Genome Association and Prediction Integrated Tools Version III
The DOI of GAPIT GitHub repository is: DOI: 10.5281/zenodo.7931838
If you use GAPIT and publish your analysis, please report the program version and cite the appropriate article:
The citation for GAPIT3 is:
Wang J., Zhang Z., GAPIT Version 3: Boosting Power and Accuracy for Genomic Association and Prediction, Genomics, Proteomics & Bioinformatics (2021), doi: https://doi.org/10.1016/j.gpb.2021.08.005.
The citation for GAPIT2 is:
Tang Y., Liu X., Wang J., Li M., Wang Q., et al., 2016 GAPIT Version 2: An Enhanced Integrated Tool for Genomic Association and Prediction. Plant J. 9, https://10.3835/plantgenome2015.11.0120.
The citation for GAPIT is:
Lipka A. E., Tian F., Wang Q., Peiffer J., Li M., et al., 2012 GAPIT: genome association and prediction integrated tool. Bioinformatics 28: 2397–2399, https://doi.org/10.1093/bioinformatics/bts444.
The citation for cBLUP and sBLUP is:
Wang J., Zhou Z., Zhang Z., Li H., Liu D., et al., 2018 Expanding the BLUP alphabet for genomic prediction adaptable to the genetic architectures of complex traits. Heredity https://doi.org/10.1038/s41437-018-0075-0.
The citation for BLINK is:
Huang M, Liu X, Zhou Y, Summers RM, Zhang Z. BLINK: A package for the next level of genome-wide association studies with both individuals and markers in the millions. Gigascience. https://doi.org/10.1093/gigascience/giy154.
The citation for Farm-CPU is:
Liu X., Huang M., Fan B., Buckler E. S., Zhang Z., 2016 Iterative Usage of Fixed and Random Effect Models for Powerful and Efficient Genome-Wide Association Studies. PLoS Genet. 12: e1005767. https://doi.org/10.1371/journal.pgen.1005767.
The citation for SUPER method is:
Wang Q., Tian F., Pan Y., Buckler E. S., Zhang Z., 2014 A SUPER Powerful Method for Genome Wide Association Study (Y Li, Ed.). PLoS One 9: e107684, https://doi.org/10.1371/journal.pone.0107684.
The citation for P3D is:
Zhang Z., Ersoz E., Lai C. Q., Todhunter R. J., Tiwari H. K., et al., 2010 Mixed linear model approach adapted for genome-wide association studies. Nat. Genet. 42: 355–360. https://doi.org/10.1038/ng.546.
Jiabo Wang and Zhiwu Zhang
[email protected] (Jiabo)
GAPIT is a package that is run in the R software environment. R can be freely downloaded from http://www.r-project.org. We also recommend the integrated development environment RStudio which is also freely available at http://www.rstudio.com.
GAPIT can currently be installed in several ways.
- From source on the internet
- From GitHub
- From an archive
GAPIT can be loaded with a single funciton.
R> source("http://zzlab.net/GAPIT/gapit_functions.txt")
Installation can also be made from GitHub when the R package devtools is available.
R> install.packages("devtools")
R> devtools::install_github("jiabowang/GAPIT", force=TRUE)
R> library(GAPIT)
or
R> install.packages("remotes")
R> remotes::install_github("jiabowang/GAPIT")
R> library(GAPIT)
Installation of same packages such as multtest and biobase can not be intalled from BiocManager. These packages can be downloaded in the Bioconductor website and be installed from local source files.
The website of Bioconductor is here:
https://bioconductor.org/packages/3.19/bioc/
GAPIT can be installed from an archive such as *.tar.gz or *.zip archive. An archive can be downloaded from the "releases" page. If you would like the latest version of GAPIT from the GitHub site you may want to clone it and then build it (this may require Rtools on Windows).
bash$ git clone [email protected]:jiabowang/GAPIT.git
bash$ R CMD build GAPIT
Once an archive has been obtained it can be installed from a shell, similar to as follows.
bash$ R CMD INSTALL GAPIT_3.2.0.9000.tar.gz
Or similarly from within R.
