A Cluster-Based Approach for the Discovery of Copy Number Variations From Next-Generation Sequencing Data

The next-generation sequencing technology offers a wealth of data resources for the detection of copy number variations (CNVs) at a high resolution. However, it is still challenging to correctly detect CNVs of different lengths. It is necessary to develop new CNV detection tools to meet this demand....

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Bibliographic Details
Published inFrontiers in genetics Vol. 12; p. 699510
Main Authors Liu, Guojun, Zhang, Junying
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 28.06.2021
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Summary:The next-generation sequencing technology offers a wealth of data resources for the detection of copy number variations (CNVs) at a high resolution. However, it is still challenging to correctly detect CNVs of different lengths. It is necessary to develop new CNV detection tools to meet this demand. In this work, we propose a new CNV detection method, called CBCNV, for the detection of CNVs of different lengths from whole genome sequencing data. CBCNV uses a clustering algorithm to divide the read depth segment profile, and assigns an abnormal score to each read depth segment. Based on the abnormal score profile, Tukey's fences method is adopted in CBCNV to forecast CNVs. The performance of the proposed method is evaluated on simulated data sets, and is compared with those of several existing methods. The experimental results prove that the performance of CBCNV is better than those of several existing methods. The proposed method is further tested and verified on real data sets, and the experimental results are found to be consistent with the simulation results. Therefore, the proposed method can be expected to become a routine tool in the analysis of CNVs from tumor-normal matched samples.
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Edited by: Wei Lan, Guangxi University, China
This article was submitted to Computational Genomics, a section of the journal Frontiers in Genetics
Reviewed by: Ruifeng Hu, Harvard Medical School, United States; Cuncong Zhong, University of Kansas, United States
ISSN:1664-8021
1664-8021
DOI:10.3389/fgene.2021.699510