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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...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2739217/ https://www.ncbi.nlm.nih.gov/pubmed/19671182 http://dx.doi.org/10.1186/1748-7188-4-11 |