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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...
10.3K

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Live-Cell Imaging of Transcriptional Activity at DNA Double-Strand Breaks
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Live-seq enables temporal transcriptomic recording of single cells.

Wanze Chen1,2,3, Orane Guillaume-Gentil4, Pernille Yde Rainer1,2

  • 1Laboratory of Systems Biology and Genetics, Institute of Bio-engineering and Global Health Institute, School of Life Sciences, Swiss Federal Institute of Technology (EPFL), Lausanne, Switzerland.

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|August 17, 2022
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Summary

Live-seq enables single-cell transcriptome profiling while preserving cell viability. This innovative method allows tracking cellular behavior over time, transforming single-cell RNA sequencing into a temporal analysis approach.

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Last Updated: Sep 1, 2025

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Live Imaging Followed by Single Cell Tracking to Monitor Cell Biology and the Lineage Progression of Multiple Neural Populations
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Area of Science:

  • Molecular Biology
  • Genomics
  • Cell Biology

Background:

  • Single-cell RNA sequencing (scRNA-seq) is crucial for understanding cellular heterogeneity.
  • Current scRNA-seq methods lyse cells, preventing subsequent analyses on the same cells.

Purpose of the Study:

  • To develop a single-cell transcriptome profiling method that preserves cell viability.
  • To enable coupling of a cell's transcriptome with its downstream molecular and phenotypic behavior.

Main Methods:

  • Live-seq utilizes fluidic force microscopy for RNA extraction, maintaining cell viability.
  • Benchmarking involved assessing cell growth, functional responses, and transcriptome readouts.
  • Proof-of-concept studies included sequential profiling of macrophages and adipose stromal cells, and transcriptomic recording.

Main Results:

  • Live-seq accurately stratifies diverse cell types and states with minimal cellular perturbation.
  • Demonstrated sequential mapping of macrophage and adipose stromal cell trajectories post-stimulation/differentiation.
  • Identified basal Nfkbia expression and cell cycle state as key determinants of macrophage LPS response heterogeneity.

Conclusions:

  • Live-seq transforms scRNA-seq from an endpoint analysis to a temporal analysis approach.
  • This method allows for direct coupling of transcriptome data with downstream cellular behavior.
  • Live-seq opens new avenues for studying dynamic cellular processes and responses.