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

11.2K
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...
11.2K
Ribosome Profiling02:24

Ribosome Profiling

3.9K
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...
3.9K

You might also read

Related Articles

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

Sort by
Same author

Flexible and scalable inference of spatially varying correlation in spatial transcriptomics with spCorr.

Genome research·2026
Same author

CIPHER: An end-to-end framework for designing optimized aggregated spatial transcriptomics experiments.

PLoS computational biology·2026
Same author

IntegrateRigor: annotation-free integration optimization for cell identity recovery reveals cancer-immune interface niches.

bioRxiv : the preprint server for biology·2026
Same author

New proteomic biomarkers identified in plasma extracellular vesicles in sarcoidosis: a case-control matched study.

Frontiers in immunology·2026
Same author

SnakeAltPromoter Facilitates Differential Alternative Promoter Analysis.

Computational and structural biotechnology journal·2026
Same author

scDesignPop generates realistic population-scale single-cell RNA-seq for power analysis, benchmarking, and privacy protection.

bioRxiv : the preprint server for biology·2026
Same journal

Glycoform engineering of a mammalian platform to sculpt a humanized recombinant bioscavenger.

Cell systems·2026
Same journal

Targeted genomic editing of human gut Bacteroides species based on CRISPR-associated transposases.

Cell systems·2026
Same journal

Scalable enumeration and sampling of minimal metabolic pathways for organisms and communities.

Cell systems·2026
Same journal

Deciphering protein mutation-phenotype linkages from CRISPR-based tiling mutagenesis screens.

Cell systems·2026
Same journal

High-throughput machine learning-aided antibody discovery for cell surface antigens.

Cell systems·2026
Same journal

Quantitative cytokine profiling of primary human macrophages reveals distinct single-cell modes of trained immunity.

Cell systems·2026
See all related articles

Related Experiment Video

Updated: Nov 25, 2025

Single-cell RNA Sequencing and Analysis of Human Pancreatic Islets
11:34

Single-cell RNA Sequencing and Analysis of Human Pancreatic Islets

Published on: July 18, 2019

16.8K

Benchmarking Computational Doublet-Detection Methods for Single-Cell RNA Sequencing Data.

Nan Miles Xi1, Jingyi Jessica Li2

  • 1Department of Statistics, University of California, Los Angeles, CA 90095-1554, USA.

Cell Systems
|December 18, 2020
PubMed
Summary
This summary is machine-generated.

This study benchmarks computational doublet detection methods for single-cell RNA sequencing (scRNA-seq). DoubletFinder showed the best accuracy, while cxds was most efficient for scRNA-seq data analysis.

Keywords:
cell clusteringdifferential gene expressiondoublet detectionparallel computingreproducibilityscRNA-seqsoftware implementationtrajectory inference

More Related Videos

Real-time Analysis of Transcription Factor Binding, Transcription, Translation, and Turnover to Display Global Events During Cellular Activation
12:54

Real-time Analysis of Transcription Factor Binding, Transcription, Translation, and Turnover to Display Global Events During Cellular Activation

Published on: March 7, 2018

13.9K
Low-input Nucleus Isolation and Multiplexing with Barcoded Antibodies of Mouse Sympathetic Ganglia for Single-nucleus RNA Sequencing
10:44

Low-input Nucleus Isolation and Multiplexing with Barcoded Antibodies of Mouse Sympathetic Ganglia for Single-nucleus RNA Sequencing

Published on: March 23, 2022

4.6K

Related Experiment Videos

Last Updated: Nov 25, 2025

Single-cell RNA Sequencing and Analysis of Human Pancreatic Islets
11:34

Single-cell RNA Sequencing and Analysis of Human Pancreatic Islets

Published on: July 18, 2019

16.8K
Real-time Analysis of Transcription Factor Binding, Transcription, Translation, and Turnover to Display Global Events During Cellular Activation
12:54

Real-time Analysis of Transcription Factor Binding, Transcription, Translation, and Turnover to Display Global Events During Cellular Activation

Published on: March 7, 2018

13.9K
Low-input Nucleus Isolation and Multiplexing with Barcoded Antibodies of Mouse Sympathetic Ganglia for Single-nucleus RNA Sequencing
10:44

Low-input Nucleus Isolation and Multiplexing with Barcoded Antibodies of Mouse Sympathetic Ganglia for Single-nucleus RNA Sequencing

Published on: March 23, 2022

4.6K

Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Doublets, formed by two cells in one reaction, are a significant confounder in single-cell RNA sequencing (scRNA-seq) data.
  • The lack of comprehensive benchmarking for computational doublet detection methods hinders optimal scRNA-seq data analysis.

Purpose of the Study:

  • To systematically benchmark nine leading computational doublet detection methods for scRNA-seq data.
  • To evaluate method performance based on detection accuracy, impact on downstream analyses, and computational efficiency.

Main Methods:

  • Conducted a benchmark study using 16 real scRNA-seq datasets with experimentally annotated doublets.
  • Utilized 112 realistic synthetic scRNA-seq datasets to simulate various experimental conditions.
  • Compared nine computational doublet detection algorithms.

Main Results:

  • Existing doublet detection methods exhibit diverse performance and varying strengths.
  • DoubletFinder demonstrated superior detection accuracy across different experimental settings.
  • The cxds method achieved the highest computational efficiency among the evaluated tools.

Conclusions:

  • The choice of doublet detection method impacts scRNA-seq data analysis outcomes.
  • DoubletFinder is recommended for high detection accuracy, while cxds is suitable for computational efficiency.
  • This benchmark provides crucial guidance for researchers selecting doublet detection tools for scRNA-seq studies.