Genome-wide complex trait analysis (GCTA): methods, data analyses, and interpretations

Methods Mol Biol. 2013:1019:215-36. doi: 10.1007/978-1-62703-447-0_9.

Abstract

Estimating genetic variance is traditionally performed using pedigree analysis. Using high-throughput DNA marker data measured across the entire genome it is now possible to estimate and partition genetic variation from population samples. In this chapter, we introduce methods and a software tool called Genome-wide Complex Trait Analysis (GCTA) to estimate genomic relationships between pairs of conventionally unrelated individuals using genome-wide single nucleotide polymorphism (SNP) data, to estimate variance explained by all SNPs simultaneously on genomic or chromosomal segments or over the whole genome, and to perform a joint and conditional multiple SNPs association analysis using summary statistics from a meta-analysis of genome-wide association studies and linkage disequilibrium between SNPs estimated from a reference sample.

MeSH terms

  • Chromosomes, Human
  • Data Interpretation, Statistical
  • Genetic Markers
  • Genome, Human
  • Genome-Wide Association Study / statistics & numerical data*
  • Humans
  • Linkage Disequilibrium
  • Multifactorial Inheritance*
  • Pedigree*
  • Phenotype
  • Polymorphism, Single Nucleotide
  • Research Design
  • Software*

Substances

  • Genetic Markers