HIVID: An efficient method to detect HBV integration using low coverage sequencing von Li, Weiyang, Zeng, Xi, Lee, Nikki P., Liu, Xiao, Chen, Shengpei, Guo, Bing, Yi, Shang, Zhuang, Xuehan, Chen, Fang, Wang, Guan, Poon, Ronnie T., Fan, Sheung Tat, Mao, Mao, Li, Yingrui, Li, Songgang, Wang, Jun, JianWang, Xu, Xun, Jiang, Hui, Zhang, Xiuqing

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Massively Parallel Sequencing for Chromosomal Abnormality Testing in Trophectoderm Cells of Human Blastocysts von XUYANG YIN, KE TAN, CHUN GONG, XUCHAO LI, CHUYU LIN, YA GAO, YU LIANG, XIN YI, FENG MU, LIJIAN ZHAO, HUANHUAN PENG, BO XIONG, VAJTA, Gabor, SHUOPING ZHANG, DEHUA CHENG, GUANGXIU LU, XIUQING ZHANG, GE LIN, WEI WANG, HUI JIANG, YUEQIU TAN, CHUNLEI ZHANG, FANG CHEN, SHENGPEI CHEN, CHUNSHENG ZHANG, XIAOYU PAN

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Noninvasive prenatal testing of trisomies 21 and 18 by massively parallel sequencing of maternal plasma DNA in twin pregnancies von Huang, Xuan, Zheng, Jing, Chen, Min, Zhao, Yangyu, Zhang, Chunlei, Liu, Lifu, Xie, Weiwei, Shi, Shuqiong, Wei, Yuan, Lei, Dongzhu, Xu, Chenming, Wu, Qichang, Guo, Xiaoling, Shi, Xiaomei, Zhou, Yi, Liu, Qiufang, Gao, Ya, Jiang, Fuman, Zhang, Hongyun, Su, Fengxia, Ge, Huijuan, Li, Xuchao, Pan, Xiaoyu, Chen, Shengpei, Chen, Fang, Fang, Qun, Jiang, Hui, Lau, Tze Kin, Wang, Wei

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A single cell level based method for copy number variation analysis by low coverage massively parallel sequencing von Zhang, Chunlei, Zhang, Chunsheng, Chen, Shengpei, Yin, Xuyang, Pan, Xiaoyu, Lin, Ge, Tan, Yueqiu, Tan, Ke, Xu, Zhengfeng, Hu, Ping, Li, Xuchao, Chen, Fang, Xu, Xun, Li, Yingrui, Zhang, Xiuqing, Jiang, Hui, Wang, Wei

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Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing von Tan, Yueqiu, Yin, Xuyang, Zhang, Shuoping, Jiang, Hui, Tan, Ke, Li, Jian, Xiong, Bo, Gong, Fei, Zhang, Chunlei, Pan, Xiaoyu, Chen, Fang, Chen, Shengpei, Gong, Chun, Lu, Changfu, Luo, Keli, Gu, Yifan, Zhang, Xiuqing, Wang, Wei, Xu, Xun, Vajta, Gábor, Bolund, Lars, Yang, Huanming, Lu, Guangxiu, Du, Yutao, Lin, Ge

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PSCC: sensitive and reliable population-scale copy number variation detection method based on low coverage sequencing von Li, Xuchao, Chen, Shengpei, Xie, Weiwei, Vogel, Ida, Choy, Kwong Wai, Chen, Fang, Christensen, Rikke, Zhang, Chunlei, Ge, Huijuan, Jiang, Haojun, Yu, Chang, Huang, Fang, Wang, Wei, Jiang, Hui, Zhang, Xiuqing

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Performance comparison between rapid sequencing platforms for ultra-low coverage sequencing strategy von Chen, Shengpei, Li, Sheng, Xie, Weiwei, Li, Xuchao, Zhang, Chunlei, Jiang, Haojun, Zheng, Jing, Pan, Xiaoyu, Zheng, Hancheng, Liu, Jia Sophie, Deng, Yongqiang, Chen, Fang, Jiang, Hui

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Noninvasive prenatal detection for pathogenic CNVs: the application in α-thalassemia von Ge, Huijuan, Huang, Xuan, Li, Xuchao, Chen, Shengpei, Zheng, Jing, Jiang, Haojun, Zhang, Chunlei, Pan, Xiaoyu, Guo, Jing, Chen, Fang, Chen, Ning, Fang, Qun, Jiang, Hui, Wang, Wei

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Prenatal detection of aneuploidy and imbalanced chromosomal arrangements by massively parallel sequencing von Dan, Shan, Chen, Fang, Choy, Kwong Wai, Jiang, Fuman, Lin, Jingrong, Xuan, Zhaoling, Wang, Wei, Chen, Shengpei, Li, Xuchao, Jiang, Hui, Leung, Tak Yeung, Lau, Tze Kin, Su, Yue, Zhang, Weiyuan, Zhang, Xiuqing

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Effective noninvasive zygosity determination by maternal plasma target region sequencing von Zheng, Jing, Xu, Chenming, Guo, Jing, Wei, Yuan, Ge, Huijuan, Li, Xuchao, Zhang, Chunlei, Jiang, Haojun, Pan, Ling, Tang, Weiping, Xie, Weiwei, Zhang, Hongyun, Zhao, Yangyu, Jiang, Fuman, Chen, Shengpei, Wang, Wei, Xu, Xun, Chen, Fang, Huang, Hefeng, Jiang, Hui

