Skip to main content
Premium Trial:

Request an Annual Quote

Stratos Genomics Awarded Access to Microfabrication Lab to Develop Nanopore Sequencing Tech


This article was originally published on January 8, 2010.

Stratos Genomics, a Seattle-based biotech startup, has won access to a microfabrication laboratory run by the Washington Technology Center, an economic development organization, "to further its DNA sequencing product development," WTC said last week.

According to WTC, Stratos Genomics is developing a new DNA sequencing method "that will dramatically reduce the time and costs of high-throughput DNA sequencing."

The award will allow Stratos Genomics to access WTC's Seattle-based microfabrication facility for three months for a proposal entitled "Nanopore Noise Reduction Project." According to WTC, the project aims to meet a technical goal that is part of a proof of concept for Stratos' technology, which "creates, encodes, and measures surrogate molecules derived from DNA targets to produce DNA sequence information."

"Successful demonstration of the technology will open the door for company growth to address the next commercialization steps," according to WTC.

WTC made the award under a new technology stimulus program that grants small businesses in Washington access to its 15,000-square-foot microfabrication laboratory. The lab includes facilities and specialized equipment for microelectromechanical systems, or MEMS, research and product or process development.

According to its website, WTC helps companies develop and commercialize new products and technologies by channeling state, federal, and private resources.

Stratos Genomics, founded in 2008, is part of Stratos, which designs and develops products for a variety of companies, including Microsoft, Abbott Laboratories, Nike, and Spacelabs Medical.

The Scan

Genetic Tests Lead to Potential Prognostic Variants in Dutch Children With Dilated Cardiomyopathy

Researchers in Circulation: Genomic and Precision Medicine found that the presence of pathogenic or likely pathogenic variants was linked to increased risk of death and poorer outcomes in children with pediatric dilated cardiomyopathy.

Fragile X Syndrome Mutations Found With Comprehensive Testing Method

Researchers in Clinical Chemistry found fragile X syndrome expansions and other FMR1 mutations with ties to the intellectual disability condition using a long-range PCR and long-read sequencing approach.

Team Presents Strategy for Speedy Species Detection in Metagenomic Sequence Data

A computational approach presented in PLOS Computational Biology produced fewer false-positive species identifications in simulated and authentic metagenomic sequences.

Genetic Risk Factors for Hypertension Can Help Identify Those at Risk for Cardiovascular Disease

Genetically predicted high blood pressure risk is also associated with increased cardiovascular disease risk, a new JAMA Cardiology study says.