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| Content Provider | frontiers |
|---|---|
| Author | Liu, Guojun Yang, Hongzhi Yuan, Xiguo |
| Abstract | Copy number variation (CNV) is one of the main structural variations in the human genome and accounts for a considerable proportion of variations. As CNVs can directly or indirectly cause cancer, mental illness, and genetic disease in humans, their effective detection in humans is of great interest in the fields of oncogene discovery, clinical decision-making, bioinformatics, and drug discovery. The advent of next-generation sequencing data makes CNV detection possible, and a large number of CNV detection tools are based on next-generation sequencing data. Due to the complexity (e.g., bias, noise, alignment errors) of next-generation sequencing data and CNV structures, the accuracy of existing methods in detecting CNVs remains low. In this work, we design a new CNV detection approach, called shortest path-based CNV (SPCNV), to improve the detection accuracy of CNVs. SPCNV calculates the k nearest neighbors of each read depth (RD) and defines the shortest path, shortest path relation, and shortest path cost sets based on which further calculates the mean shortest path cost of each RD and its k nearest neighbors. We utilize the ratio between the mean shortest path cost for each RD and the mean of the mean shortest path cost of its k nearest neighbors to construct a relative shortest path score formula that is able to determine a score for each RD. Based on the score profile, a boxplot is then applied to predict CNVs. The performance of the proposed method is verified by simulation data experiments and compared against several popular methods of the same type. Experimental results show that the proposed method achieves the best balance between recall and precision in each set of simulated samples. To further verify the performance of the proposed method in real application scenarios, we then select real sample data from the 1000 Genomes Project to conduct experiments. The proposed method achieves the best F1-scores in almost all samples. Therefore, the proposed method can be used as a more reliable tool for the routine detection of CNVs. |
| ISSN | 16648021 |
| DOI | 10.3389/fgene.2022.1084974 |
| Volume Number | 13 |
| Journal | Frontiers in Genetics |
| Language | English |
| Publisher Date | 2023-01-17 |
| Access Restriction | Open |
| Subject Keyword | Next-generation sequencing data Copy number variation K nearest neighbors Read depth Shortest path |
| Content Type | Text |
| Resource Type | Article |
| Subject | Genetics Molecular Medicine Genetics (clinical) |
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