SBIR-STTR Award

Sample Classification and Biomarker Discovery by Comprehensive Metabolomic Analysis
Award last edited on: 12/28/2023

Sponsored Program
SBIR
Awarding Agency
NSF
Total Award Amount
$1,004,614
Award Phase
2
Solicitation Topic Code
BC
Principal Investigator
Stephen E Reichenbach

Company Information

GC Image LLC (AKA: GC Image ~ GC Imaging)

201 North 8th Street Suite 420
Lincoln, NE 68508
   (402) 310-4503
   info@gcimage.com
   www.gcimage.com
Location: Single
Congr. District: 01
County: Lancaster

Phase I

Contract Number: 1013180
Start Date: 7/1/2010    Completed: 6/30/2011
Phase I year
2010
Phase I Amount
$174,643
This Small Business Innovation Research (SBIR) Phase I project proposes to develop a system for automated classification of biological samples and discovery of biomarkers. The goal is a system to perform comprehensive pattern analysis of state-of-the-art biochemical separations generated by comprehensive two-dimensional gas chromatography (GCxGC) with high-resolution mass spectrometry (HRMS). A critical challenge for elective utilization of GCxGC-HRMS for biochemical classification and biomarker discovery is the diffculty of analyzing and interpreting the massive, complex data for metabolomic and proteomic features. The quantity and complexity of the data, as well as the large dimensionality of the biochemistry in which significant characteristics may be subtle and involve patterns of variations in multiple constituents, necessitate the investigation and development of new bioinformatics. The principal technical objective is an innovative framework for comprehensive feature matching and analysis across many samples. Feature matching is the basis for uniformly labeling structures so that similarities and differences can be documented. Specifically, the framework will incorporate advanced methods for multidimensional peak detection, peak pattern matching across large sample sets, data alignment, GCxGC-HRMS feature computations, and classification with large feature sets. The anticipated result is the technical foundation for a commercial system to classify biological samples and identify significant biomarkers. The broader impact/commercial potential of this project, if successful, will be a better understanding of biochemical processes and discovery of metabolomic and proteomic biomarkers, leading to improved methods for disease diagnoses and treatments. These innovative bioinformatics will contribute to economic competitiveness in the global market for analytical technologies and will foster utilization of advanced GCxGC-HRMS instrumentation. The informatics developed in this project also will be relevant for other classification problems involving multidimensional, multispectral data, including other applications (such as biofuels),other types of chemical analyses (such as multidimensional spectroscopy), and other fields (such as remote-sensing multispectral geospatial imagers). The project will contribute to workforce development, by involving student interns in research experiences through internships and project sponsorships, and to education, by providing software and example data to allow students to more easily explore biochemical complexity

Phase II

Contract Number: 1127264
Start Date: 10/1/2011    Completed: 8/31/2016
Phase II year
2011
(last award dollars: 2015)
Phase II Amount
$829,971

This Small Business Innovation Research Phase II project proposes to develop a system for automated classification of biological samples and discovery of biomarkers. The system will be designed to perform comprehensive pattern analysis of state-of-the-art biochemical separations generated by comprehensive two-dimensional chromatography (GCxGC) with high-resolution mass spectrometry (HRMS). The pairing of GCxGC and HRMS combines highly effective molecular separations with precise elemental analysis. A critical challenge for effective utilization of GCxGC-HRMS for biochemical sample classification and biomarker discovery is the difficulty of analyzing and interpreting the massive, complex data for metabolomic features. The quantity and complexity of the data, as well as the large dimensionality of the metabolome, and the possibility that significant chemical characteristics may be subtle and involve patterns of multiple constituents, necessitate investigation and development of new bioinformatics. The principal technical objective is an innovative framework for comprehensive feature matching and analysis across many samples. Specifically, the framework will incorporate advanced methods for multidimensional peak detection, peak pattern matching across large sample sets, data alignment, comprehensive feature matching, and multi-sample analyses (e.g., classification and biomarker discovery) with large sample sets. The anticipated result is a commercial system for automated multi-sample analysis. The broader impact/commercial potential of this project will be realized through improved informatics for biological classification and biomarker discovery. These tools will enable researchers to better understand biochemical processes and to discover metabolic biomarkers, which could lead to improved methods for disease diagnoses and treatments. These information technologies will foster utilization of advanced GCxGC-HRMS instrumentation, thereby contributing to the impetus for future instrument development. The informatics developed in this project also will be relevant for other classification problems involving multidimensional, multispectral data, including other applications (such as biofuels), other types of chemical analyses (such as multidimensional spectroscopy), and other fields (such as remote-sensing multispectral geospatial imagers). This project will contribute to national competitiveness in the global market for analytical technologies and will contribute to workforce development by involving students in research experiences through internships and student projects. Software developed in the project and an example dataset will be available to educational institutions to allow students to more easily explore biochemical complexity