Data modeling as a main source of discrepancies in single and multiple marker association methods
Ledur, Mônica Corrêa (Universitat Autònoma de Barcelona. Departament de Ciència Animal i dels Aliments)
Navarro, Nicolas (Universitat Autònoma de Barcelona. Departament de Ciència Animal i dels Aliments)
Perez-Enciso, Miguel (Institució Catalana de Recerca i Estudis Avançats)

Fecha: 2009
Resumen: Genome-wide association studies have successfully identified several loci underlying complex diseases in humans. The development of high density SNP maps in domestic animal species should allow the detection of QTLs for economically important traits through association studies with much higher accuracy than traditional linkage analysis. Here we report the association analysis of the dataset simulated for the XII QTL-MAS meeting (Uppsala). We used two strategies, single marker association and haplotype-based association (Blossoc) that were applied to i) the raw data, and ii) the data corrected for infinitesimal, sex and generation effects. Both methods performed similarly in detecting the most strongly associated SNPs, about ten loci in total. The most significant ones were located in chromosomes 1, 4 and 5. Overall, the largest differences were found between corrected and raw data, rather than between single and multiple marker analysis. The use of raw data increased greatly the number of significant loci, but possibly also the rate of false positives. Bootstrap model aggregation removed most of discrepancies between adjusted and raw data when SMA was employed. Model choice should be carefully considered in genome-wide association studies.
Derechos: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. Creative Commons
Lengua: Anglès
Documento: Article ; recerca ; Versió publicada
Publicado en: BMC Proceedings, Vol. 3 (2 2009) , p. S9, ISSN 1753-6561

PMID: 19278548


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