Xuwen Wang, Zhili Chang, Yuqian Liu, Shenjie Wang, Xiaoyan Zhu, Yang Shao, Jiayin Wang
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引用次数: 0
Abstract
Copy number variation (CNV) is a crucial biomarker for many complex traits and diseases. Although numerous CNV detection tools are available, no single method consistently achieves optimal performance across diverse sequencing samples, as each tool has distinct advantages and limitations. Therefore, integrating the strengths of these tools to improve CNV detection accuracy is both a promising strategy and a significant challenge. To address this, we propose EMcnv, a novel deep ensemble framework based on meta-learning. EMcnv combines multiple CNV detection strategies through a three-step approach: (i) leveraging meta-learning and meta-path heterogeneous graphs, employing Relational Graph Convolutional Networks as a specific model within the Heterogeneous Graph Neural Networks framework to develop a probabilistic weight meta-model that ensembles various CNV detection strategies; (ii) assigning probabilistic weights to calls from different CNV detection tools and aggregating them into weighted CNV regions (CNVRs); (iii) refining Copy number variations based on weighted CNVRs. We conducted comprehensive experiments on both simulated and real sequencing data using benchmark datasets. The results demonstrate that EMcnv significantly outperforms popular existing methods, underscoring its superiority and importance in CNV detection. To support further research, the source code is available for academic use at https://github.com/Sherwin-xjtu/EMcnv.
期刊介绍:
Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data.
The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.