NSPA converts genetic variants of subjects into new values that capture how genetic variables interact with others to regulate a subject’s disease risk.

NSPA is written in Python 3. You need to download this repository to local and make sure the following packages have been installed.

• pandas
• numpy
• multiprocessing
• sklearn
• csv

Sample Run Command:

bash Run_BuildComprehensiveNetwork.sh

ComprehensiveNetwork.py contains one parameter indicating the dataset used to build the network. ComprehensiveNetwork.tsv is the output network. The first and second columns are SNP, the third column is information gain, and the fourth column is mutual infordmation. The resulting comprehensive network is fully connected, so some SNP interactions with weak interactions need to be filtered out.

Sample Run Command:

bash Run_BuildSubjectNetwork.sh

This command will produce a 5-fold cross-validation dataset with the transformed features. SubjectNetwork.py contains two parameters with the first parameter indicating the dataset and the second paramter indicating the edge list of the comprehensive network.

Although the first step has been parallelized using the multiprocessing package, if the dataset includes hundreds of thousands of SNPs, it is necessary to use high-performance computing to get the results in time. We propose to achieve high-performance computing by data chunking. The specific steps are.

1. partitioning the high-dimensional data into independent sub-datas by SNP, each sub-data including a less number of SNPs and labels.
2. evaluate all SNP interactions using ComprehensiveNetwork.py for each sub-data.
3. evaluate the feature interactions between any pair of sub-datas using /scr/ComprehensiveNetwork_Bipartisan.py.
4. merge. Note that the merged data can be very large. It is recommended that the weakest SNP interactions are removed before merging. This would reduce the overall data size by several orders of magnitude.

We have summarized the experiment procedures involved in the paper in the /Pipelines folder. A total of three experiments are involved.

1. Apply NSPA on synthetic datasets /Pipelines/1_SimulationStudy
2. Apply NSPA on GWAS data /Pipelines/2_NSPA
3. Overfitting study for GWAS /Pipelines/3_Overfitting

The input data corresponding to each study is stored in the /data folder, the results are in the /res folder, and the computational procedure is in the /scr folder.

You can reproduce our experiments by executing the .sh files sequentially. The parameters associated with each step are configurable at the top of the sh file. For privacy concerns, we cannot disclose the full GWAS data. Therefore, some of the experimental procedures cannot be replicated due to the lack of data. But you can still check out the different experimental results generated by different parameter configurations. File names in the /res folder distinguish the different experimental results.