Optimal Haplotype Block-Free Selection of Tagging SNPs for Genome-Wide Association Studies

It is widely hoped that the study of sequence variation in the human genome will provide a means of elucidating the genetic component of complex diseases and variable drug responses. A major stumbling block to the successful design and execution of genome-wide disease association studies using singl...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Halldórsson, Bjarni V., Bafna, Vineet, Lippert, Ross, Schwartz, Russell, De La Vega, Francisco M., Clark, Andrew G., Istrail, Sorin
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Cold Spring Harbor Laboratory Press 2004
Aiheet:
Methods
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC509273/
https://ncbi.nlm.nih.gov/pubmed/15289481
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.2570004
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