The qgg package was developed based on the hypothesis that certain regions on the genome, so-called genomic features, may be enriched for causal variants affecting the trait. Several genomic feature classes can be formed based on previous studies and different sources of information such as genes, chromosomes or biological pathways.
qgg provides an infrastructure for efficient processing of large-scale genetic and phenotypic data including core functions for:
- fitting linear mixed models
- construction of genomic relationship matrices
- estimating genetic parameters (heritability and correlation)
- genomic prediction
- single marker association analysis
- gene set enrichment analysis
qgg handles large-scale data by taking advantage of:
- multi-core processing using openMP
- multithreaded matrix operations implemented in BLAS libraries (e.g. OpenBLAS, ATLAS or MKL)
- fast and memory-efficient batch processing of genotype data stored in binary files (e.g. PLINK bedfiles)
The qgg package provides a range of genomic feature modeling approaches, including genomic feature best linear unbiased prediction (GFBLUP) models, implemented using likelihood or Bayesian methods. Multiple features and multiple traits can be included in these models and different genetic models (e.g. additive, dominance, gene by gene and gene by environment interactions) can be used. Further extensions include a weighted GFBLUP model using differential weighting of the individual genetic marker relationships. Marker set tests, which are computationally very fast, can be performed. These marker set tests allow the rapid analyses of different layers of genomic feature classes to discover genomic features potentially enriched for causal variants. Marker set tests can thus facilitate more accurate prediction models.
You can install qgg from CRAN with:
install.packages("qgg")
The most recent version of qgg
can be obtained from github:
library(devtools)
devtools::install_github("psoerensen/qgg")
Below is a set of tutorials used for the qgg package:
This tutorial provides a brief introduction to R package qgg using small
simulated data examples.
Practicals_brief_introduction
This tutorial provides an introduction to R package qgg using 1000G
data.
Practicals_1000G_tutorials
This tutorial provide a simple introduction to polygenic risk scoring
(PRS) of complex traits and diseases using simulated data. The practical
will be a mix of theoretical and practical exercises in R that are used
for illustrating/applying the theory presented in the corresponding
lecture notes on polygenic risk scoring.
Practicals_human_example
In this tutorial we will be analysing quantitative traits observed in a
mice population. The mouse data consist of phenotypes for traits related
to growth and obesity (e.g. body weight, glucose levels in blood),
pedigree information, and genetic marker data.
Practicals_mouse_example
Below is a set of notes for the quantitative genetic theory, statistical models and methods implemented in the qgg package:
Estimation of Genetic Predisposition
Estimation of Genetic Parameters
Best Linear Unbiased Prediction Models
REstricted Maximum Likelihood Methods
Bayesian Linear Regression Models
- Edwards SM, Thomsen B, Madsen P, Sørensen P. 2015. Partitioning of genomic variance reveals biological pathways associated with udder health and milk production traits in dairy cattle. Genet Sel Evol 47:60. doi:10.1186/s12711-015-0132-6
- Edwards SM, Sørensen IF, Sarup P, Mackay TFC, Sørensen P. 2016. Genomic prediction for quantitative traits is improved by mapping variants to gene ontology categories in Drosophila melanogaster. Genetics 203:1871–1883. doi:10.1534/genetics.116.187161
- Ehsani A, Janss L, Pomp D, Sørensen P. 2015. Decomposing genomic variance using information from GWA, GWE and eQTL analysis. Anim Genet 47:165–173. doi:10.1111/age.12396
- Fang L, Sahana G, Ma P, Su G, Yu Y, Zhang S, Lund MS, Sørensen P. 2017. Exploring the genetic architecture and improving genomic prediction accuracy for mastitis and milk production traits in dairy cattle by mapping variants to hepatic transcriptomic regions responsive to intra-mammary infection. Genet Sel Evol 49:1–18. doi:10.1186/s12711-017-0319-0
- Fang L, Sahana G, Su G, Yu Y, Zhang S, Lund MS, Sørensen P. 2017. Integrating sequence-based GWAS and RNA-seq provides novel insights into the genetic basis of mastitis and milk production in dairy cattle. Sci Rep 7:45560. doi:10.1038/srep45560
- Fang L, Sørensen P, Sahana G, Panitz F, Su G, Zhang S, Yu Y, Li B, Ma L, Liu G, Lund MS, Thomsen B. 2018. MicroRNA-guided prioritization of genome-wide association signals reveals the importance of microRNA-target gene networks for complex traits in cattle. Sci Rep 8:1–14. doi:10.1038/s41598-018-27729-y
- Ørsted M, Rohde PD, Hoffmann AA, Sørensen P, Kristensen TN. 2017. Environmental variation partitioned into separate heritable components. Evolution (N Y) 72:136–152. doi:10.1111/evo.13391
- Ørsted M, Hoffmann AA, Rohde PD, Sørensen P, Kristensen TN. 2018. Strong impact of thermal environment on the quantitative genetic basis of a key stress tolerance trait. Heredity (Edinb). doi:10.1038/s41437-018-0117-7
- Rohde PD, Krag K, Loeschcke V, Overgaard J, Sørensen P, Kristensen TN. 2016. A quantitative genomic approach for analysis of fitness and stress related traits in a Drosophila melanogaster model population. Int J Genomics 2016:1–11.
- Rohde PD, Demontis D, Cuyabano BCD, The GEMS Group, Børglum AD, Sørensen P. 2016. Covariance Association Test (CVAT) identify genetic markers associated with schizophrenia in functionally associated biological processes. Genetics 203:1901–1913. doi:10.1534/genetics.116.189498
- Rohde PD, Gaertner B, Ward K, Sørensen P, Mackay TFC. 2017. Genomic analysis of genotype-by-social environment interaction for Drosophila melanogaster. Genetics 206:1969–1984. doi:10.1534/genetics.117.200642/-/DC1.1
- Rohde PD, Østergaard S, Kristensen TN, Sørensen P, Loeschcke V, Mackay TFC, Sarup P. 2018. Functional validation of candidate genes detected by genomic feature models. G3 Genes, Genomes, Genet 8:1659–1668. doi:10.1534/g3.118.200082
- Sarup P, Jensen J, Ostersen T, Henryon M, Sørensen P. 2016. Increased prediction accuracy using a genomic feature model including prior information on quantitative trait locus regions in purebred Danish Duroc pigs. BMC Genet 17:11. doi:10.1186/s12863-015-0322-9
- Sørensen P, de los Campos G, Morgante F, Mackay TFC, Sorensen D. 2015. Genetic control of environmental variation of two quantitative traits of Drosophila melanogaster revealed by whole-genome sequencing. Genetics 201:487–497. doi:10.1534/genetics.115.180273
- Sørensen IF, Edwards SM, Rohde PD, Sørensen P. 2017. Multiple trait covariance association test identifies gene ontology categories associated with chill coma recovery time in Drosophila melanogaster. Sci Rep 7:2413. doi:10.1038/s41598-017-02281-3