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Related Concept Videos

Sanger Sequencing01:57

Sanger Sequencing

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...
Next-generation Sequencing03:00

Next-generation Sequencing

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.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.

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Related Experiment Video

Updated: Jun 9, 2026

Sequencing of mRNA from Whole Blood using Nanopore Sequencing
11:26

Sequencing of mRNA from Whole Blood using Nanopore Sequencing

Published on: June 3, 2019

Nanopore DNA sequencing with MspA.

Ian M Derrington1, Tom Z Butler, Marcus D Collins

  • 1Department of Physics, University of Washington, Seattle, WA 98195-1560, USA.

Proceedings of the National Academy of Sciences of the United States of America
|August 28, 2010
PubMed
Summary
This summary is machine-generated.

This study shows that the Mycobacterium smegmatis porin A (MspA) nanopore can distinguish individual DNA nucleotides. This demonstrates a simple, fast, and inexpensive DNA sequencing method using nanopore technology.

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Last Updated: Jun 9, 2026

Sequencing of mRNA from Whole Blood using Nanopore Sequencing
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Published on: March 15, 2019

Area of Science:

  • Biotechnology
  • Genomics
  • Molecular Biology

Background:

  • Nanopore sequencing offers a promising approach for rapid and cost-effective DNA analysis.
  • Current nanopore sequencing methods rely on detecting ionic current changes as DNA passes through a pore.

Purpose of the Study:

  • To investigate the potential of Mycobacterium smegmatis porin A (MspA) as a nanopore for DNA sequencing.
  • To demonstrate the ability of MspA to differentiate individual DNA nucleotides.

Main Methods:

  • Utilizing an engineered MspA nanopore to analyze single-stranded DNA.
  • Measuring ionic current modulation as DNA nucleotides pass through the MspA pore constriction.
  • Employing double-stranded DNA segments to temporarily position nucleotides within the pore.

Main Results:

  • The MspA nanopore successfully distinguished between all four DNA nucleotides.
  • Single-nucleotide resolution was achieved for single-stranded DNA.
  • Proof of principle for a simplified nanopore DNA sequencing method was established.

Conclusions:

  • MspA exhibits the capability to serve as a functional nanopore for DNA sequencing.
  • The MspA nanopore is a significant development for advancing nanopore sequencing technologies.
  • This research highlights MspA's potential impact on the future of rapid and affordable DNA sequencing.