Minimal haplotype tagging

The high frequency of single-nucleotide polymorphisms (SNPs) in the human genome presents an unparalleled opportunity to track down the genetic basis of common diseases. At the same time, the sheer number of SNPs also makes unfeasible genomewide disease association studies. The haplotypic nature of...

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Dades bibliogràfiques

Publicat a:	Proc Natl Acad Sci U S A
Autors principals:	Sebastiani, Paola, Lazarus, Ross, Weiss, Scott T., Kunkel, Louis M., Kohane, Isaac S., Ramoni, Marco F.
Format:	Artigo
Idioma:	Inglês
Publicat:	National Academy of Sciences 2003
Matèries:	Biological Sciences
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC187880/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12900503/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.1633613100
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