A SNP (pronounced "snip") is a substitution of one base pair at a given location on the genome. At position 11,294,479 on human chromosome 7, for instance, some people have an A, while others have a G ...

The current catalog makes it clear that our ability to find SNPs already outstrips our capacity to genotype them by at least 1,000-fold. Although many approaches for SNP genotyping have emerged ...

Single nucleotide polymorphisms (SNPs) are major contributors to genetic variation, comprising some 80% of all known polymorphisms, and their density in the human genome is estimated to be on ...

The Genomics Core Laboratory has the capability of performing standard fluorescent and Next-Generation Sequencing (NGS), high and low throughput custom genotyping from 1 SNP to more than 5 million ...