Related Experiment Video

Updated: Feb 24, 2026

Multiplexed Single Cell mRNA Sequencing Analysis of Mouse Embryonic Cells
08:30

Multiplexed Single Cell mRNA Sequencing Analysis of Mouse Embryonic Cells

Published on: January 7, 2020

14.0K

New skin for the old RNA-Seq ceremony: the age of single-cell multi-omics

Maayan Baron1, Itai Yanai2

  • 1Institute for Computational Medicine, NYU School of Medicine, 430 East 29th St., New York, NY, 10016, USA.

Genome Biology
|August 25, 2017
PubMed

Abstract:

New methods for simultaneously quantifying protein and gene expression at the single-cell level have the power to identify cell types and to classify cell populations.

More Related Videos

Droplet Barcoding-Based Single Cell Transcriptomics of Adult Mammalian Tissues
10:12

Droplet Barcoding-Based Single Cell Transcriptomics of Adult Mammalian Tissues

Published on: January 10, 2019

19.2K
Multiplexed Analysis of Retinal Gene Expression and Chromatin Accessibility Using scRNA-Seq and scATAC-Seq
06:24

Multiplexed Analysis of Retinal Gene Expression and Chromatin Accessibility Using scRNA-Seq and scATAC-Seq

Published on: March 12, 2021

4.2K

Related Experiment Videos

Last Updated: Feb 24, 2026

Multiplexed Single Cell mRNA Sequencing Analysis of Mouse Embryonic Cells
08:30

Multiplexed Single Cell mRNA Sequencing Analysis of Mouse Embryonic Cells

Published on: January 7, 2020

14.0K
Droplet Barcoding-Based Single Cell Transcriptomics of Adult Mammalian Tissues
10:12

Droplet Barcoding-Based Single Cell Transcriptomics of Adult Mammalian Tissues

Published on: January 10, 2019

19.2K
Multiplexed Analysis of Retinal Gene Expression and Chromatin Accessibility Using scRNA-Seq and scATAC-Seq
06:24

Multiplexed Analysis of Retinal Gene Expression and Chromatin Accessibility Using scRNA-Seq and scATAC-Seq

Published on: March 12, 2021

4.2K

Related Concept Videos

RNA-seq03:21

RNA-seq

12.2K
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...
12.2K
Ribosome Profiling02:24

Ribosome Profiling

4.2K
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...
4.2K

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

Melanoma evolution in the lymph node shapes systemic outcomes.

bioRxiv : the preprint server for biology·2026

A mechanism for adaptive genome regulation in cancer.

Nature·2026

Cross-species analysis identifies genotype-driven vulnerabilities in lung adenocarcinoma.

bioRxiv : the preprint server for biology·2025

Dissecting microbial communities with single-cell transcriptome analysis.

Science (New York, N.Y.)·2025

Mechanical confinement governs phenotypic plasticity in melanoma.

Nature·2025

Desmosome mutations impact the tumor microenvironment to promote melanoma proliferation.

Nature genetics·2025

dicast: a machine learning method for accurate structural variant detection from short-read sequencing data.

Genome biology·2026

Decoding the cancer microbiome: multi-omics, AI, and translational opportunities.

Genome biology·2026

Genolator enables protein function interpretation using a multimodal large language model fusing genomic and structural interpretation with natural language interaction.

Genome biology·2026

Population genomics, demography, and circum-Baltic connectivity of Early Medieval southwestern Finland.

Genome biology·2026

COSIGT: population-scalable genotyping of complex loci from low-coverage sequencing data using pangenome graphs.

Genome biology·2026

Large-scale benchmarking of prokaryotic annotation tools across thousands of species.

Genome biology·2026

Identification of Variants in Two Families With Congenital Cataract by Whole Exome Sequencing.

Molecular genetics & genomic medicine·2026

Golgi dysfunction in Alzheimer disease: from human multiomic signatures to therapeutic targets.

Experimental & molecular medicine·2026

Current translational perspectives for diagnosis and individualized therapy in rare genetic diseases.

Communications medicine·2026

NEDD9 inhibits ox-LDL-induced endothelial anoikis to attenuate endothelial cell injury.

Cellular signalling·2026

Genome-wide transcriptomics and a machine learning-based random forest model identify novel biomarkers to predict phenotypic variability in Wilson disease.

Human immunology·2026

Sex hormone-binding globulin increases lumbar fracture risk via bone density, inflammation, and insulin pathways: A Mendelian randomization study.

Medicine·2026
See all related articles
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
Jove
Visualize
Contact Us