Identification and mapping of single nucleotide polymorphisms in the human genome
First Claim
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1. A SNP probe consisting of an oligonudeotide that is complementary to a SNP nucleic acid selected from the SNP nucleic acids shown in SEQ ID NOS 64,696-149,311.
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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.
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1 Claim
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1. A SNP probe consisting of an oligonudeotide that is complementary to a SNP nucleic acid selected from the SNP nucleic acids shown in SEQ ID NOS 64,696-149,311.
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Current AssigneeThe SNP Consortium
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Original AssigneeThe SNP Consortium
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InventorsWang, David G.
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Application NumberUS10/027,632Publication NumberTime in Patent OfficeDaysField of SearchUS Class Current536/24.3CPC Class CodesC12Q 1/6883 for diseases caused by alte...C12Q 2600/156 Polymorphic or mutational m...
