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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. 
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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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Related Experiment Video

Updated: May 6, 2026

A Droplet-Based Microfluidic Approach and Microsphere-PCR Amplification for Single-Stranded DNA Amplicons
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A Droplet-Based Microfluidic Approach and Microsphere-PCR Amplification for Single-Stranded DNA Amplicons

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DNA sequence analysis with droplet-based microfluidics.

Adam R Abate1, Tony Hung, Ralph A Sperling

  • 1University of California, San Francisco - Bioengineering and Therapeutic Sciences, San Francisco, California, USA.

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|November 5, 2013
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Summary
This summary is machine-generated.

Droplet microfluidics enables rapid DNA sequencing using fluorescence resonance energy transfer (FRET) probes. This method efficiently identifies genetic variations in individual DNA molecules.

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Area of Science:

  • Biochemistry
  • Molecular Biology
  • Microfluidics

Background:

  • Droplet-based microfluidics allows high-throughput biochemical reactions in discrete compartments.
  • This technology has applications in enzyme engineering, DNA quantification, and protein crystallization screening.

Purpose of the Study:

  • To develop a droplet microfluidic method for DNA sequence reading.
  • To utilize a Förster Resonance Energy Transfer (FRET)-based assay for DNA polymorphism detection.

Main Methods:

  • Employing droplet microfluidics to encapsulate individual DNA molecules.
  • Designing sequence-specific probes for FRET-based interrogation of target DNA.
  • Analyzing FRET signals to identify polymorphisms in DNA sequences.

Main Results:

  • Demonstrated the ability to read DNA sequences using droplet microfluidics and FRET assays.
  • Successfully identified polymorphisms in target DNA molecules using specifically designed probes.
  • Showcased the potential for interrogating multiple polymorphisms and arbitrary DNA sequences.

Conclusions:

  • Droplet microfluidics combined with FRET assays provides a powerful platform for high-throughput DNA sequencing and polymorphism analysis.
  • This approach offers a versatile tool for genetic variation studies with potential for scalability.