Addition of multiple rare SNPs to known common variants improves the association between disease and gene in the Genetic Analysis Workshop 17 data

Lignende værker

• A pathway-based association analysis model using common and rare variants
  af: Cheng, Lu, et al.
  Udgivet: (2011)
• Capability of common SNPs to tag rare variants
  af: Sun, Xiangqing, et al.
  Udgivet: (2011)
• Detecting disease rare alleles using single SNPs in families and haplotyping in unrelated subjects from the Genetic Analysis Workshop 17 data
  af: Kraja, Aldi T, et al.
  Udgivet: (2011)
• Challenges and directions: an analysis of Genetic Analysis Workshop 17 data by collapsing rare variants within family data
  af: Lin, Peng, et al.
  Udgivet: (2011)
• Evaluation of association tests for rare variants using simulated data sets in the Genetic Analysis Workshop 17 data
  af: Chen, Wenan, et al.
  Udgivet: (2011)