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:
Apr. 22, 2008

Filed:

Jul. 05, 2005
Applicants:

Guoying Liu, Emeryville, CA (US);

Simon Cawley, Oakland, CA (US);

Hajime Matsuzaki, Palo Alto, CA (US);

Earl A. Hubbell, Palo Alto, CA (US);

Geoffrey Yang, San Jose, CA (US);

Teresa A. Webster, Santa Clara, CA (US);

Rui Mei, Santa Clara, CA (US);

Xiaojun Di, Cupertino, CA (US);

Richard Chiles, Castro Valley, CA (US);

Inventors:

Guoying Liu, Emeryville, CA (US);

Simon Cawley, Oakland, CA (US);

Hajime Matsuzaki, Palo Alto, CA (US);

Earl A. Hubbell, Palo Alto, CA (US);

Geoffrey Yang, San Jose, CA (US);

Teresa A. Webster, Santa Clara, CA (US);

Rui Mei, Santa Clara, CA (US);

Xiaojun Di, Cupertino, CA (US);

Richard Chiles, Castro Valley, CA (US);

Assignee:

Affymetrix, Inc., Santa Clara, CA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C12Q 1/68 (2006.01); C07H 21/04 (2006.01); C12M 3/00 (2006.01); C12M 1/34 (2006.01);
U.S. Cl.
CPC ...
Abstract

Methods, kits and arrays of nucleic acid probes for genotyping large numbers of human SNPs in parallel are provided. A set of more than 100,000 human SNPs, known to be biallelic in at least two populations is provided. Allele specific perfect match probes and genotyping probe sets are provided for each allele of each biallelic SNP in a set of human SNPs that is useful for genetic analysis within and across populations. Probe sets that include perfect match and mismatch probes are provided. The probe sets are suitable for inclusion in an array. The invention provides the SNP and surrounding sequence and provides the sequences in such a way as to make them available for a variety of analyses including genotyping. As such, the invention relates to diverse fields impacted by the nature of genetics, including biology, medicine, and medical diagnostics.


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