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DeepVariant-on-Spark: Small-Scale Genome Analysis Using a Cloud-Based Computing Framework.
Huang, Po-Jung; Chang, Jui-Huan; Lin, Hou-Hsien; Li, Yu-Xuan; Lee, Chi-Ching; Su, Chung-Tsai; Li, Yun-Lung; Chang, Ming-Tai; Weng, Sid; Cheng, Wei-Hung; Chiu, Cheng-Hsun; Tang, Petrus.
Afiliação
  • Huang PJ; Department of Biomedical Sciences, Chang Gung University, Taoyuan, Taiwan.
  • Chang JH; Graduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Lin HH; Genomic Medicine Core Laboratory, Chang Gung Memorial Hospital, Linkou, Taiwan.
  • Li YX; Graduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Lee CC; Institute of Bioinformatics and Structural Biology, National Tsing Hua University, Hsinchu, Taiwan.
  • Su CT; Graduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Li YL; Department of Computer Science and Information Engineering, Chang Gung University, Taoyuan, Taiwan.
  • Chang MT; Department of Biomedical Sciences, Chang Gung University, Taoyuan, Taiwan.
  • Weng S; ATGENOMIX INC, Rm. 918, 9F, 96, Chia Hsin Bldg. (Second Bldg.) Sec. 2, Zhongshan N. Rd., Zhongshan Dist., Taipei, Taiwan.
  • Cheng WH; Department of Biomedical Sciences, Chang Gung University, Taoyuan, Taiwan.
  • Chiu CH; ATGENOMIX INC, Rm. 918, 9F, 96, Chia Hsin Bldg. (Second Bldg.) Sec. 2, Zhongshan N. Rd., Zhongshan Dist., Taipei, Taiwan.
  • Tang P; Department of Biomedical Sciences, Chang Gung University, Taoyuan, Taiwan.
Comput Math Methods Med ; 2020: 7231205, 2020.
Article em En | MEDLINE | ID: mdl-32952600
Although sequencing a human genome has become affordable, identifying genetic variants from whole-genome sequence data is still a hurdle for researchers without adequate computing equipment or bioinformatics support. GATK is a gold standard method for the identification of genetic variants and has been widely used in genome projects and population genetic studies for many years. This was until the Google Brain team developed a new method, DeepVariant, which utilizes deep neural networks to construct an image classification model to identify genetic variants. However, the superior accuracy of DeepVariant comes at the cost of computational intensity, largely constraining its applications. Accordingly, we present DeepVariant-on-Spark to optimize resource allocation, enable multi-GPU support, and accelerate the processing of the DeepVariant pipeline. To make DeepVariant-on-Spark more accessible to everyone, we have deployed the DeepVariant-on-Spark to the Google Cloud Platform (GCP). Users can deploy DeepVariant-on-Spark on the GCP following our instruction within 20 minutes and start to analyze at least ten whole-genome sequencing datasets using free credits provided by the GCP. DeepVaraint-on-Spark is freely available for small-scale genome analysis using a cloud-based computing framework, which is suitable for pilot testing or preliminary study, while reserving the flexibility and scalability for large-scale sequencing projects.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Computação em Nuvem / Sequenciamento Completo do Genoma / Aprendizado Profundo Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Comput Math Methods Med Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Taiwan País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Computação em Nuvem / Sequenciamento Completo do Genoma / Aprendizado Profundo Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Comput Math Methods Med Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Taiwan País de publicação: Estados Unidos