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  1. 1.   Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologies
  2. Talsania,Keyur; Shen,Tsai-Wei; Chen, Xiongfong; Jaeger, Erich; Li, Zhipan; Chen, Zhong; Chen, Wanqiu; Tran,Bao; Kusko, Rebecca; Wang, Limin; Pang, Andy Wing Chun; Yang, Zhaowei; Choudhari, Sulbha; Colgan, Michael; Fang, Li Tai; Carroll, Andrew; Shetty,Jyoti; Kriga,Yuliya; German,Oksana; Smirnova,Tatyana; Liu, Tiantain; Li, Jing; Kellman, Ben; Hong, Karl; Hastie, Alex R; Natarajan, Aparna; Moshrefi, Ali; Granat, Anastasiya; Truong, Tiffany; Bombardi, Robin; Mankinen, Veronnica; Meerzaman, Daoud; Mason, Christopher E; Collins, Jack; Stahlberg, Eric; Xiao, Chunlin; Wang, Charles; Xiao, Wenming; Zhao,Yongmei
  3. Genome Biology. 2022, Dec 13; 23(1): 255.
  1. 2.   Combined somatic mutation and copy number analysis in the survival of familial CLL
  2. Zhou, Weiyin; Goldin, Lynn; Wang, Mingyi; McMaster, Mary L; Jones, Kristine; Burdett, Laurie; Chanock, Stephen J; Yeager, Meredith; Dean, Michael; Caporaso, Neil E
  3. British Journal of Haematology. 2018, Jun; 181(5): 604-613.
  1. 3.   Mechanisms of copy number variation and hybrid gene formation in the KIR immune gene complex
  2. Traherne, J. A.; Martin, M.; Ward, R.; Ohashi, M.; Pellett, F.; Gladman, D.; Middleton, D.; Carrington, M.; Trowsdale, J.
  3. Human Molecular Genetics. 2010, Mar; 19(5): 737-751.
  1. 4.   MouseIndelDB: a database integrating genomic indel polymorphisms that distinguish mouse strains
  2. Akagi, K.; Stephens, R. M.; Li, J. F.; Evdokimov, E.; Kuehn, M. R.; Volfovsky, N.; Symer, D. E.
  3. Nucleic Acids Research. 2010, Jan; 38(Database issue): D600-D606.
  1. 5.   Prevalence in the United States of Selected Candidate Gene Variants
  2. Chang, M. H.; Lindegren, M. L.; Butler, M. A.; Chanock, S. J.; Dowling, N. F.; Gallagher, M.; Moonesinghe, R.; Moore, C. A.; Ned, R. M.; Reichler, M. R.; Sanders, C. L.; Welch, R.; Yesupriya, A.; Khoury, M. J.
  3. American Journal of Epidemiology. 2009 169(1): 54-66.
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