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Showing 157 - 169 of 524

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  • Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing

    Ann-Marie Patch, Katia Nones, Stephen H. Kazakoff, Felicity Newell, Scott Wood, Conrad Leonard, Oliver Holmes, Qinying Xu, Venkateswar Addala, Jenette Creaney, Bruce W. Robinson, Shujin Fu, Chunyu Geng, Tong Li, Wenwei Zhang, Xinming Liang, Junhua Rao, Jiahao Wang, Mingyu Tian, Yonggang Zhao, Fei Teng, Honglan Gou, Bicheng Yang, Hui Jiang, Feng Mu, John V. Pearson, Nicola Waddell

    published 10 Jan 2018

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  • Single molecule sequencing of the M13 virus genome without amplification

    Luyang Zhao, Liwei Deng, Gailing Li, Huan Jin, Jinsen Cai, Huan Shang, Yan Li, Haomin Wu, Weibin Xu, Lidong Zeng, Renli Zhang, Huan Zhao, Ping Wu, Zhiliang Zhou, Jiao Zheng, Pierre Ezanno, Andrew X. Yang, Qin Yan, Michael W. Deem, Jiankui He

    published 18 Dec 2017

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  • CELSR2 is a candidate susceptibility gene in idiopathic scoliosis

    Elisabet Einarsdottir, Anna Grauers, Jingwen Wang, Hong Jiao, Stefan A. Escher, Aina Danielsson, Ane Simony, Mikkel Andersen, Steen Bach Christensen, Kristina Åkesson, Ikuyo Kou, Anas M. Khanshour, Acke Ohlin, Carol Wise, Shiro Ikegawa, Juha Kere, Paul Gerdhem

    published 14 Dec 2017

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  • Variant genotyping with gap filling

    Riku Walve, Leena Salmela, Veli Mäkinen

    published 08 Sep 2017

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