Granted Patent
H1
US 2,191 · App. 09/925,065 · Granted Jun 5, 2007
Identification and mapping of single nucleotide polymorphisms in the human genome
Assignee:
SNP Consortium
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Abstract
The invention relates to the role of genes in human diseases. More particularly, the invention relates to compositions and methods for identifying genes that are involved in human disease conditions. The invention provides identification and mapping of a very large number of SNPs throughout the entire human genome. This contribution allows scientists to isolate and identify genes that are relevant to the prevention, causation, or treatment of human disease conditions.
Claims (1)
1. A SNP probe consisting of an oligonucleotide that is complementary to a SNP nucleic acid selected from the SNP nucleic acids shown in SEQ ID NOs: 1-12,108.
Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST
Recorded Sep 24, 2001
From: WANG, DAVID G.
To: SNP CONSORTIUM, THE
Reel/Frame 012198/0390 →
Continuity (7)
Provisional Application
6024309600
· Oct 24, 2000
Provisional Application
6025214700
· Nov 20, 2000
Provisional Application
6025009200
· Nov 30, 2000
Provisional Application
6026176600
· Jan 16, 2001
Provisional Application
6028984600
· May 9, 2001
Related Publication
20050228172A9
· Sep 16, 2004