DL-CNV: A deep learning method for identifying copy number variations based on next generation target sequencing
Copy number variations (CNVs) play an important role in many types of cancer. With the rapid development of next generation sequencing (NGS) techniques, many methods for detecting CNVs of a single sample have emerged: (ⅰ) require genome-wide data of both case and control samples, (ⅱ) depend on seque...
Main Authors: | , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
AIMS Press
2020-01-01
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Series: | Mathematical Biosciences and Engineering |
Subjects: | |
Online Access: | https://www.aimspress.com/article/doi/10.3934/mbe.2020011?viewType=HTML |