Modeling genetic imprinting effects of DNA sequences with multilocus polymorphism data

Single nucleotide polymorphisms (SNPs) represent the most widespread type of DNA sequence variation in the human genome and they have recently emerged as valuable genetic markers for revealing the genetic architecture of complex traits in terms of nucleotide combination and sequence. Here, we extend...

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Hlavní autoři: Wen, Sheron, Wang, Chenguang, Berg, Arthur, Li, Yao, Chang, Myron M, Fillingim, Roger B, Wallace, Margaret R, Staud, Roland, Kaplan, Lee, Wu, Rongling
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2009
Témata:
Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2739217/
https://ncbi.nlm.nih.gov/pubmed/19671182
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1748-7188-4-11
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