Mapping Nucleotide Sequences that Encode Complex Binary Disease Traits with HapMap

Detecting the patterns of DNA sequence variants across the human genome is a crucial step for unraveling the genetic basis of complex human diseases. The human HapMap constructed by single nucleotide polymorphisms (SNPs) provides efficient sequence variation information that can speed up the discove...

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Detalles Bibliográficos
Autores principales: Cui, Yuehua, Fu, Wenjiang, Sun, Kelian, Romero, Roberto, Wu, Rongling
Formato: Texto
Lenguaje:English
Publicado: Bentham Science Publishers Ltd. 2007
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2652402/
https://www.ncbi.nlm.nih.gov/pubmed/19384427
http://dx.doi.org/10.2174/138920207782446188

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2652402/
https://www.ncbi.nlm.nih.gov/pubmed/19384427
http://dx.doi.org/10.2174/138920207782446188

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