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Electrochemically shape-controlled synthesis of trapezohedral platinum nanocrystals with high electrocatalytic activity von Li, Yanyan, Jiang, Yanxia, Chen, Minghui, Liao, Honggang, Huang, Rui, Zhou, Zhiyou, Tian, Na, Chen, Shengpei, Sun, Shigang

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Kinetics of oxygen reduction over Sm0.5Sr0.5CoO3 supported on La0.9Sr0.1Ga0.8Mg0.2O3 von Wang, Shizhong, Chen, Tong, Chen, Shengpei

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Whole-genome sequencing identifies recurrent mutations in hepatocellular carcinoma von Kan, Zhengyan, Zheng, Hancheng, Liu, Xiao, Li, Shuyu, Barber, Thomas D, Gong, Zhuolin, Gao, Huan, Hao, Ke, Willard, Melinda D, Xu, Jiangchun, Hauptschein, Robert, Rejto, Paul A, Fernandez, Julio, Wang, Guan, Zhang, Qinghui, Wang, Bo, Chen, Ronghua, Wang, Jian, Lee, Nikki P, Zhou, Wei, Lin, Zhao, Peng, Zhiyu, Yi, Kang, Chen, Shengpei, Li, Lin, Fan, Xiaomei, Yang, Jie, Ye, Rui, Ju, Jia, Wang, Kai, Estrella, Heather, Deng, Shibing, Wei, Ping, Qiu, Ming, Wulur, Isabella H, Liu, Jiangang, Ehsani, Mariam E, Zhang, Chunsheng, Loboda, Andrey, Sung, Wing Kin, Aggarwal, Amit, Poon, Ronnie T, Fan, Sheung Tat, Wang, Jun, Hardwick, James, Reinhard, Christoph, Dai, Hongyue, Li, Yingrui, Luk, John M, Mao, Mao

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A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing von Chen, Shengpei, Lau, Tze Kin, Zhang, Chunlei, Xu, Chenming, Xu, Zhengfeng, Hu, Ping, Xu, Jian, Huang, Hefeng, Pan, Ling, Jiang, Fuman, Chen, Fang, Pan, Xiaoyu, Xie, Weiwei, Liu, Ping, Li, Xuchao, Zhang, Lei, Li, Songgang, Li, Yingrui, Xu, Xun, Wang, Wei, Wang, Jun, Jiang, Hui, Zhang, Xiuqing

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Haplotype-based approach for noninvasive prenatal diagnosis of congenital adrenal hyperplasia by maternal plasma DNA sequencing von Ma, Dingyuan, Ge, Huijuan, Li, Xuchao, Jiang, Tao, Chen, Fang, Zhang, Yanyan, Hu, Ping, Chen, Shengpei, Zhang, Jingjing, Ji, Xiuqing, Xu, Xun, Jiang, Hui, Chen, Minfeng, Wang, Wei, Xu, Zhengfeng

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Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness von Meng, Meng, Li, Xuchao, Ge, Huijuan, Chen, Fang, Han, Mingyu, Zhang, Yanyan, Kang, Dongyang, Xie, Weiwei, Gao, Zhiying, Pan, Xiaoyu, Dai, Pu, Chi, Fanglu, Chen, Shengpei, Liu, Ping, Zhang, Chunlei, Cao, Jianjun, Jiang, Hui, Xu, Xun, Wang, Wei, Duan, Tao

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Kinetics of Oxygen Reduction over Sm[sub 0.5]Sr[sub 0.5]CoO[sub 3] Supported on La[sub 0.9]Sr[sub 0.1]Ga[sub 0.8]Mg[sub 0.2]O[sub 3] von Wang, Shizhong, Chen, Tong, Chen, Shengpei

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Embryo genome profiling by single-cell sequencing for preimplantation genetic diagnosis in a β-thalassemia family von Xu, Yanwen, Chen, Shengpei, Yin, Xuyang, Shen, Xiaoting, Pan, Xiaoyu, Chen, Fang, Jiang, Hui, Liang, Yu, Wang, Wei, Xu, Xun, Wang, Jian, Zhang, Xiuqing, Zhou, Canquan, Wang, Jun

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Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies von Jiang, Fuman, Ren, Jinghui, Chen, Fang, Zhou, Yuqiu, Xie, Jiansheng, Dan, Shan, Su, Yue, Xie, Jianhong, Yin, Baomin, Su, Wen, Zhang, Huakun, Wang, Wei, Chai, Xianghua, Lin, Linhua, Guo, Hui, Li, Qiyun, Li, Peipei, Yuan, Yuying, Pan, Xiaoyu, Li, Yihan, Liu, Lifu, Chen, Huifei, Xuan, Zhaoling, Chen, Shengpei, Zhang, Chunlei, Zhang, Hongyun, Tian, Zhongming, Zhang, Zhengyu, Jiang, Hui, Zhao, Lijian, Zheng, Weimou, Li, Songgang, Li, Yingrui, Wang, Jun, Wang, Jian, Zhang, Xiuqing

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Embryo Genome Profiling by Single-Cell Sequencing for Preimplantation Genetic Diagnosis in a [Beta]-Thalassemia Family von Xu, Yanwen, Chen, Shengpei, Yin, Xuyang, Shen, Xiaoting, Pan, Xiaoyu, Chen, Fang, Jiang, Hui, Liang, Yu, Wang, Wei, Xu, Xun, Wang, Jian, Zhang, Xiuqing, Zhou, Canquan, Wang, Jun

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