Method comparison for discovering copy number variation with next-generation sequencing in target exome regions
碩士 === 國立交通大學 === 統計學研究所 === 102 === Exome sequencing using next-generation sequencing technologies is a cost-efficient approach for detection of disease variants. One of the important applications of exome sequencing data is to identify copy number variations (CNVs). During the last several years,...
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| Format: | Others |
| Language: | zh-TW |
| Published: |
2014
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| Online Access: | http://ndltd.ncl.edu.tw/handle/46254639984812006869 |