Detecting disease rare alleles using single SNPs in families and haplotyping in unrelated subjects from the Genetic Analysis Workshop 17 data

Documenti analoghi

• Microsatellite linkage analysis, single-nucleotide polymorphisms, and haplotype associations with ECB21 in the COGA data
  di: Kraja, Aldi T, et al.
  Pubblicazione: (2005)
• Methods for adjusting population structure and familial relatedness in association test for collective effect of multiple rare variants on quantitative traits
  di: Zhang, Qunyuan, et al.
  Pubblicazione: (2011)
• A framework for analyzing both linkage and association: an analysis of Genetic Analysis Workshop 16 simulated data
  di: Daw, E Warwick, et al.
  Pubblicazione: (2009)
• Use of a random coefficient regression (RCR) model to estimate growth parameters
  di: Corbett, Jonathan, et al.
  Pubblicazione: (2003)
• The Genetic Analysis Workshop 16 Problem 3: simulation of heritable longitudinal cardiovascular phenotypes based on actual genome-wide single-nucleotide polymorphisms in the Framingham Heart Study
  di: Kraja, Aldi T, et al.
  Pubblicazione: (2009)