Evaluation and integration of somatic copy number detection tools for whole-exome sequencing data
碩士 === 臺北醫學大學 === 醫學資訊研究所 === 104 === Copy Number Variations (CNVs) are a form of structural variation that manifest as amplifications, deletions, translocations, and insertions in the genome with segment size larger than 50 bp. Previous studies have reported that CNVs are associated with biological...
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| Format: | Others |
| Language: | zh-TW |
| Published: |
2016
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| Online Access: | http://ndltd.ncl.edu.tw/handle/v3rnqf |