March 6, 2017 Credit: University of New Mexico <\/p>\n
A young company developing technology created at the University of New Mexico (UNM) is on a mission to disrupt the landscape of DNA sequencing. <\/p>\n
Armonica Technologies, LLC, is developing a DNA sequencing platform that will sequence a complete human genome in minutes. The company's goal is to make the technology the gold standard for DNA sequencing for precision medicine research applications. Armonica has optioned a portfolio of patented and patent pending technologies from STC.UNM. The technology is called \"optical nanopore sequencing\" and uses nanochannels to deliver single DNA molecules through nanopores. Nanopores are very small holes with an internal diameter of 1 nanometer (one billionth of a meter). The nanopores slow down DNA translocation enough to produce massively parallel, single-base resolution using optical techniques. <\/p>\n
Here's how nanopore sequencing works: when a nanopore is immersed in conducting fluid, voltage can be applied to produce an electric current. The current is sensitive to the size and shape of the nanopore so that if a DNA strand passes through or near the nanopore, the amount of current changes. The change in the current as the DNA molecule passes through the nanopore represents a reading of the DNA sequence. <\/p>\n
\"There is an unmet need in the fast-growing DNA sequencing market,\" said Armonica President & CEO Scott Goldman. \"Today's standard genome sequencing approach requires extensive library preparation and creates a massive computational and bioinformatics problem related to reassembling the data set. Armonica will resolve these problems by introducing a sequencing instrument that will not require library preparation and will generate reads of up to 50,000 bases, combined with a parallelism of 1 million. This approach will net 50 billion basesmore than sufficient to sequence the entire human genome in minutes.\" <\/p>\n
The innovative nanopore technology was developed by Distinguished Professor Emeritus Steve Brueck, Research Assistant Professor Yuliya Kuznetsova, and Postdoctoral Fellow Alexander Neumann from UNM's Center for High Technology Materials (CHTM) and Professor Jeremy Edwards from UNM's Department of Chemistry & Chemical Biology, in collaboration with Redondo Optics CEO Edgar Mendoza. <\/p>\n
\"Nanopore sequencing analyzes long DNA strings, with long reads that provide more accurate identification of genome variations,\" said Brueck. \"It is an approach, therefore, that leads to a more thorough, faster, and accurate genomic analysis, allowing researchers to substantially improve the ability to make new discoveries. One of the challenges of nanopore sequencing is to improve the resolution to be able to detect single nucleotides (bases).\" <\/p>\n
\"We believe our nanochannel technology will disrupt the industry because it produces very long reads for higher accuracy, very high parallelism using optical techniques, and high throughput rates for greater processing speed. It will be an affordable tool for researchers,\" said STC CEO Lisa Kuuttila. \"This technology portfolio represents a leap in genomic sequencing technology that could be a huge benefit for the DNA sequencing industry, which is experiencing explosive growth. The company's research and development are currently being done at UNM's CHTM, a research center with a global reputation for inventing disruptive nanoscale technologies and providing outstanding scientific expertise and technical support. We are very excited about the technology's potential and believe in the company's vision.\" <\/p>\n
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Continue reading here: March 6, 2017 Credit: University of New Mexico A young company developing technology created at the University of New Mexico (UNM) is on a mission to disrupt the landscape of DNA sequencing. Armonica Technologies, LLC, is developing a DNA sequencing platform that will sequence a complete human genome in minutes. The company's goal is to make the technology the gold standard for DNA sequencing for precision medicine research applications. Continue reading
\nPushing the boundaries of DNA sequencing - Phys.Org<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"