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

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

You might also read

Related Articles

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

Sort by
Same author

HuBMAP Data Portal: A Resource for Multimodal Spatial and Single-Cell Data of Healthy Human Tissues.

ArXiv·2026
Same author

NKG2C <sup>+</sup> CD27 <sup>-</sup> Defines Human CD8 <sup>+</sup> Regulatory T Cells.

bioRxiv : the preprint server for biology·2026
Same author

Editorial: AI in single-cell biology.

Frontiers in bioinformatics·2026
Same author

NOD2 activation reprograms infiltrating inflammatory monocytes in the Zika virus infected CNS to maintain neural correlates of learning and memory.

bioRxiv : the preprint server for biology·2026
Same author

SpatialQuery: scalable discovery and molecular characterization of multicellular motifs from spatial omics data.

bioRxiv : the preprint server for biology·2026
Same author

Integration of large, complex single-cell datasets with Harmony2.

bioRxiv : the preprint server for biology·2026
Same journal

Toward molecular and pathology-confirmed completeness in advanced ovarian cancer cytoreduction: Intraoperative molecular imaging and integrated theranostic strategies.

Molecular aspects of medicine·2026
Same journal

Gut microbiota dysbiosis in chronic liver disease: Mechanisms driving hepatocellular carcinoma progression and therapeutic implications of Chinese medicine.

Molecular aspects of medicine·2026
Same journal

Mechanisms of resistance to androgen deprivation therapy in prostate cancer.

Molecular aspects of medicine·2026
Same journal

Extracellular vesicles and their cargo molecules for peripheral nerve injuries and neuropathies: The composition, properties, and impact.

Molecular aspects of medicine·2026
Same journal

Unravelling the mystery of hypoxia-induced miRNAs in breast cancer: A molecular cross-talk driving tumour progression and therapy resistance.

Molecular aspects of medicine·2026
Same journal

Decoding the dialogue: The vagus nerve at the interface of brain, body, and Tumor.

Molecular aspects of medicine·2026
See all related articles

Related Experiment Video

Updated: Feb 26, 2026

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

Identifying cell populations with scRNASeq.

Tallulah S Andrews1, Martin Hemberg1

  • 1Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire, UK.

Molecular Aspects of Medicine
|July 18, 2017
PubMed
Summary
This summary is machine-generated.

Single-cell RNA sequencing (scRNA-seq) offers powerful transcriptome analysis but presents computational challenges. This study reviews methods for gene identification, data dimensionality reduction, and cell population clustering to aid interpretation.

More Related Videos

Single-cell RNA-Seq of Defined Subsets of Retinal Ganglion Cells
11:26

Single-cell RNA-Seq of Defined Subsets of Retinal Ganglion Cells

Published on: May 22, 2017

14.4K
Isolation of Region-specific Microglia from One Adult Mouse Brain Hemisphere for Deep Single-cell RNA Sequencing
09:49

Isolation of Region-specific Microglia from One Adult Mouse Brain Hemisphere for Deep Single-cell RNA Sequencing

Published on: December 3, 2019

11.7K

Related Experiment Videos

Last Updated: Feb 26, 2026

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
Single-cell RNA-Seq of Defined Subsets of Retinal Ganglion Cells
11:26

Single-cell RNA-Seq of Defined Subsets of Retinal Ganglion Cells

Published on: May 22, 2017

14.4K
Isolation of Region-specific Microglia from One Adult Mouse Brain Hemisphere for Deep Single-cell RNA Sequencing
09:49

Isolation of Region-specific Microglia from One Adult Mouse Brain Hemisphere for Deep Single-cell RNA Sequencing

Published on: December 3, 2019

11.7K

Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Single-cell RNA sequencing (scRNA-seq) enables high-resolution transcriptome quantification.
  • scRNA-seq data is characterized by high dimensionality and noise, complicating analysis.
  • Effective computational strategies are crucial for extracting biological insights from scRNA-seq data.

Purpose of the Study:

  • To provide an overview of experimental protocols for scRNA-seq.
  • To present popular computational methods for scRNA-seq data analysis.
  • To guide researchers in interpreting cell types and states.

Main Methods:

  • Overview of experimental protocols.
  • Review of computational approaches for gene identification.
  • Discussion of dimensionality reduction techniques.
  • Exploration of clustering methods for cell population discovery.
  • Examination of validation and interpretation strategies.

Main Results:

  • Identification of key computational methods for scRNA-seq analysis.
  • Demonstration of approaches for reducing data dimensionality.
  • Presentation of clustering techniques for cell population delineation.
  • Guidance on validating and interpreting biological findings.

Conclusions:

  • Computational analysis of scRNA-seq data requires specialized methods.
  • Effective gene identification, dimensionality reduction, and clustering are essential.
  • Robust validation and interpretation are critical for biological discovery.