Copy Number Variation of UGT 2B Genes in Indian Families Using Whole Genome Scans

Bohle, H. M., & Gabaldón, T. (2012). Selection of Marker Genes Using Whole-Genome DNA Polymorphism Analysis. Evolutionary Bioinformatics, (2012), 161-169. https://doi.org/10.4137/EBO.S8989
駱明瑜（2021）。Genetic Study in Previously Genetically Undiagnosed Patients: Next-generation Sequencing for TSC and Deafness〔碩士論文，國立臺灣大學〕。華藝線上圖書館。https://doi.org/10.6342/NTU202102458
Hicks, C., Miele, L., Koganti, T., Gaylor, L. Y., Rogers, D., Vijayakumar, V., & Megason, G. (2013). Analysis of Patterns of Gene Expression Variation within and between Ethnic Populations in Pediatric B-ALL. Cancer Informatics, (2013), 155-173. https://doi.org/10.4137/CIN.S11831
Chang, L. C., Das, B., Lih, C. J., Si, H., Camalier, C. E., III, P. M. M., & Polley, E. (2016). RefCNV: Identification of Gene-Based Copy Number Variants Using Whole Exome Sequencing. Cancer Informatics, (2016), 65-71. https://doi.org/10.4137/CIN.S36612
張凱欣（2016）。Whole-Genome Sequencing and Phenotypic Analysis of Bacillus subtilis F29-3〔碩士論文，長榮大學〕。華藝線上圖書館。https://www.airitilibrary.com/Article/Detail?DocID=U0015-0507201612270100