VAReporter: variant reporter for cancer research of massive parallel sequencing.

Huang, Po-Jung; Lee, Chi-Ching; Chiu, Ling-Ya; Huang, Kuo-Yang; Yeh, Yuan-Ming; Yang, Chia-Yu; Chiu, Cheng-Hsun; Tang, Petrus

Huang, Po-Jung; Lee, Chi-Ching; Chiu, Ling-Ya; Huang, Kuo-Yang; Yeh, Yuan-Ming; Yang, Chia-Yu; Chiu, Cheng-Hsun; Tang, Petrus.

Afiliação

Huang PJ; Department of Biomedical Sciences, Chang Gung University, Taoyuan, Taiwan.
Lee CC; Genomic Medicine Research Core Laboratory, Chang Gung Memorial Hospital, Linkou, Taiwan.
Chiu LY; Molecular Medicine Research Center, Chang Gung University, Taoyuan, Taiwan.
Huang KY; Department and Graduate Institute of Computer Science and Information Engineering, Chang Gung University, Taoyuan, Taiwan.
Yeh YM; Molecular Medicine Research Center, Chang Gung University, Taoyuan, Taiwan.
Yang CY; Graduate Institute of Pathology and Parasitology, National Defense Medical Center, Taipei, Taiwan.
Chiu CH; Molecular Medicine Research Center, Chang Gung University, Taoyuan, Taiwan.
Tang P; Molecular Medicine Research Center, Chang Gung University, Taoyuan, Taiwan.

BMC Genomics ; 19(Suppl 2): 86, 2018 May 09.

Article em En | MEDLINE | ID: mdl-29764369

Assuntos

Sequenciamento do Exoma/métodos; Sequenciamento de Nucleotídeos em Larga Escala/métodos; Mutação; Neoplasias/genética; Algoritmos; Predisposição Genética para Doença; Humanos; Internet; Anotação de Sequência Molecular; Medicina de Precisão; Fluxo de Trabalho

Palavras-chave

Exomes; ICGC; NGS; SNV annotation; TCGA

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sequenciamento de Nucleotídeos em Larga Escala / Sequenciamento do Exoma / Mutação / Neoplasias Tipo de estudo: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

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