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author | Peter Carbonetto | 2017-05-22 22:14:03 -0500 |
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committer | Peter Carbonetto | 2017-05-22 22:14:03 -0500 |
commit | 7616c7a019dc5996ab5d94c0822121a0e2060f99 (patch) | |
tree | 8c9bdf71628354b6eda11d6b30f0f50dd7b1e361 /README.md | |
parent | 7982ce46b0bf86bb7e0645242b11855cb783d6af (diff) | |
download | pangemma-7616c7a019dc5996ab5d94c0822121a0e2060f99.tar.gz |
Revised summary in README.md.
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@@ -1,39 +1,34 @@ +![Genetic associations discovered in CFW mice using GEMMA (Parker et al, +Nat. Genet., 2016)](cfw.gif) + # GEMMA: Genome-wide Efficient Mixed Model Association GEMMA is a software toolkit for fast application of linear mixed -models and related models to genome-wide association studies (GWAS) -and other large-scale data sets. - -![Genetic associations discovered in CFW mice using GEMMA (Parker et al, -Nat. Genet., 2016)](cfw.gif) +models (LMMs) and related models to genome-wide association studies +(GWAS) and other large-scale data sets. Features include: -+ Fast assocation tests implemented using the univariate linear mixed -model (LMM). In GWAS, this can correct for account for population -stratification and sample nonexchangeability. It also provides -estimates of the proportion of variance in phenotypes explained (PVE) -by available genotypes (often called "chip heritability" or "SNP -heritability"). - -+ Fast association tests for multiple phenotypes implemented using a -multivariate linear mixed model (lvLMM). - -It fits a multivariate linear mixed model (mvLMM) for testing marker -associations with multiple phenotypes simultaneously while controlling -for population stratification, and for estimating genetic correlations -among complex phenotypes. - -+ It fits a Bayesian sparse linear mixed model (BSLMM) using Markov -chain Monte Carlo (MCMC) for estimating PVE by typed genotypes, -predicting phenotypes, and identifying associated markers by jointly -modeling all markers while controlling for population structure. - -+ It estimates variance component/chip heritability, and partitions it -by different SNP functional categories. In particular, it uses HE -regression or REML AI algorithm to estimate variance components when -individual-level data are available. It uses MQS to estimate variance -components when only summary statisics are available. +1. Fast assocation tests implemented using the univariate linear mixed +model (LMM). In GWAS, this can correct for population structure and +sample nonexchangeability. It also provides estimates of the +proportion of variance in phenotypes explained by available genotypes +(PVE), often called "chip heritability" or "SNP heritability". + +2. Fast association tests for multiple phenotypes implemented using a +multivariate linear mixed model (lvLMM). In GWAS, this can correct for +populations tructure and sample nonexchangeability jointly in multiple +complex phenotypes. + +3 Bayesian sparse linear mixed model (BSLMM) for estimating PVE, +phenotype prediction, and multi-marker modeling in GWAS. + +4. Estimation of variance components ("chip heritability") partitioned +by different SNP functional categories from raw (individual-level) +data or summary data. For raw data, HE regression or the REML AI +algorithm can be used to estimate variance components when +individual-level data are available. For summary data, GEMMA uses the +MQS algorithm to estimate variance components. *Add note here about posting questions, comments or bug reports to Issues.* |