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Related Concept Videos

RNA-seq03:21

RNA-seq

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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...
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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.
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Updated: Oct 2, 2025

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

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Single Cell RNA Sequencing in NASH.

Jana Hundertmark1, Hilmar Berger1, Frank Tacke2

  • 1Department of Hepatology and Gastroenterology, Charité-Universitätsmedizin Berlin, Berlin, Germany.

Methods in Molecular Biology (Clifton, N.J.)
|February 25, 2022
PubMed
Summary
This summary is machine-generated.

Single cell RNA sequencing (scRNA-seq) reveals diverse liver myeloid cells in non-alcoholic steatohepatitis (NASH). This method aids in understanding macrophage roles in fatty liver disease progression.

Keywords:
10× GenomicsFibrosisMacrophagesMyeloid immune cellsNAFLDNASHSingle cell RNA sequencing (scRNA-seq)Transcriptomics

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Area of Science:

  • Immunology
  • Genomics
  • Hepatology

Background:

  • Non-alcoholic steatohepatitis (NASH) involves complex liver inflammation.
  • Myeloid cells, especially macrophages, are key drivers of NASH progression.
  • Analyzing myeloid cell heterogeneity is crucial for understanding liver disease.

Purpose of the Study:

  • To apply microdroplet-based single-cell RNA sequencing (scRNA-seq) to mouse liver myeloid cells.
  • To identify and characterize distinct hepatic macrophage populations in NASH.
  • To analyze gene expression differences between healthy and NASH liver myeloid cells.

Main Methods:

  • Isolation of myeloid cell populations from mouse liver.
  • Microdroplet-based single-cell RNA sequencing (scRNA-seq) for high-throughput analysis.
  • Differential gene expression analysis between healthy and NASH samples.

Main Results:

  • Successful isolation and scRNA-seq analysis of liver myeloid cells.
  • Identification and characterization of specific hepatic macrophage subpopulations.
  • Discovery of differentially expressed genes associated with NASH.

Conclusions:

  • scRNA-seq is effective for dissecting myeloid cell heterogeneity in the liver.
  • This approach enhances understanding of macrophage roles in NASH pathogenesis.
  • The findings provide a basis for further research into NASH-associated myeloid cell functions.