IP Library Granted Patent US 7,904,250
Granted Patent B2
US 7,904,250 · App. 11/043,294 · Granted Mar 8, 2011

Computer software to assist in identifying SNPS with microarrays

Assignee: Roche Nimblegen, Inc.
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Quick Facts
Patent No.
US 7,904,250
App. No.
11/043,294
Granted
Mar 8, 2011
Kind
B2
Abstract

The present invention is a method to assist in the identification of single nucleotide polymorphisms (SNP) from microarray hybridization data. Data from hybridization protocols run on microarrays often have variations in the data resulting from variations in hybridization conditions and efficiencies and variations in optical intensities. An algorithm is described to screen the results to identify those data points most likely to be real SNPs as opposed to variations in the hybridization or sensing data.

Claims (10)

1. A method for identifying in a sample single nucleotide polymorphisms relative to a reference nucleotide at a position in a reference sequence, the method comprising the steps of:

hybridizing the sample to a microarray of oligonucleotide probes, the microarray comprising, for each reference nucleotide, a first probe complementary to the reference sequence and second, third and fourth probes complementary to the reference sequence except for a non-matching nucleotide at the position, the four probes defining a position group at a physical space on the microarray, the nucleotide at the position on each probe in the position group being unique and being selected from the group consisting of A, G, C and T;

determining the relative hybridization intensity of each probe in each position group;

classifying each position group as a conformer if the highest intensity probe conforms to the reference sequence at the position, as a nonconformer if the highest intensity probe does not conform to the reference sequence at the position;

mapping the conformers and nonconformers to their physical space on the microarray;

identifying as possible SNPs only those nonconformers physically located adjacent on the microarray to conformers; and

outputting the identification of possible SNPs to a user.

2. A method as claimed in claim 1 wherein said mapping comprises using a machine learning algorithm to map the conformers and nonconformers.

3. A method as claimed in claim 2 wherein the machine learning algorithm is a nearest neighbor algorithm.

4. A method as claimed in claim 1 wherein the position is at a central position of each probe in the position group.

Assignments (2)
CHANGE OF NAME Recorded Jan 24, 2011
From: NIMBLEGEN SYSTEMS, INC.
To: ROCHE NIMBLEGEN, INC.
Reel/Frame 025685/0436 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 6, 2007
From: MOLLA, MICHAEL; RICHMOND, TODD; SMITH, STEVEN; ALBERT, THOMAS
To: NIMBLEGEN SYSTEMS, INC.
Reel/Frame 018965/0775 →
Continuity (2)
Provisional Application 60539220 · Jan 26, 2004
Related Publication 20060014164A1 · Jan 19, 2006