Inference of Chromosome-Specific Copy Number Using Population Haplotypes
碩士 === 國立中正大學 === 資訊工程所 === 98 === Large structural variations like deletions and duplications are quite common in the human populations. Among these structural variations, copy number variations (CNVs) often occupy regulatory regions of genes. Using array Comparative Genomic Hybridization (aCGH) pl...
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| Format: | Others |
| Language: | en_US |
| Published: |
2010
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| Online Access: | http://ndltd.ncl.edu.tw/handle/38084864300830968162 |