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Low-cost, ultra-fast DNA sequencing brings diagnostic use closer

May 22, 2010
Boston University College of Engineering
Researchers show the viability of a novel, more efficient method to sequence DNA using nanopores. By doing it fast and inexpensively, this method brings routine use of DNA sequencing in medical diagnostics closer to reality.

Sequencing DNA could get a lot faster and cheaper -- and thus closer to routine use in clinical diagnostics -- thanks to a new method developed by a research team based at Boston University. The team has demonstrated the first use of solid state nanopores -- tiny holes in silicon chips that detect DNA molecules as they pass through the pore -- to read the identity of the four nucleotides that encode each DNA molecule. In addition, the researchers have shown the viability of a novel, more efficient method to detect single DNA molecules in nanopores.

"We have employed, for the first time, an optically-based method for DNA sequence readout combined with the nanopore system," said Boston University biomedical engineer Amit Meller, who collaborated with other researchers at Boston University, and at the University of Massachusetts Medical School in Worcester. "This allows us to probe multiple pores simultaneously using a single fast digital camera. Thus our method can be scaled up vastly, allowing us to obtain unprecedented DNA sequencing throughput."

The research is detailed in Nano Letters. The National Institutes of Health are currently considering a four-year grant application to further advance Meller's nanopore sequencing project.

This low-cost, ultra-fast DNA sequencing could revolutionize both healthcare and biomedical research, and lead to major advances in drug development, preventative medicine and personalized medicine. By gaining access to the entire sequence of a patient's genome, a physician could determine the probability of that patient developing a specific genetic disease.

The team's findings show that nanopores, which can analyze extremely long DNA molecules with superior precision, are uniquely positioned to compete with current, third-generation DNA sequencing methods for cost, speed and accuracy. Unlike those approaches, the new nanopore method does not rely on enzymes whose activity limits the rate at which DNA sequences can be read.

"This puts us in the unique advantageous position of being able to claim that our sequencing method is as fast as the rapidly evolving photographic technologies," said Meller. "We currently have the capability of reading out about 200 bases per second, which is already much faster than other commercial third-generation methods. This is only the starting point for us, and we expect to increase this rate by up to a factor of four in the next year." Licensing intellectual property from Boston University and Harvard University, Meller and his collaborators recently founded NobleGen Biosciences to develop and commercialize nanopore sequencing based on the new method.

"I believe that it will take three to five years to bring cheap DNA sequencing to the medical marketplace, assuming an aggressive research and development program is in place," said Meller.

Story Source:

The above post is reprinted from materials provided by Boston University College of Engineering. Note: Materials may be edited for content and length.

Journal Reference:

  1. Ben McNally, Alon Singer, Zhiliang Yu, Yingjie Sun, Zhiping Weng, Amit Meller. Optical Recognition of Converted DNA Nucleotides for Single-Molecule DNA Sequencing Using Nanopore Arrays. Nano Letters, 2010; 100511092117086 DOI: 10.1021/nl1012147

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Boston University College of Engineering. "Low-cost, ultra-fast DNA sequencing brings diagnostic use closer." ScienceDaily. ScienceDaily, 22 May 2010. <>.
Boston University College of Engineering. (2010, May 22). Low-cost, ultra-fast DNA sequencing brings diagnostic use closer. ScienceDaily. Retrieved December 1, 2015 from
Boston University College of Engineering. "Low-cost, ultra-fast DNA sequencing brings diagnostic use closer." ScienceDaily. (accessed December 1, 2015).

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