A method to screen gene variations that are associated with familial cancers based on the next generation exome sequencing data
碩士 === 國立陽明大學 === 生物醫學資訊研究所 === 101 === In this study, I took advantage of exome sequencing technology to determine genetic variants that would cause hereditary cancers. The methods used in this study have three parts: preprocessing (mapping and quality assessment), filtering and consequence predict...
| Main Authors: | , |
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| Other Authors: | |
| Format: | Others |
| Language: | zh-TW |
| Published: |
2013
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| Online Access: | http://ndltd.ncl.edu.tw/handle/24640394375292814085 |