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Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing.
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.
Afiliação
  • Patch AM; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Nones K; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Kazakoff SH; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Newell F; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Wood S; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Leonard C; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Holmes O; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Xu Q; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Addala V; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Creaney J; National Centre for Asbestos Related Disease, School of Medicine and Pharmacology, University of Western Australia, Nedlands, Western Australia, Australia.
  • Robinson BW; Department of Respiratory Medicine, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
  • Fu S; National Centre for Asbestos Related Disease, School of Medicine and Pharmacology, University of Western Australia, Nedlands, Western Australia, Australia.
  • Geng C; Department of Respiratory Medicine, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
  • Li T; BGI, BGI-Shenzhen, Shenzhen, China.
  • Zhang W; BGI, BGI-Shenzhen, Shenzhen, China.
  • Liang X; BGI, BGI-Shenzhen, Shenzhen, China.
  • Rao J; BGI, BGI-Shenzhen, Shenzhen, China.
  • Wang J; BGI, BGI-Shenzhen, Shenzhen, China.
  • Tian M; BGI, BGI-Shenzhen, Shenzhen, China.
  • Zhao Y; BGI, BGI-Shenzhen, Shenzhen, China.
  • Teng F; BGI, BGI-Shenzhen, Shenzhen, China.
  • Gou H; BGI, BGI-Shenzhen, Shenzhen, China.
  • Yang B; BGI, BGI-Shenzhen, Shenzhen, China.
  • Jiang H; BGI, BGI-Shenzhen, Shenzhen, China.
  • Mu F; BGI, BGI-Shenzhen, Shenzhen, China.
  • Pearson JV; BGI, BGI-Shenzhen, Shenzhen, China.
  • Waddell N; BGI, BGI-Shenzhen, Shenzhen, China.
PLoS One ; 13(1): e0190264, 2018.
Article em En | MEDLINE | ID: mdl-29320538
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 study we performed whole genome sequencing of three malignant pleural mesothelioma and matched normal samples using a new platform, the BGISEQ-500, and compared the results obtained with Illumina HiSeq X Ten. Germline and somatic, single nucleotide variants and small insertions or deletions were independently identified from data aligned human genome reference. The BGISEQ-500 and HiSeq X Ten platforms showed high concordance for germline calls with genotypes from SNP arrays (>99%). The germline and somatic single nucleotide variants identified in both sequencing platforms were highly concordant (86% and 72% respectively). These results indicate the potential applicability of the BGISEQ-500 platform for the identification of somatic and germline single nucleotide variants by whole genome sequencing. The BGISEQ-500 datasets described here represent the first publicly-available cancer genome sequencing performed using this platform.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genoma Humano / Sequenciamento de Nucleotídeos em Larga Escala / Células Germinativas Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Austrália País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genoma Humano / Sequenciamento de Nucleotídeos em Larga Escala / Células Germinativas Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Austrália País de publicação: Estados Unidos