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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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Isolating, Sequencing and Analyzing Extracellular MicroRNAs from Human Mesenchymal Stem Cells
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Cell-Free RNA Sequencing from Biofluid Samples.

Lili Zhang1, Xingyu Liu1, Chen Wang1

  • 1Genesis, Beijing, China.

Methods in Molecular Biology (Clifton, N.J.)
|July 14, 2023
PubMed
Summary
This summary is machine-generated.

This study presents an optimized protocol for detecting cell-free RNA (cfRNA) using next-generation sequencing (NGS). This method enhances the potential of cfRNA as a promising biomarker for disease detection, even with limited sample amounts.

Keywords:
Liquid biopsyLow-abundant RNA library constructioncfRNA biomarkerscfRNA sequencing

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Area of Science:

  • Biomolecular analysis
  • Molecular diagnostics

Background:

  • Liquid biopsies offer advantages over invasive procedures.
  • Cell-free DNA (cfDNA) is established in diagnostics.
  • Cell-free RNA (cfRNA) shows diagnostic potential despite instability.

Purpose of the Study:

  • To introduce a modified protocol for cfRNA detection.
  • To optimize next-generation sequencing (NGS) for cfRNA analysis.
  • To enable cfRNA detection from low-input, fragmented samples.

Main Methods:

  • Development of a modified cfRNA detection protocol.
  • Application of next-generation sequencing (NGS) technology.
  • Optimization for handling low-input and fragmented cfRNA.

Main Results:

  • A functional protocol for cfRNA detection via NGS was established.
  • The protocol is optimized for challenging cfRNA sample types.
  • Demonstrated feasibility of cfRNA analysis with limited starting material.

Conclusions:

  • The modified NGS protocol facilitates cfRNA detection.
  • This approach supports the development of cfRNA-based diagnostic assays.
  • Optimized cfRNA analysis holds promise for future disease detection strategies.