OmicsLonDA (Omics Longitudinal Differential Analysis) is a statistical framework that provides robust identification of time intervals where omics features are significantly different between groups. OmicsLonDA is based on 5 main steps:
Install the latest version of OmicsLonDA from Bioconductor:
library(OmicsLonDA)
library(SummarizedExperiment)
## Load 10 simulated features and metadata
data("omicslonda_data_example")The measurment matrix represents count/intensity of features from an omic experiment. Columns represent various samples from different subjects longitudinally. Rows represent various features. Here is an example:
omicslonda_data_example$ome_matrix[1:5, 1:5]
#>           Sample_2  Sample_3  Sample_4  Sample_5 Sample_6
#> Feature_1 13.84393  7.976260  8.392602  7.511995 25.05878
#> Feature_2 17.35090 12.151211 12.758727 11.825749 28.55361
#> Feature_3 17.61570 13.617460 11.505888 13.906188 29.41523
#> Feature_4 17.63444 11.557786 11.081131 12.852518 28.61033
#> Feature_5 18.49954  9.642724 12.765664 11.103249 29.09817The metadata dataframe contains annotations for each sample. Most impotantly it should have at least: (a) “Subject”: which denote from which subject this sample is coming from, (b) “Group”: which represents which group this sample is from (eg., healthy, disease, etc), (c) “Time”: which represents the collection time of the corresponding sample. Here is an example:
assay(omicslonda_se_object_adjusted)[1:5, 1:5]
#>           Sample_2   Sample_3   Sample_4   Sample_5  Sample_6
#> Feature_1        0 -0.5513775 -0.5004965 -0.6113461 0.5933772
#> Feature_2        0 -0.3562154 -0.3074287 -0.3833650 0.4981392
#> Feature_3        0 -0.2574379 -0.4259317 -0.2364567 0.5127220
#> Feature_4        0 -0.4224943 -0.4646099 -0.3163138 0.4839143
#> Feature_5        0 -0.6515421 -0.3709867 -0.5105080 0.4529296omicslonda_test_object = omicslonda_se_object_adjusted[1,]
visualizeFeature(se_object = omicslonda_test_object, text = "Feature_1",
                 unit = "days", ylabel = "Normalized Count", 
                 col = c("blue", "firebrick"), prefix = tempfile())Visualize first feature
visualizeFeatureSpline(se_object = omicslonda_test_object, omicslonda_object = res, fit.method = "ssgaussian",
                        text = "Feature_1", unit = "days",
                        ylabel = "Normalized Count", 
                        col = c("blue", "firebrick"),
                        prefix = "OmicsLonDA_example")Fitted spline of the first feature
visualizeTestStatHistogram(omicslonda_object = res, text = "Feature_1", 
                                fit.method = "ssgaussian", prefix = tempfile())null distribution of the first feature’s statistic
visualizeArea(omicslonda_object = res, fit.method = "ssgaussian",
              text = "Feature_1", unit = "days", 
              ylabel = "Normalized Count", col =
                c("blue", "firebrick"), prefix = tempfile())Significant time intervals of feature 1
prefix = tempfile()
if (!dir.exists(prefix)){
        dir.create(file.path(prefix))
}
feature.summary = as.data.frame(do.call(cbind, res$details),
                                stringsAsFactors = FALSE)
write.csv(feature.summary, file = sprintf("%s/Feature_%s_Summary_%s.csv",
                                          prefix = prefix, text = "Feature_1", 
                                          fit.method = "ssgaussian"), row.names = FALSE)OmicsLonDA is under active research development. Please report any bugs/suggestions to Ahmed Metwally (ametwall@stanford.edu).