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High-throughput discovery of rare human nucleotide polymorphisms by Ecotilling

Human individuals differ from one another at only ∼0.1% of nucleotide positions, but these single nucleotide differences account for most heritable phenotypic variation. Large-scale efforts to discover and genotype human variation have been limited to common polymorphisms. However, these efforts ove...

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Detalles Bibliográficos
Autores principales: Till, Bradley J., Zerr, Troy, Bowers, Elisabeth, Greene, Elizabeth A., Comai, Luca, Henikoff, Steven
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1540726/
https://www.ncbi.nlm.nih.gov/pubmed/16893952
http://dx.doi.org/10.1093/nar/gkl479