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
Next-generation Sequencing03:00

Next-generation Sequencing

99.3K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
99.3K
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

You might also read

Related Articles

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

Sort by
Same author

Capture, Confine, Characterize: High-Throughput Dielectrophoresis-Based Single-Cell Microfluidics Platform to Analyze Mammalian and Yeast Cells Using Raman Spectroscopy.

Small (Weinheim an der Bergstrasse, Germany)·2026
Same author

Capture, Confine, Characterize: High-Throughput Dielectrophoresis-Based Single-Cell Microfluidics Platform to Analyze Mammalian and Yeast Cells Using Raman Spectroscopy.

bioRxiv : the preprint server for biology·2025
Same author

SlideCNA: spatial copy number alteration detection from Slide-seq-like spatial transcriptomics data.

Genome biology·2025
Same author

Immune checkpoint TIM-3 regulates microglia and Alzheimer's disease.

Nature·2025
Same author

Author Correction: A multi-modal single-cell and spatial expression map of metastatic breast cancer biopsies across clinicopathological features.

Nature medicine·2025
Same author

Author Correction: B-cell-specific checkpoint molecules that regulate anti-tumour immunity.

Nature·2025
Same journal

RNAbpFlow: base pair-augmented SE(3) flow matching for conditional RNA 3D structure generation.

Nature methods·2026
Same journal

Spatio-DARLIN enables robust and efficient in situ lineage tracing in mice at single-cell resolution.

Nature methods·2026
Same journal

EasyGrid: a versatile platform for automated cryo-EM sample preparation and quality control.

Nature methods·2026
Same journal

Cloud-based microscope enables live neuroimaging for 24 h and beyond with worldwide access.

Nature methods·2026
Same journal

Deep molecular profiling in three dimensions.

Nature methods·2026
Same journal

3D pathology-guided microdissection.

Nature methods·2026
See all related articles

Related Experiment Video

Updated: Feb 24, 2026

Isolation of Adult Spinal Cord Nuclei for Massively Parallel Single-nucleus RNA Sequencing
06:38

Isolation of Adult Spinal Cord Nuclei for Massively Parallel Single-nucleus RNA Sequencing

Published on: October 12, 2018

19.8K

Massively parallel single-nucleus RNA-seq with DroNc-seq.

Naomi Habib1,2,3, Inbal Avraham-Davidi1, Anindita Basu1,4

  • 1Klarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.

Nature Methods
|August 29, 2017
PubMed
Summary
This summary is machine-generated.

We developed DroNc-seq, a high-throughput method for single-nucleus RNA sequencing, enabling efficient cell type classification from archived brain tissues. This technology advances the creation of comprehensive cell atlases.

More Related Videos

Pancreatic Tissue Dissection to Isolate Viable Single Cells
08:04

Pancreatic Tissue Dissection to Isolate Viable Single Cells

Published on: May 26, 2023

4.1K
An Ultrahigh-throughput Microfluidic Platform for Single-cell Genome Sequencing
10:00

An Ultrahigh-throughput Microfluidic Platform for Single-cell Genome Sequencing

Published on: May 23, 2018

18.4K

Related Experiment Videos

Last Updated: Feb 24, 2026

Isolation of Adult Spinal Cord Nuclei for Massively Parallel Single-nucleus RNA Sequencing
06:38

Isolation of Adult Spinal Cord Nuclei for Massively Parallel Single-nucleus RNA Sequencing

Published on: October 12, 2018

19.8K
Pancreatic Tissue Dissection to Isolate Viable Single Cells
08:04

Pancreatic Tissue Dissection to Isolate Viable Single Cells

Published on: May 26, 2023

4.1K
An Ultrahigh-throughput Microfluidic Platform for Single-cell Genome Sequencing
10:00

An Ultrahigh-throughput Microfluidic Platform for Single-cell Genome Sequencing

Published on: May 23, 2018

18.4K

Area of Science:

  • Genomics
  • Neuroscience
  • Biotechnology

Background:

  • Single-nucleus RNA sequencing (sNuc-seq) enables RNA profiling from preserved or difficult-to-dissociate tissues.
  • Current sNuc-seq methods lack high-throughput capabilities, limiting large-scale analyses.
  • Archived human and mouse brain samples are valuable resources for cellular and molecular studies.

Purpose of the Study:

  • To develop a massively parallel single-nucleus RNA sequencing method.
  • To enable high-throughput profiling of nuclei from archived tissues.
  • To demonstrate the utility of this method for cell type classification and atlas generation.

Main Methods:

  • Development of DroNc-seq, integrating droplet technology with sNuc-seq.
  • Profiling of 39,111 nuclei from archived mouse and human brain samples.
  • Application of sensitive, efficient, and unbiased cell type classification algorithms.

Main Results:

  • DroNc-seq achieves massively parallel single-nucleus RNA sequencing.
  • Sensitive, efficient, and unbiased classification of cell types was demonstrated.
  • Successful profiling of 39,111 nuclei from archived brain samples.

Conclusions:

  • DroNc-seq significantly enhances the throughput of sNuc-seq.
  • This method facilitates systematic charting of cell atlases from archived tissues.
  • DroNc-seq is a powerful tool for large-scale neuroscience research.