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Methods for Genotyping Single Nucleotide Polymorphisms
Annual Review of Genomics and Human Genetics, 2001One of the fruits of the Human Genome Project is the discovery of millions of DNA sequence variants in the human genome. The majority of these variants are single nucleotide polymorphisms (SNPs). A dense set of SNP markers opens up the possibility of studying the genetic basis of complex diseases by population approaches.
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‘Other’ applications of single nucleotide polymorphisms
Trends in Biotechnology, 2007Single nucleotide polymorphisms (SNPs) are the most frequent form of sequence variation in the human genome, occurring on average every 300 base pairs. Owing to their high density, SNPs are considered useful for identifying the genes associated with complex diseases. The focus of this Opinion article is the recent applications of SNPs that fall outside
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Genetic susceptibility and single-nucleotide polymorphisms
Seminars in Fetal and Neonatal Medicine, 2005The completion of the Human Genome Project has provided insight into human genetic variation, most commonly represented by single-nucleotide polymorphisms. There is presently a great deal of interest in linking genetic and phenotypic variation in the form of severity of, and susceptibility to, common multifactorial diseases.
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Linking single nucleotide polymorphisms.
Pharmacogenetics, 2002Nöthen, Markus, Cichon, Sven
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The single nucleotide polymorphism story
Pharmacogenetics, 2003Sandrine Barbaux, Fran ois Cambien
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, 2018