guokai8 / o2plsda

Omics data integration with o2plsda

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o2plsda: Multiomics Data Integration

o2plsda Project Status: CRAN version Code Size:DOI

o2plsda provides functions to do O2PLS-DA analysis for multiple omics integration.The algorithm came from "O2-PLS, a two-block (X±Y) latent variable regression (LVR) method with an integral OSC filter" which published by Johan Trygg and Svante Wold at 2003. O2PLS is a bidirectional multivariate regression method that aims to separate the covariance between two data sets (it was recently extended to multiple data sets) (Löfstedt and Trygg, 2011; Löfstedt et al., 2012) from the systematic sources of variance being specific for each data set separately.

Cross-Validation

In order to avoid overfitting of the model, the optimal number of latent variables for each model structure was estimated using group-balanced MCCV. The package could use the group information when we select the best paramaters with cross-validation. In cross-validation (CV) one minimizes a certain measure of error over some parameters that should be determined a priori. Here, we have three parameters: (nc, nx, ny). A popular measure is the prediction error ||Y - \hat{Y}||, where \hat{Y} is a prediction of Y. In our case the O2PLS method is symmetric in X and Y, so we minimize the sum of the prediction errors: ||X - \hat{X}||+||Y - \hat{Y}||.

And we also calculate the the average Q^2 values:

Q^2 = 1 - err / Var_{total};

err = Var_{expected} - Var_{estimated};

Here nc should be a positive integer, and nx and ny should be non-negative. The best integers are then the minimizers of the prediction error.

The O2PLS-DA analysis was performed as described by Bylesjö et al. (2007); briefly, the O2PLS predictive variation [$TW^\top$, $UC^\top$] was used for a subsequent O2PLS-DA analysis. The Variable Importance in the Projection (VIP) value was calculated as a weighted sum of the squared correlations between the OPLS-DA components and the original variable.

Installation

library(devtools)
install_github("guokai8/o2plsda")

Examples

library(o2plsda)
set.seed(123)
# sample * values
X = matrix(rnorm(5000),50,100)
# sample * values
Y = matrix(rnorm(5000),50,100)
rownames(X) <- paste("S",1:50,sep="")
rownames(Y) <- paste("S",1:50,sep="")
colnames(X) <- paste("Gene",1:100,sep="")
colnames(Y) <- paste("Lipid",1:100,sep="")
X = scale(X, scale=T)
Y = scale(Y, scale=T)
## group factor could be omitted if you don't have any group 
group <- rep(c("Ctrl","Treat"),each = 25)

Do cross validation with group information

set.seed(123)
## nr_folds : cross validation k-fold (suggest 10)
## ncores : parallel paramaters for large datasets
cv <- o2cv(X,Y,1:5,1:3,1:3,group=group,nr_folds = 10)
#####################################
# The best paramaters are nc =  5 , nx =  3 , ny =  3 
#####################################
# The Qxy is  0.08222935  and the RMSE is:  2.030108 
#####################################

Then we can do the O2PLS analysis with nc = 5, nx = 3, ny =3. You can also select the best paramaters by looking at the cross validation results.

fit <- o2pls(X,Y,5,3,3)
summary(fit)
######### Summary of the O2PLS results #########
### Call o2pls(X, Y, nc= 5 , nx= 3 , ny= 3 ) ###
### Total variation 
### X: 4900 ; Y: 4900  ###
### Total modeled variation ### X: 0.286 ; Y: 0.304  ###
### Joint, Orthogonal, Noise (proportions) ###
#               X     Y
#Joint      0.176 0.192
#Orthogonal 0.110 0.112
#Noise      0.714 0.696
### Variation in X joint part predicted by Y Joint part: 0.906 
### Variation in Y joint part predicted by X Joint part: 0.908 
### Variation in each Latent Variable (LV) in Joint part: 
#      LV1     LV2     LV3     LV4     LV5
#X 181.764 179.595 191.210 152.174 157.819
#Y 229.308 204.829 175.926 173.382 155.934
### Variation in each Latent Variable (LV) in X Orthogonal part: 
#      LV1     LV2     LV3
#X 227.856 166.718 143.602
### Variation in each Latent Variable (LV) in Y Orthogonal part: 
#      LV1     LV2     LV3
#Y 225.833 166.231 157.976

Extract the loadings and scores from the fit results

Xl <- loadings(fit,loading="Xjoint")
Xs <- scores(fit,score="Xjoint")
plot(fit,type="score",var="Xjoint", group=group)
plot(fit,type="loading",var="Xjoint", group=group,repel=F,rotation=TRUE)

Do the OPLSDA based on the O2PLS results

res <- oplsda(fit,group, nc=5)
plot(res,type="score", group=group)
vip <- vip(res)
plot(res,type="vip", group = group, repel = FALSE,order=TRUE)

Note

The package is still under development.

Citation

If you like this package, please contact me for the citation.

Contact information

For any questions please contact guokai8@gmail.com or https://github.com/guokai8/o2plsda/issues

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Omics data integration with o2plsda

License:GNU General Public License v3.0


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