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Related Concept Videos

RNA-seq03:21

RNA-seq

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 microarray-based...
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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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Related Experiment Video

Updated: Jun 18, 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

mRNA-sequencing whole transcriptome analysis of a single cell on the SOLiD system.

Kai Q Lao1, Fuchou Tang, Catalin Barbacioru

  • 1Applied Biosystems, a division of Life Technologies Corporation, Genetic Analysis Business Unit, Foster City, California 94404, USA. kai.lao@lifetech.com

Journal of Biomolecular Techniques : JBT
|December 2, 2009
PubMed
Summary

This study introduces a new single-cell gene expression assay using SOLiD sequencing, revealing higher transcriptome complexity and abnormal transposon activity in knockout oocytes. This method enhances gene detection and transcript variant identification.

Keywords:
Ago2Dicergene expression

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Last Updated: Jun 18, 2026

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Multiplexed Single Cell mRNA Sequencing Analysis of Mouse Embryonic Cells

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Area of Science:

  • Genomics
  • Molecular Biology
  • Developmental Biology

Background:

  • Understanding gene expression at the single-cell level is crucial for developmental biology.
  • Existing methods have limitations in detecting the full spectrum of gene expression and transcript variants.

Purpose of the Study:

  • To develop and validate a novel sequencing-based assay for single-cell gene expression profiling.
  • To compare the sensitivity and scope of this new assay against traditional cDNA microarray techniques.
  • To investigate gene expression patterns in early embryonic blastomeres and in oocytes with disrupted RNA interference pathways.

Main Methods:

  • Development of a modified single-cell whole transcriptome amplification method.
  • Integration with the SOLiD (Sequencing by Oligonucleotide Ligation and Detection) next-generation sequencing system.
  • Application of the assay to four-cell stage blastomeres and Dicer/Ago2 knockout oocytes.

Main Results:

  • The assay demonstrated similar gene expression profiles in four-cell stage blastomeres, correlating with their developmental potential.
  • Compared to cDNA microarrays, the single-cell cDNA SOLiD sequencing assay detected thousands more genes.
  • Numerous novel transcript variants were identified, indicating greater transcriptome complexity than previously understood.
  • Significant upregulation of transposons was observed in Dicer/Ago2 knockout oocytes relative to wild-type controls.

Conclusions:

  • The developed assay provides unprecedented resolution for single-cell gene expression analysis.
  • The findings highlight the substantial complexity of the transcriptome and the importance of RNA interference pathways in maintaining genomic stability.
  • This technique offers a powerful tool for future research in developmental biology and gene regulation.