Method and system for analyzing biological response signal data

Data processing: measuring – calibrating – or testing – Measurement system in a specific environment – Biological or biochemical

Reexamination Certificate

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C702S020000, C702S021000, C435S006120

Reexamination Certificate

active

06453241

ABSTRACT:

1. FIELD OF THE INVENTION
The present invention relates to the field of computer-assisted analysis of biological information. In particular, the present invention relates to a method and system for management of a database containing biological response signal data and for presentation of useful analytical displays of information therefrom.
2. BACKGROUND OF THE INVENTION
The analysis of complex systems such as biological organisms is aided by the use of relational database systems for storing and retrieving large amounts of biological data. The advent of high-speed wide area networks and the Internet, together with the client/server based model of relational database management systems, is particularly well-suited for allowing researchers to access and meaningfully analyze large amounts of biological data given the appropriate hardware and software computing tools.
Computerized analysis tools are particularly useful in experimental environments involving biological response signals. By way of nonlimiting example, biological response signal data can be obtained and/or gathered using biological response signal matrices, that is, physical matrices of biological material that transmit machine-readable signals corresponding to biological content or activity at each site in the matrix. In these systems, responses to biological or environmental stimuli may be measured and analyzed in a large-scale fashion through computer-based scanning of the machine-readable signals, e.g. photons or electrical signals, into numerical matrices, and through the storage of the numerical data into relational databases.
As a further nonlimiting example, biological response signal data can be obtained and/or gathered using serial analysis of gene expression (SAGE) or other technologies for measuring gene/protein expression levels that may not use a matrix or microarray but otherwise produce measurable signals. Generally speaking, biological response signals may be measured after a perturbation of a biological sample including, for example, the exposure of a biological sample to a drug candidate, the introduction of an exogenous gene into a biological sample, the deletion of a gene from the biological sample, or changes in the culture conditions of the biological sample.
A useful outcome of the scientific experimentation being performed involves the understanding of the relationships between genes and perturbations, understanding that promotes other useful outcomes such as the invention of new drugs or other therapies. Often, relationships between perturbation and gene expression levels sheds light on known or unknown biological pathways. There is an ongoing need in the art to generate better and more useful ways for computers to assist in analyzing the large volume of biological response data that can exist for even the most simple biological organisms.
3. SUMMARY OF THE INVENTION
A system, method, and computer program product are provided for improved computer-aided analysis of biological data derived from machine readable outputs of experiments performed on a plurality of biological samples. Responsive to search and execution commands from the user, a plurality of biological viewer windows are spawned on a user computer display. The user may then select a source dataset from one of the biological viewers and execute a project selection command, wherein the source dataset is then projected onto the other biological viewers. The projections are characterized by a highlighted display of biological data points in the destination biological viewers corresponding to items in the source dataset. The selected data is highlighted in the destination biological viewers using contrast or color differentiation from other destination window data.
In another preferred embodiment, the user may spawn a hierarchical cluster tree biological viewer that displays genes or experiments grouped based on similarity of behavior, wherein the hierarchical cluster tree is displayed in a hyperbolic display fashion. In one form, the hierarchical cluster tree may be, for example, a gene coregulation tree. When displayed in a hyperbolic display fashion, convenient viewing of the hierarchical cluster tree is enabled, whereby the user may move around the tree and zoom in and out of various areas of the tree without losing perspective of their current location relative to the “root” of the tree.
In another preferred embodiment, biological menu and submenu items that are displayed to the user during searches, projections, and the like are not stored in the user computer, but rather are stored in a central biological response database. Biological menus and submenus are generated at startup based on queries to the central biological response database, allowing for increased flexibility, changeability, and customization of the biological menus and submenus.
In another preferred embodiment, correlation data between expression array experiments is precomputed when the experiments are added to the central biological response database. This eliminates the need for real time computation of correlation coefficients or other similarity scores by the user computer, resulting in considerable time savings when the user requests correlation data among selected sets of experiments.


REFERENCES:
patent: 5181162 (1993-01-01), Smith et al.
patent: 5338659 (1994-08-01), Kauvar et al.
patent: 5510270 (1996-04-01), Fodor et al.
patent: 5556752 (1996-09-01), Lockhart et al.
patent: 5569588 (1996-10-01), Ashby et al.
patent: 5578832 (1996-11-01), Trulson et al.
patent: 5586033 (1996-12-01), Hall
patent: 5590250 (1996-12-01), Lamping et al.
patent: 5619632 (1997-04-01), Lamping et al.
patent: 5630125 (1997-05-01), Zellweger
patent: 5777888 (1998-07-01), Rine et al.
patent: 5966712 (1999-10-01), Sabatini et al.
patent: 5970500 (1999-10-01), Sabatini et al.
patent: 6165709 (2000-12-01), Friend et al.
patent: 6185561 (2001-02-01), Balaban et al.
patent: 6203987 (2001-03-01), Friend et al.
patent: 6245517 (2001-06-01), Chen et al.
patent: WO 97/27317 (1996-01-01), None
patent: WO 97/10365 (1996-09-01), None
Eisen, et al., 1998, “Cluster Analysis and Display of Genome-Wide Expression Patterns,”Proc. Natl. Acad. Sci., USA, 95: 14863-14868.
Duda et al., 2001,Pattern Classification, Second Edition, A Wiley-Interscience Publication, Chapter 10: 550-555.
Sokal et al., 1958, “A Statistical Method for Evaluating Systematic Relationships,”The University of Kansas Science Bulletin, vol. 38: 1409-1438.
Weinstein et al. (Science 275, 343-349, 1997).*
Zhao et al. 1995, “High-density cDNA filter analysis: a novel approach for large-scale, quantitative analysis of gene expression,”Gene 156: 207-213.
Blanchard et al., 1996, “Sequence to array: Probing the genome's secrets,”Nature Biotechnology 14:1649.
Blanchard et al., 1996, “High-Density Oligonucleotide Arrays,”Biosensors&Bioelectronics 11:687-90.
Chee et al., 1996, “Accessing Genetic Information with High-Density DNA Arrays,”Science 274:610-614.
Chait, 1996, “Trawling for proteins in the post-genome era,”Nat. Biotech. 14:1544.
DeRisi et al., 1996, “Use of a cDNA microarray to analyze gene expression patterns in human cancer,” Nature Genetics 14:457-460.
DeRisi et al., 1997, “Exploring the metabolic and genetic control of gene expression on a genomic scale,”Science 278:680-686.
Lamping and Rao, 1994, “Laying out and Visualizing Large Trees Using a Hyperbolic Space,”UIST '94Nov. 2-4, 1994. Jul. 13, 1999Marina del Rey, California. pp. 13 and 14.
Lockhart et al., 1996, “Expression monitoring by hybridization to high-density oligonucleotide arrays,”Nature Biotechnology 14:1675-1680.
Marton et al., 1998, “Drug target validation and identification of secondary drug target effects using DNA microarrays,”Nat. Med. 4(11):1293-1301.
McCormack et al., 1997, “Direct analysis and identification of proteins in mixtures by LC/MS/MS and database searching at low-femtomole level”,Anal. Chem. 69:767-776.
Schena et al., 1995, “Quantitative monitoring of gene expression patterns with a complementary DNA micro-array,”Science 270: 467-470.

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