High-dimensional classification and feature selection tasks are ubiquitous with the recent advancement in data acquisition technology. In several application areas such as biology, genomics and proteomics, the data are often functional in their nature and exhibit a degree of roughness and non-stationarity. These structures pose additional challenges to commonly used methods that rely mainly on a two-stage approach performing variable selection and classification separately. We propose in this work a novel Gaussian process discriminant analysis (GPDA) that combines these steps in a unified framework. Our model is a two-layer non-stationary Gaussian process coupled with an Ising prior to identify differentially-distributed locations. Scalable inference is achieved via developing a variational scheme that exploits advances in the use of sparse inverse covariance matrices. We demonstrate the performance of our methodology on simulated datasets and two proteomics datasets: breast cancer and SARS-CoV-2. Our approach distinguishes itself by offering explainability as well as uncertainty quantification in addition to low computational cost, which are crucial to increase trust and social acceptance of data-driven tools.
翻译:在生物、基因组学和蛋白质组学等若干应用领域,数据的性质往往发挥作用,显示出一定程度的粗糙和非常态性。这些结构对通常使用的方法提出了额外的挑战,这些常用方法主要依赖一种两阶段方法,分别进行不同的选择和分类。我们在此工作中建议采用新的高森进程分布分析(GPDA),将这些步骤结合到一个统一的框架中。我们的模型是一个两层非静止的高斯进程,同时在确定不同分布地点之前采用Ising。通过制定一种变通办法,利用利用分散的反相异矩阵的使用进展,实现了可缩放的推断。我们展示了我们模拟数据集和两个蛋白质组数据集(乳腺癌和SARS-COV-2)的性能。我们的方法通过在低计算成本之外提供解释性和不确定性的量化来加以区分,这对于提高信任度和社会对数据驱动工具的接受度至关重要。