The present invention is directed to spectroscopic analysis and more particularly to a technique to improve the accuracy of spectroscopic analysis.
Spectroscopy is a well known technique to analyze the spectral properties associated with a source, such as a substance or object/scene being imaged, in order to identify compounds in the substance or particular objects in the scene. For example, spectroscopic techniques are used in Raman scattering techniques whereby a sample is illuminated with light and the spectrum of the scattered energy from the substance is analyzed to identify a specific substance as being present in the sample. High correlation between spectra of different substances, spectral clutter, and noise limit the sensitivity (i.e., decrease the probability of correct detection and identification) and specificity (i.e., increase false alarm rate) for many currently available spectroscopic techniques.
What is needed is a spectroscopic detection technique and system that is more accurate than techniques heretofore known.
Briefly, the present invention is directed a spectroscopic featured-based detection or identification system and method. The present invention uses the primary or main spectroscopic features of a source, such as those as arising from chemical functional groups, to describe and distinguish the source. These primary spectroscopic features make up a portion (i.e., are a subset) of the entire spectroscopic data for a particular source but can nevertheless be used as the basis of separating spectra from multiple sources. Thus, when analyzing spectroscopic data obtained from a sample for one or more sources, the analysis first focuses on the primary spectroscopic features for a source rather than the entire spectra for a source. This techniques reduces the correlation between sources of interest and other sources and makes it easier for an identifier to achieve optimum performance (i.e., reduced false alarms and maximum detections).
Thus, according to the present invention a method is provided for analyzing spectroscopic data to separate spectral data for at least one source from the spectroscopic data. The primary spectral features of the spectroscopic data for one or more sources of interest are identified and data is stored for the primary spectral features of the at least one source. Then, spectroscopic data is obtained from a sample and is first analyzed with the stored data for the primary spectral features to eliminate from consideration a source whose primary spectral features are not present in the spectroscopic data for the sample. The spectroscopic data for the sample is further analyzed using knowledge of one or more sources that are eliminated by the first analysis, in order to identify one or more sources present in the sample. The source may be a substance of interest, such as a chemical or biological agent, or may be a particular object of interest in an imaged scene.
The present invention is directed to improving the accuracy of spectroscopic analysis techniques, such as used in techniques for spectroscopic-based substance detection or spectroscopic-based imagery by introducing an analysis step that eliminates sources whose primary or main spectral features are not present in the sample spectroscopic data. Thus, the term source is used herein to include, without limitation a substance that has a spectral signature, as well as an object that has a spectral signature when a spectral imagery is employed. Examples of substances are chemical, biological or other compounds, in solid, liquid or gas form. For example, a substance of interest may be an agent of chemical and/or biological makeup that is harmful to humans, and thus whose presence is desired to be detected. Examples of objects of interest are military vehicles hidden under trees detected through sub-pixel processing of their spectral data to identify the presence of material the vehicles are made of.
Referring first to
Turning to
Thus, in the spectral feature determination process 100, the spectroscopic data for a source of interest is captured at 110 (e.g., from stored spectroscopic data for that source), where the spectroscopic data may have been obtained in a laboratory or field environment at some prior point in time. At 120, the spectroscopic data for the source is analyzed to determine its main or primary spectral features. This may involve examining the shapes, location of spikes, height of spikes, etc., as compared with the spectral data for other sources. Features are determined through means such as correlation analysis (in order to determine the most prominent features for a given agent) or functional group analysis which consists of inspecting the primary chemical bonds between atoms forming a molecule. At 130, data is stored to represent the primary spectral features determined at 120, such as in a database shown at reference numeral 200 shown in
Turning to
At 330, a second analysis is performed of the spectroscopic data for the remaining possible features, thereby more closely analyzing the spectroscopic data against the reduced library spectra.
The spectroscopic techniques described herein may be used in any source-separation process for any type of data, including multispectral and hyperspectral imagery for military and non-military applications.
The system and methods described herein may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The foregoing embodiments are therefore to be considered in all respects illustrative and not meant to be limiting.
Number | Name | Date | Kind |
---|---|---|---|
6788407 | Higdon et al. | Sep 2004 | B1 |
6834122 | Yang et al. | Dec 2004 | B2 |
6847446 | Shilling | Jan 2005 | B2 |
6922645 | Haaland et al. | Jul 2005 | B2 |
6949734 | Neff et al. | Sep 2005 | B2 |
7009170 | Dobbs et al. | Mar 2006 | B2 |
7099003 | Saptari et al. | Aug 2006 | B2 |
7127372 | Boysworth | Oct 2006 | B2 |
7333190 | Pendell-Jones et al. | Feb 2008 | B1 |
7359040 | Pendell-Jones et al. | Apr 2008 | B1 |
20010052978 | Lewis et al. | Dec 2001 | A1 |
20020031843 | Harmon | Mar 2002 | A1 |