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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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Next-generation Sequencing03:00

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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.
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Sanger Sequencing01:57

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DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
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Updated: Oct 13, 2025

Droplet Barcoding-Based Single Cell Transcriptomics of Adult Mammalian Tissues
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From bulk, single-cell to spatial RNA sequencing.

Xinmin Li1, Cun-Yu Wang2,3

  • 1UCLA Technology Center for Genomics & Bioinformatics, Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA. xinminli@mednet.ucla.edu.

International Journal of Oral Science
|November 16, 2021
PubMed
Summary
This summary is machine-generated.

RNA sequencing technologies, including bulk, single-cell, and spatial RNAseq, offer comprehensive genetic insights beyond DNA sequencing. These advancements are crucial for understanding gene expression and driving precision oncology.

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Area of Science:

  • Genomics
  • Molecular Biology
  • Bioinformatics

Background:

  • RNA sequencing (RNAseq) provides a comprehensive genetic profile, detecting gene fusions, splicing variants, and mutations, surpassing DNA sequencing.
  • RNA sequencing has evolved from bulk RNAseq to single-cell RNA sequencing (scRNAseq) and spatial RNA sequencing (spRNAseq).

Purpose of the Study:

  • To highlight the evolution and characteristic features of different RNA sequencing technologies.
  • To discuss the suitable applications of these RNA sequencing methods in precision oncology.

Main Methods:

  • Review of bulk RNA sequencing for average global gene expression analysis.
  • Overview of single-cell RNA sequencing (scRNAseq) for analyzing individual cell RNA biology.
  • Introduction to spatial RNA sequencing (spRNAseq) for dissecting RNA activities within their spatial context.

Main Results:

  • RNA sequencing offers a more complete genetic picture than DNA sequencing by revealing gene fusions, splicing variants, and mutations.
  • Each RNA sequencing type (bulk, scRNAseq, spRNAseq) provides distinct advantages for different research questions.
  • Spatial RNA sequencing represents a significant advancement, enabling spatially resolved transcriptomic analysis.

Conclusions:

  • RNA sequencing technologies are indispensable tools in modern genomics.
  • The diverse applications of RNA sequencing, particularly in precision oncology, are expanding.
  • Spatial RNA sequencing is poised to become a cornerstone of next-generation molecular profiling.