R> install.packages("GAPIT_3.2.0.9000.tar.gz", repos = NULL, type="source")
The user has the option of performing GWAS on multiple phenotypes in GAPIT. This is achieved by including all phenotypes in the text file of phenotypic data. Taxa names should be in the first column of the phenotypic data file and the remaining columns should contain the observed phenotype from each individual. Missing data should be indicated by either “NaN” or “NA”.
Hapmap is a commonly used format for storing sequence data where SNP information is stored in the rows and taxa information is stored in the columns. This format allows the SNP information (chromosome and position) and genotype of each taxa to be stored in one file.
GAPIT also accepts the numeric format. Homozygotes are denoted by “0” and “2” and heterozygotes are denoted by “1” in the “GD” file. Any numeric value between “0” and “2” can represent imputed SNP genotypes. The first row is a header file with SNP names, and the first column is the taxa name. The “GM” file contains the name and location of each SNP. The first column is the SNP id, the second column is the chromosome, and the third column is the base pair position. As seen in the example, the first row is a header file.
- GLM
The GAPIT uses Least Squares to solve the model. The GAPIT code for running a GLM is:
myGAPIT_GLM <- GAPIT(
Y=myY[,c(1,2)],
GD=myGD,
GM=myGM,
model="GLM",
PCA.total=5,
file.output=T
)
- MLM
EMMA method is used in GAPIT, the code of MLM is:
myGAPIT_MLM <- GAPIT(
Y=myY[,c(1,2)],
GD=myGD,
GM=myGM,
model="MLM",
PCA.total=5,
file.output=T
)
- CMLM
Compress Mixed Linear Model is published by Zhang in 2010. The code of CMLM is:
myGAPIT_CMLM <- GAPIT(
Y=myY[,c(1,2)],
GD=myGD,
GM=myGM,
model="CMLM",
PCA.total=5,
file.output=T
)
- MLMM
Multiple Loci Mixied linear Model is published by Segura in 2012. The code of MLMM in GAPIT is:
myGAPIT_MLMM <- GAPIT(
Y=myY[,c(1,2)],
GD=myGD,
GM=myGM,
model="MLMM",
PCA.total=5,
file.output=T
)
- SUPER
Settlement of MLM Under Progressively Exclusive Relation- ship is published by Qishan in 2014. The code of SUPER is:
myGAPIT_SUPER <- GAPIT(
Y=myY[,c(1,2)],
GD=myGD,
GM=myGM,
model="SUPER",
PCA.total=5,
file.output=T
)
- Farm-CPU
Fixed and random model Circulating Probability Unification (FarmCPU) is published by Xiaolei in 2016. The code of Farm-CPU in GAPIT is:
myGAPIT_FarmCPU <- GAPIT(
Y=myY[,c(1,2)],
GD=myGD,
GM=myGM,
model="FarmCPU",
PCA.total=5,
file.output=T
)
- gBLUP
gBLUP used marker kinship to replace the pedgree relationship matrix. The code is:
myGAPIT_gBLUP <- GAPIT(
Y=myY[,c(1,2)],
GD=myGD,
GM=myGM,
model="gBLUP",
PCA.total=5,
file.output=T
)
- cBLUP
cBLUP used group kinship to replace the individual matrix. The code is:
myGAPIT_cBLUP <- GAPIT(
Y=myY[,c(1,2)],
GD=myGD,
GM=myGM,
model="cBLUP",
PCA.total=5,
file.output=T
)
- sBLUP
sBLUP used SUPER method to build psedue QTN kinship matrix. The code is:
myGAPIT_sBLUP <- GAPIT(
Y=myY[,c(1,2)],
GD=myGD,
GM=myGM,
model="sBLUP",
PCA.total=5,
file.output=T
)
- MABLUP
MABLUP (Markers Assisted BLUP) used significant markers as fixed effect in the mixed linear model after GWAS. The GWAS method could be selected following model="". The buspred is used to predict GEBV after GWAS. The lmpred is used to select linear model or GBLUP method. The code is:
myGAPIT_MABLUP <- GAPIT(
Y=myY[,c(1,2)],
GD=myGD,
GM=myGM,
model="BLINK",
buspred=TRUE,
lmpred=FALSE,
PCA.total=5,
file.output=TRUE
)
Interactive Plots (links):
