SBIR/STTR Research Award

SBIR Phase II: Hybridization and SNP Detection Using Unlabeled Target DNA

Award identifier 5575db2e606a9ea6a9bb17b9dfbc6a22916bfbee8672803c3df43a818711416fAwarding agency National Science Foundation

Award amount

$472,326

Program and phase

SBIR · Phase II

Award year

2009

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Award details

Awarding agency
National Science Foundation
Branch
Not reported
Recipient company
Parallel Synthesis Technologies, Inc
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
NSF 07-551
Topic code
BT

Research abstract

This award is funded under the American Recovery and Reinvestment Act of 2009 Public Law 111-5). This SBIR Phase II project will provide technology to perform remote nucleic acid testing (NAT) in any location. The combination of (a) our Probe-Target-Reporter (PTR) assay which allows the detection of unlabeled Target DNA, (b) our Parallume optical encoding technology which provides the ability to multiplex a large number of samples in each assay and (c) an inexpensive, battery-powered imaging system, based on a $500 commercial CMOS that is completely portable, will be used to build an autonomous NAT platform. This system will be used to detect and defend against the imminent invasion of California's citrus crop by the Liberibacter pathogen and its insect vector/host which causes the 100% fatal and incurable Citrus Greening disease of citrus. Collaborator Isca Technologies will provide a ""Front End"" instrument which can selectively identify an insect by measuring its wing beat frequency as it flies through a laser curtain. This selective insect trap will provide a filtered homogenate of primarily the desired insect vector and pathogen which will be analyzed with our PTR in the field. The data will be relayed to a central database which can provide a real time assessment of the location and bacterial load of the insect vector. The Nucleic Acid Testing (NAT) technology under development as part of this project represents a substantial advance in the ability to perform assays outside of the traditional laboratory or clinical setting. This technology can be used to detect Target DNA sequences without the need to chemically label the sample thereby allowing the NAT analysis to be performed in any location. This NAT technology can be combined with our Parallume optical encoding technology which allows many sample to be measured simultaneously. The ability to analyze many DNA simultaneously without access to a laboratory on a completely portable system will allow NAT to be performed in Low Resource Settings or for Agricultural applications around the world.

Technology keywords

Not reported

Agency intelligence

National Science Foundation

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