SBIR/STTR Research Award

Novel sequencing by synthesis platform to greatly reduce the cost of nucleic acid sequencing

Award identifier ee2d29661f18806d3146c20c097a632868d3af0880d3b643ed357f863c00f04cAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$299,441

Program and phase

SBIR · Phase I

Award year

2019

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Ultima Genomics, Inc.
Proposal award date
2019-05-22
Contract end date
2019-09-17
UEI
DXEVRGJ7MW28
Solicitation number
HG18-003
Topic code
172

Research abstract

PROJECT SUMMARY Ultima GenomicsIncproposes to develop a novel high throughput sequencing technology platform that will reduce cost$ Gbasesubstantially compared with state of the art commercial technologiesThe new technology to be developed in the SBIR project will particularly benefit DNA sequencing applications that are cost constrainedsuch as sequencing large populationsgenerating methylation and transcriptome profiles for millions of single cellsand enabling liquid biopsy applicationsTarget customers include genome centersCROsresearch labsand clinical labsThe company is pioneering a series of inter related innovations that mutually reinforce one another in a virtuous circle to achieve much lower costIn Phaseof the FastTrack projectthe company will integrate these separate innovations into an alpha prototype and prove the feasibility of the platform by performing shotgun sequencing of human genome reference samplesIn Phasethe company will further develop the core platform technologybuild a beta instrument that achieves highly competitive specifications for accuracyread lengththroughputtime to answerand costand validate performance rigorously using multiple reference samplesBy dramatically reducing sequencing costUltima Genomicsandapostechnology will directly impact a wide range of scientific capabilities with direct relevance for public healthincluding characterization of tumorsdetection of early stage cancers through blood testand personalized precision medicine PROJECT NARRATIVE The proposed project will develop new instrumentation and methodologies that will substantially reduce the cost to perform genome scale sequencingThis cost reduction will accelerate a diverse range of biomedical research efforts that aim to understand the genetic factors that play a role in human disease and to develop new diagnostics and therapeuticsIt will also make both existing and new sequencing based diagnostic tests more affordableso they can become routine constituents of standards of care!

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

3 SBIR/STTR records share this UEI (2019–2020). Reported award amounts total $4,224,443. Reported amounts are not federal obligations.

Phases: Phase II, Phase I, Phase II – Direct to Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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