Article
Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing.
PloS one - 1 Jan 2018
Patch Ann-Marie, Nones Katia, Kazakoff Stephen H, Newell Felicity, Wood Scott, Leonard Conrad, Holmes Oliver, Xu Qinying, Addala Venkateswar, Creaney Jenette, Robinson Bruce W, Fu Shujin, Geng Chunyu, Li Tong, Zhang Wenwei, Liang Xinming, Rao Junhua, Wang Jiahao, Tian Mingyu, Zhao Yonggang, Teng Fei, Gou Honglan, Yang Bicheng, Jiang Hui, Mu Feng, Pearson John V, Waddell Nicola
Abstract excerpt
Technological innovation and increased affordability have contributed to the widespread adoption of genome sequencing technologies in biomedical research. In particular large cancer research consortia have embraced next generation sequencing, and have used the technology to define the somatic mutation landscape of multiple cancer types. These studies have primarily utilised the Illumina HiSeq platforms. In this...
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