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OTG-snpcaller: an optimized pipeline based on TMAP and GATK for SNP calling from ion torrent data.
Zhu, Pengyuan; He, Lingyu; Li, Yaqiao; Huang, Wenpan; Xi, Feng; Lin, Lin; Zhi, Qihuan; Zhang, Wenwei; Tang, Y Tom; Geng, Chunyu; Lu, Zhiyuan; Xu, Xun.
Afiliação
  • Zhu P; BGI-Shenzhen, Shenzhen, China.
  • He L; BGI-Shenzhen, Shenzhen, China.
  • Li Y; BGI-Shenzhen, Shenzhen, China.
  • Huang W; BGI-Shenzhen, Shenzhen, China.
  • Xi F; BGI-Shenzhen, Shenzhen, China.
  • Lin L; BGI-Shenzhen, Shenzhen, China.
  • Zhi Q; BGI-Shenzhen, Shenzhen, China.
  • Zhang W; BGI-Shenzhen, Shenzhen, China.
  • Tang YT; Complete Genomics, Inc., Mountain View, California, United States of America.
  • Geng C; BGI-Shenzhen, Shenzhen, China.
  • Lu Z; BGI-Shenzhen, Shenzhen, China.
  • Xu X; BGI-Shenzhen, Shenzhen, China.
PLoS One ; 9(5): e97507, 2014.
Article em En | MEDLINE | ID: mdl-24824529
Because the new Proton platform from Life Technologies produced markedly different data from those of the Illumina platform, the conventional Illumina data analysis pipeline could not be used directly. We developed an optimized SNP calling method using TMAP and GATK (OTG-snpcaller). This method combined our own optimized processes, Remove Duplicates According to AS Tag (RDAST) and Alignment Optimize Structure (AOS), together with TMAP and GATK, to call SNPs from Proton data. We sequenced four sets of exomes captured by Agilent SureSelect and NimbleGen SeqCap EZ Kit, using Life Technology's Ion Proton sequencer. Then we applied OTG-snpcaller and compared our results with the results from Torrent Variants Caller. The results indicated that OTG-snpcaller can reduce both false positive and false negative rates. Moreover, we compared our results with Illumina results generated by GATK best practices, and we found that the results of these two platforms were comparable. The good performance in variant calling using GATK best practices can be primarily attributed to the high quality of the Illumina sequences.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Genoma Humano / Análise de Sequência de DNA / Polimorfismo de Nucleotídeo Único / Sequenciamento de Nucleotídeos em Larga Escala Idioma: En Ano de publicação: 2014 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Genoma Humano / Análise de Sequência de DNA / Polimorfismo de Nucleotídeo Único / Sequenciamento de Nucleotídeos em Larga Escala Idioma: En Ano de publicação: 2014 Tipo de documento: Article País de afiliação: China