SBIR-STTR Award

Novel Sequencing by Synthesis Platform to Greatly Reduce the Cost of Nucleic Acid Sequencing
Award last edited on: 4/30/2020

Sponsored Program
SBIR
Awarding Agency
NIH : NHGRI
Total Award Amount
$2,224,579
Award Phase
2
Solicitation Topic Code
-----

Principal Investigator
Mark R Pratt

Company Information

Ultima Genomics Inc

7979 Gateway Boulevard
Newark, CA 94560
   (510) 432-8786
   N/A
   www.ultimagen.com
Location: Single
Congr. District: 17
County: Alameda

Phase I

Contract Number: 1R44HG010558-01
Start Date: 5/22/2019    Completed: 9/17/2019
Phase I year
2019
Phase I Amount
$299,441
Ultima Genomics, Inc. proposes to develop a novel high-throughput sequencing technology platform that will reduce cost ($/Gbase) substantially compared with state-of-the-art commercial technologies. The new technol- ogy to be developed in the SBIR project will particularly benefit DNA sequencing applications that are cost constrained, such as sequencing large populations, generating methylation and transcriptome profiles for millions of single cells, and enabling liquid biopsy applications. Target customers include genome centers, CROs, research labs, and clinical labs. The company is pioneering a series of inter-related innovations that mutually reinforce one another in a virtu- ous circle to achieve much lower cost. In Phase 1 of the FastTrack project, the 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 samples. In Phase 2, the company will further develop the core plat- form technology; build a beta instrument that achieves highly competitive specifications for accuracy, read length, throughput, time to answer, and cost; and validate performance rigorously using multiple reference samples. By dramatically reducing sequencing cost, Ultima Genomics' technology will directly impact a wide range of scientific capabilities with direct relevance for public health, including characterization of tumors, detection of early stage cancers through blood test, and personalized/precision medicine.

Public Health Relevance Statement:
PROJECT NARRATIVE The proposed project will develop new instrumentation and methodologies that will substantially reduce the cost to perform genome-scale sequencing. This cost reduction will accelerate a diverse range of biomedical re- search efforts that aim to understand the genetic factors that play a role in human disease and to develop new diagnostics and therapeutics. It will also make both existing and new sequencing-based diagnostic tests more affordable, so they can become routine constituents of standards of care. !

Project Terms:
Algorithmic Analysis; Bacteriophage lambda; base; Blood Tests; Caring; Cells; Chemistry; Cicatrix; Cleaved cell; Clinical; cost; Cost Savings; Detection; Development; Diagnostic tests; DNA amplification; DNA sequencing; Dyes; Early Diagnosis; Engineering; Environment; Escherichia coli; evaporation; Fluorescence; Fluorescent Dyes; Flushing; Formulation; Funding; Genetic; Genome; genome-wide; Genomics; High-Throughput Nucleotide Sequencing; Hour; Human; human disease; Human Genome; human reference genome; Image; Image Analysis; Immersion Investigative Technique; improved; innovation; instrument; instrumentation; Label; Length; lens; Libraries; liquid biopsy; Liquid substance; Malignant Neoplasms; Methodology; Methylation; new technology; novel; novel diagnostics; novel therapeutics; Nucleic acid sequencing; Nucleotides; Performance; Phase; Play; Polymerase; Population; precision medicine; Preparation; Privatization; Protocols documentation; prototype; public health relevance; Reagent; Research; Resolution; Role; Rotation; Sampling; Scanning; sequencing platform; Series; Shotgun Sequencing; Shotguns; Small Business Innovation Research Grant; Speed; Surface; System; Techniques; Technology; Thick; Thinness; Time; transcriptome; transcriptome sequencing; tumor; Work

Phase II

Contract Number: 4R44HG010558-02
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
2019
Phase II Amount
$1,925,138
Ultima Genomics, Inc. proposes to develop a novel high-throughput sequencing technology platform that will reduce cost ($/Gbase) substantially compared with state-of-the-art commercial technologies. The new technology to be developed in the SBIR project will particularly benefit DNA sequencing applications that are cost constrained, such as sequencing large populations, generating methylation and transcriptome profiles for millions of single cells, and enabling liquid biopsy applications. Target customers include genome centers, CROs, research labs, and clinical labs. The company is pioneering a series of inter-related innovations that mutually reinforce one another in a virtuous circle to achieve much lower cost. In Phase 1 of the FastTrack project, the 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 samples. In Phase 2, the company will further develop the core platform technology; build a beta instrument that achieves highly competitive specifications for accuracy, read length, throughput, time to answer, and cost; and validate performance rigorously using multiple reference samples. By dramatically reducing sequencing cost, Ultima Genomics' technology will directly impact a wide range of scientific capabilities with direct relevance for public health, including characterization of tumors, detection of early stage cancers through blood test, and personalized/precision medicine.

Public Health Relevance Statement:
PROJECT NARRATIVE The proposed project will develop new instrumentation and methodologies that will substantially reduce the cost to perform genome-scale sequencing. This 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 therapeutics. It will also make both existing and new sequencing-based diagnostic tests more affordable, so they can become routine constituents of standards of care.

Project Terms:
Algorithmic Analysis; Bacteriophage lambda; base; Biomedical Research; Blood Tests; Caring; Cells; Chemistry; Cicatrix; Cleaved cell; Clinical; cost; Cost Savings; Detection; Development; Diagnostic tests; DNA amplification; DNA sequencing; Dyes; Early Diagnosis; Engineering; Environment; Escherichia coli; evaporation; Fluorescence; Fluorescent Dyes; Flushing; Formulation; Funding; Genetic; Genome; genome-wide; Genomics; High-Throughput Nucleotide Sequencing; Hour; Human; human disease; Human Genome; human reference genome; Image; Image Analysis; Immersion Investigative Technique; improved; innovation; instrument; instrumentation; Label; Length; lens; Libraries; liquid biopsy; Liquid substance; Malignant Neoplasms; Methodology; Methylation; new technology; novel; novel diagnostics; novel therapeutics; Nucleic acid sequencing; Nucleotides; Performance; Phase; Play; Polymerase; Population; precision medicine; Preparation; Privatization; Protocols documentation; prototype; public health relevance; Reagent; Research; Resolution; Role; Rotation; Sampling; Scanning; sequencing platform; Series; Shotgun Sequencing; Shotguns; Small Business Innovation Research Grant; Speed; Surface; System; Techniques; Technology; Thick; Thinness; Time; transcriptome; transcriptome sequencing; tumor; Work