updated: Oct 15, 2025

Measuring mRNA Levels Over Time During the Yeast S. cerevisiae Hypoxic Response
09:45

Measuring mRNA Levels Over Time During the Yeast S. cerevisiae Hypoxic Response

Published on: August 10, 2017

8.4K
Genome-wide Quantification of Translation in Budding Yeast by Ribosome Profiling
12:57

Genome-wide Quantification of Translation in Budding Yeast by Ribosome Profiling

Published on: December 21, 2017

11.6K
Saccharomyces cerevisiae Metabolic Labeling with 4-thiouracil and the Quantification of Newly Synthesized mRNA As a Proxy for RNA Polymerase II Activity
09:21

Saccharomyces cerevisiae Metabolic Labeling with 4-thiouracil and the Quantification of Newly Synthesized mRNA As a Proxy for RNA Polymerase II Activity

Published on: October 22, 2018

9.3K

Area of Science:

  • Molecular Biology
  • Genomics
  • Bioinformatics

Background:

  • Genome-wide sequencing of RNA (RNA-seq) offers valuable insights into cellular and disease mechanisms.
  • RNA-seq sample preparation and sequencing are efficient, yielding numerous gene expression profiles rapidly.
  • However, the subsequent data processing, curation, and analysis present significant challenges for non-experts.

Purpose of the Study:

  • To describe a streamlined workflow for RNA-seq expression analysis in yeast.
  • To demystify the data processing, curation, and analysis stages of RNA-seq experiments.
  • To provide a foundational protocol adaptable for various RNA-seq applications.

Main Methods:

  • Detailed protocol for sample preparation for RNA-seq.
  • Description of the sequencing process for gene expression profiling.
  • Step-by-step guide to RNA-seq data processing and analysis.

Main Results:

  • A comprehensive workflow for yeast RNA-seq expression analysis is presented.
  • The protocol simplifies complex bioinformatics steps, enhancing accessibility.
  • The described workflow serves as a adaptable foundation for diverse RNA-seq studies.

Conclusions:

  • This protocol facilitates the application of RNA-seq for gene expression analysis, particularly for non-experts.
  • The described workflow enhances the understanding and implementation of RNA-seq data analysis.
  • The study provides a valuable resource for researchers utilizing RNA-seq in yeast and beyond.