The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Aug. 08, 2006

Filed:

Dec. 27, 2004
Applicants:

Christopher H. Becker, Palo Alto, CA (US);

Curtis A. Hastings, Bethesda, MD (US);

Scott M. Norton, Durham, NC (US);

Sushmita Mimi Roy, Santa Clara, CA (US);

Weixun Wang, Mountain View, CA (US);

Haihong Zhou, Mountain View, CA (US);

Thomas Andrew Shaler, Fremont, CA (US);

Praveen Kumar, Santa Clara, CA (US);

Markus Anderle, Campbell, CA (US);

Hua Lin, Sunnyvale, CA (US);

Inventors:

Christopher H. Becker, Palo Alto, CA (US);

Curtis A. Hastings, Bethesda, MD (US);

Scott M. Norton, Durham, NC (US);

Sushmita Mimi Roy, Santa Clara, CA (US);

Weixun Wang, Mountain View, CA (US);

Haihong Zhou, Mountain View, CA (US);

Thomas Andrew Shaler, Fremont, CA (US);

Praveen Kumar, Santa Clara, CA (US);

Markus Anderle, Campbell, CA (US);

Hua Lin, Sunnyvale, CA (US);

Assignee:
Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
B01D 59/44 (2006.01); H01J 49/00 (2006.01);
U.S. Cl.
CPC ...
Abstract

Relative quantitative information about components of chemical or biological samples can be obtained from mass spectra by normalizing the spectra to yield peak intensity values that accurately reflect concentrations of the responsible species. A normalization factor is computed from peak intensities of those inherent components whose concentration remains constant across a series of samples. Relative concentrations of a component occurring in different samples can be estimated from the normalized peak intensities. Unlike conventional methods, internal standards or additional reagents are not required. The methods are particularly useful for differential phenotyping in proteomics and metabolomics research, in which molecules varying in concentration across samples are identified. These identified species may serve as biological markers for disease or response to therapy.


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