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

10.3K
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...
10.3K
Ribosome Profiling02:24

Ribosome Profiling

3.6K
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...
3.6K

You might also read

Related Articles

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

Sort by
Same author

CircZBTB46, a promising therapeutic target in crizotinib resistant ALK-positive T lymphomas.

Leukemia·2026
Same author

CircRNAs derived from the tyrosine phosphatase PTPN22 impact chemosensitivity in ALK-positive T-cell lymphomas.

Scientific reports·2026
Same author

High-quality chromosome-scale genome assemblies of 29 maize inbred lines of European breeding relevance.

Scientific data·2026
Same author

Comprehensive detection of structural variations in long and short reads dataset of French cattle.

Scientific reports·2025
Same author

Application of a French cattle pangenome, from structural variant discovery to association studies on key phenotypes.

Genetics, selection, evolution : GSE·2025
Same author

Whole genome short read data from 567 bulls of 14 breeds provides insight into genetic diversity of French cattle.

Data in brief·2025
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: Aug 20, 2025

Mapping RNA-RNA Interactions Globally Using Biotinylated Psoralen
11:32

Mapping RNA-RNA Interactions Globally Using Biotinylated Psoralen

Published on: May 24, 2017

12.2K

srnaMapper: an optimal mapping tool for sRNA-Seq reads.

Matthias Zytnicki1, Christine Gaspin2

  • 1Unité de Mathématiques et Informatique Appliquées, INRAE, Castanet-Tolosan, France. matthias.zytnicki@inrae.fr.

BMC Bioinformatics
|November 19, 2022
PubMed
Summary
This summary is machine-generated.

A new tool, srnaMapper, efficiently maps short RNA sequencing reads, addressing unique features like redundancy and end editing. It accurately retrieves all genomic hits, even with errors, in competitive computation times.

Keywords:
MappingSRNASequencing

More Related Videos

Identification of Alternative Splicing and Polyadenylation in RNA-seq Data
08:35

Identification of Alternative Splicing and Polyadenylation in RNA-seq Data

Published on: June 24, 2021

5.7K
MS2-Affinity Purification Coupled with RNA Sequencing in Gram-Positive Bacteria
08:34

MS2-Affinity Purification Coupled with RNA Sequencing in Gram-Positive Bacteria

Published on: February 23, 2021

6.9K

Related Experiment Videos

Last Updated: Aug 20, 2025

Mapping RNA-RNA Interactions Globally Using Biotinylated Psoralen
11:32

Mapping RNA-RNA Interactions Globally Using Biotinylated Psoralen

Published on: May 24, 2017

12.2K
Identification of Alternative Splicing and Polyadenylation in RNA-seq Data
08:35

Identification of Alternative Splicing and Polyadenylation in RNA-seq Data

Published on: June 24, 2021

5.7K
MS2-Affinity Purification Coupled with RNA Sequencing in Gram-Positive Bacteria
08:34

MS2-Affinity Purification Coupled with RNA Sequencing in Gram-Positive Bacteria

Published on: February 23, 2021

6.9K

Area of Science:

  • Genomics
  • Bioinformatics
  • Molecular Biology

Background:

  • Short RNA sequencing (including microRNAs, tRNA-derived RNAs, and piwi-interacting RNAs) is crucial for biological studies.
  • Mapping sequencing reads to a genome is the essential first step for analyzing short RNAs.
  • Existing mapping tools are designed for long RNAs and do not account for the unique characteristics of short RNAs.

Purpose of the Study:

  • To develop a novel bioinformatics tool, srnaMapper, specifically designed for the exhaustive mapping of short RNA sequencing reads.
  • To address the distinct features of short RNAs, such as their short length, redundancy, duplicated loci origins, and end editing.

Main Methods:

  • Development of srnaMapper, a tool optimized for reads up to 50 base pairs.
  • Exhaustive mapping approach considering short RNA specificities.
  • Evaluation of computational efficiency and error handling capabilities.

Main Results:

  • srnaMapper demonstrates high efficiency in terms of computation time.
  • The tool effectively handles sequencing errors and end editing.
  • It retrieves all possible genomic hits, even with a specified number of errors.
  • Performance is comparable to non-exhaustive mapping tools.

Conclusions:

  • srnaMapper provides an efficient and accurate solution for mapping short RNA sequencing data.
  • The tool's design accounts for the unique challenges posed by short RNA analysis.
  • It offers a significant improvement over existing methods for short RNA read mapping.