Method comparison for discovering copy number variation with next generation sequencing in whole genome
碩士 === 國立交通大學 === 統計學研究所 === 102 === Copy Number Variations(CNV) are structural rearrangements of the genome like deletions, duplications, inversions, and translocations. Typically, CNVs are detected by experimental tools such as array CGH. With the advance of next generation sequencing (NGS) techno...
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| Format: | Others |
| Language: | zh-TW |
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2014
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| Online Access: | http://ndltd.ncl.edu.tw/handle/28984344078922540915 |