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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
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???jsp.browse.items-by-title.jump??? [ ???jsp.browse.general.jump2chinese??? ] [ ???jsp.browse.general.jump2numbers??? ] [ A B C D E F G H I J K L M N O P Q R S T U V W X Y Z ]
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Institution Date Title Author
臺大學術典藏 2020-07-03T08:28:35Z Haplotype frequencies of nine Y-chromosome STR loci in the Taiwanese Han population Tsai L.-C.;Yuen T.-Y.;Hsieh H.-M.;Lin M.;Tzeng C.-H.;Huang N.-E.;Linacre A.;James Chun-I Lee; Tsai L.-C.; Yuen T.-Y.; Hsieh H.-M.; Lin M.; Tzeng C.-H.; Huang N.-E.; Linacre A.; JAMES CHUN-I LEE
國立臺灣大學 2013 Haplotype Kernel Association Test as a Powerful Method to Identify Chromosomal Regions Harboring Uncommon Causal Variants Lin, Wan-Yu; Yi, Nengjun; Lou, Xiang-Yang; Zhi, Degui; Zhang, Kui; Gao, Guimin; Tiwari, Hemant K.; Liu, Nianjun; 林菀俞
臺大學術典藏 2018-09-10T09:41:02Z Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants Lin, Wan-Yu;Yi, Nengjun;Lou, Xiang-Yang;Zhi, Degui;Zhang, Kui;Gao, Guimin;Tiwari, Hemant K.;Liu, Nianjun; Lin, Wan-Yu; WAN-YU LIN; Yi, Nengjun; Lou, Xiang-Yang; Zhi, Degui; Zhang, Kui; Gao, Guimin; Tiwari, Hemant K.; Liu, Nianjun
臺大學術典藏 2022-05-04T09:10:39Z Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants WAN-YU LIN; Yi N.; Lou X.-Y.; Zhi D.; Zhang K.; Gao G.; Tiwari H.K.; Liu N.
中國醫藥大學 2010-06 Haplotype of BAK1 (BCL2 antagonist killer 1) polymorphisms associated with the risk of developing Kawasaki disease in Taiwanese children 黃毓銓(Yu-Chuen Huang);林應如(Ying-Ju Lin);張正成(Jeng-Sheng Chang);陳世殷(Shih-Yin, Chen);萬磊(Lei Wan);許晉銓(Jinn-Chyuan Sheu);賴志河(Chih-Ho Lai);林振文(Lin Cheng Wen);劉詩平(Shih-Ping Liu);蔡輔仁(Fuu-Jen Tsai)*
高雄醫學大學 2007 Haplotype Tag SNP Selection using Hybrid Algorithms  Yang, Cheng-Hong;Ho, Chang-Hsuan;谷德倫;張學偉 
高雄醫學大學 2008 Haplotype Tagging SNPs Selection Using Particle Swarm Optimization  Yang, Cheng-Hong;Ho, Chang-Hsuan;張學偉;Chuang , Li-Yeh
國立臺灣大學 2012 Haplotype-Based Methods for Detecting Uncommon Causal Variants With Common SNPs Lin, Wan-Yu; Yi, Nengjun; Zhi, Degui; Zhang, Kui; Gao, Guimin; Tiwari, Hemant K.; Liu, Nianjun; 林菀俞
臺大學術典藏 2022-05-04T09:10:40Z Haplotype-Based Methods for Detecting Uncommon Causal Variants With Common SNPs WAN-YU LIN; Yi N.; Zhi D.; Zhang K.; Gao G.; Tiwari H.K.; Liu N.
國家衛生研究院 2019-07 Haplotypes constructed by Whole exome sequencing to map and identify a novel disease-causing RP2 gene variant from a recessive X linked Retinities Pigmentosa family Ching, Y;Fan, W;Lin, W;Tsai, W;Hu, L;Huang, S;Chung, R

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