# loading packages for GAPIT and GAPIT functions
source("http://www.zzlab.net/GAPIT/gapit_functions.txt")
# loading data set
myY=read.table(file="http://zzlab.net/GAPIT/data/mdp_traits.txt", head = TRUE)
myGD=read.table("http://zzlab.net/GAPIT/data/mdp_numeric.txt",head=T)
myGM=read.table("http://zzlab.net/GAPIT/data/mdp_SNP_information.txt",head=T)
#myG=read.table(file="http://zzlab.net/GAPIT/data/mdp_genotype_test.hmp.txt", head = FALSE)
# performing simulation phenotype
set.seed(198521)
mysimulation<-GAPIT(h2=0.7,NQTN=20,GD=myGD,GM=myGM)
myY=mysimulation$Y
myGAPIT <- GAPIT(
Y=myY[,c(1,2)],
GD=myGD,
GM=myGM,
model=c("GLM","MLM","SUPER","MLMM","FarmCPU","Blink"),# choose model
#model=c("FarmCPU"),
PCA.total=3, # set total PCAs
NJtree.group=4, # set the number of clusting group in Njtree plot
QTN.position=mysimulation$QTN.position,
Inter.Plot=TRUE, # perform interactive plot
Multiple_analysis=TRUE, # perform multiple analysis
PCA.3d=TRUE, # plot 3d interactive PCA
file.output=T
)
Y = NULL, #phenotype
G = NULL, #hapmap genotype
GD = NULL, #numeric genotype
GM = NULL, #genotype map information
KI = NULL, #kinship
Z = NULL, #Z matrix for MLM, cMLM, encMLM
CV = NULL, #corvariance matrix
Aver.Dis=1000,
buspred = FALSE, #Prediction option for after GWAS MABLUP
bin.from = 10000, #SUPER
bin.to = 10000, #SUPER
bin.by = 10000, #SUPER
cutOff = 0.05, #threshold for significant
CV.Extragenetic = 0, # the top number of no-inheritance columns in CV
effectunit = 1, #Simulation phenotype
file.output = TRUE, #output option
FDRcut = FALSE, # filter pseudo QTN based on cutOff in blink
group.from = 1000000,#MLM
group.to = 1000000,#MLM
group.by = 50,#MLM
Geno.View.output = TRUE,#genotype analysis option
h2 = NULL, #simulation phenotype heritability
inclosure.from = 10, #SUPER
inclosure.to = 10, #SUPER
inclosure.by = 10, #SUPER
Inter.Plot = FALSE, #Interactive plot option
Inter.type = c("m","q"), #Interactive plot type for Manhattan and QQ plots
kinship.cluster = "average", #cMLM
kinship.group = 'Mean',#cMLM
kinship.algorithm = "Zhang",#cMLM
lmpred = FALSE, #option for linear model prediction or MABLUP prediction, that could be set as multiple parameters
model = "MLM",# model or method in GWAS or GS
maxOut = 100, # power for top number of markers in the GWAS
memo = NULL, #label for marking
Model.selection = FALSE,# optimum number of CV and PCAs
Multi_iter = FALSE, #Multiple step for FarmCPU and BLink
Major.allele.zero = FALSE, #convert hapmap file to numeric file, set major marker as 0
Multiple_analysis = TRUE, #option for multiple Manhattan and QQ plots
num_regwas = 10,# the max number of markers in second GWAS
NQTN = NULL, #Simulation phenotype, number of QTN
N.sig=NULL, #Random.model, Number of significant markers
NJtree.group = NULL, #NJtree set number of cluster group
NJtree.type = c("fan","unrooted"),#NJtree type
output.numerical = FALSE,# option for output numeric files
output.hapmap = FALSE, # option for output hapmap files
QTN.position = NULL, #Simulation phenotype, QTN position in the order of map file
QTNDist = "normal",
Random.model = TRUE, #Random.model to calculate PVE
sangwich.top = NULL, #SUPER
sangwich.bottom = NULL,#SUPER
SNP.P3D = TRUE,
SNP.effect = "Add",
SNP.impute = "Middle",
SNP.test = TRUE,
SNP.MAF = 0,
SNP.FDR = 1,
PCA.total = 0, # PCA number
PCA.col = NULL, #indicater colors for individuals in PCA plot
PCA.3d = FALSE, #3D PCA plot option
PCA.View.output = TRUE, #option for PCA plot
Phenotype.View= TRUE, # option for phenotype view plot