- 學位論文
全基因體定序之變異偵測流程最佳化
Optimization of the Variant Calling Workflow for Whole Genome Sequencing
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並列摘要
參考文獻
[1] Crick, F. Central dogma of molecular biology. Nature 227, 561–563 (1970).
[2] 1000 Genomes Project Consortium. A global reference for human genetic variation. Nature 526, 68–74 (2015).
[3] The International SNP Map Working Group. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 409, 928–933 (2001).
[4] Mullaney, J.M. et al. Small insertions and deletions (INDELs) in human genomes. Hum. Mol. Genet. 19, R131–R136 (2010).
[5] Kennedy, G. C. et al. Large-scale genotyping of complex DNA. Nature Biotechnol. 21, 1233–1237 (2003).
延伸閱讀
- 張秀慧（2005）。遺傳連鎖分析之可調適全基因組掃描策略〔碩士論文，國立臺灣大學〕。華藝線上圖書館。https://doi.org/10.6342/NTU.2005.01142
- 周畹萍（2010）。視覺化基因分子調控路徑及基因附加資訊整合平台之建構〔碩士論文，臺北醫學大學〕。華藝線上圖書館。https://doi.org/10.6831/TMU.2010.00141
- 林佑任（2008）。依染色體績效進行突變之改良型基因演算法於非同步直序式超寬頻通訊系統多用戶偵測之應用研究〔碩士論文，國立臺北科技大學〕。華藝線上圖書館。https://doi.org/10.6841/NTUT.2008.00495
- Chiu, H. S. (2004). Identifying Significant Transcriptional Modules by Genetic Algorithms from Gene Expression Data [master's thesis, National Taiwan University]. Airiti Library. https://doi.org/10.6342/NTU.2004.00675
- zer, H. G., Usubalieva, I., Dorrance, D., Yilmaz, Y. E., Caligiuri, I., arcucci, G., & Huang, K. (2014). Identification of Medium-Sized Copy Number Alterations in Whole-Genome Sequencing. Cancer Informatics, (2014-S3), 105-111. https://doi.org/10.4137/CIN.S14023