A Comprehensive Database Integrating Copy Number Variation Profile in Healthy Individuals and Human Cancer
碩士 === 國立臺灣大學 === 生醫電子與資訊學研究所 === 107 === Copy number variation (CNV) is a region with structural variation in which the genomic copy numbers (CN) differs when compared to the reference genome. It is classically defined as a genomic segment that consists of at least 1000 base pairs of sequence alter...
| Main Authors: | , |
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| Other Authors: | |
| Format: | Others |
| Language: | en_US |
| Published: |
2019
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| Online Access: | http://ndltd.ncl.edu.tw/handle/jgc479 |