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Comparison between MGI and Illumina sequencing platforms for whole genome sequencing.
Jeon, Sol A; Park, Jong Lyul; Park, Seung-Jin; Kim, Jeong Hwan; Goh, Sung-Ho; Han, Ji-Youn; Kim, Seon-Young.
Afiliação
  • Jeon SA; Personalized Genomic Medicine Research Center, KRIBB, 34141, Daejeon, South Korea.
  • Park JL; Department of Bioscience, University of Science and Technology, 34113, Daejeon, South Korea.
  • Park SJ; Personalized Genomic Medicine Research Center, KRIBB, 34141, Daejeon, South Korea.
  • Kim JH; Personalized Genomic Medicine Research Center, KRIBB, 34141, Daejeon, South Korea.
  • Goh SH; Department of Bioscience, University of Science and Technology, 34113, Daejeon, South Korea.
  • Han JY; Personalized Genomic Medicine Research Center, KRIBB, 34141, Daejeon, South Korea.
  • Kim SY; National Cancer Center, Goyang-si, Republic of Korea.
Genes Genomics ; 43(7): 713-724, 2021 07.
Article em En | MEDLINE | ID: mdl-33864614
ABSTRACT

BACKGROUND:

Illumina next generation sequencing (NGS) systems are the major sequencing platform in worldwide next-generation sequencing market. On the other hand, MGI Tech launched a series of new NGS equipment that promises to deliver high-quality sequencing data faster and at lower prices than Illumina's sequencing instruments.

OBJECTIVE:

In this study, we compared the performance of the two platform's major sequencing instruments-Illumina's NovaSeq 6000 and MGI's MGISEQ-2000 and DNBSEQ-T7-to test whether the MGISEQ-2000 and DNBSEQ-T7 sequencing instruments are also suitable for whole genome sequencing.

METHODS:

We sequenced two pairs of normal and tumor tissues from Korean lung cancer patients using the three platforms. Then, we called single nucleotide variants (SNVs) and insertion and deletion (indels) for somatic and germline variants to compare the performance among the three platforms.

RESULTS:

In quality control analysis, all of the three platforms showed high-quality scores and deep coverages. Comparison among the three platforms revealed that MGISEQ-2000 is most concordant with NovaSeq 6000 for germline SNVs and indels, and DNBSEQ-T7 is most concordant with NovaSeq 6000 for somatic SNVs and indels.

CONCLUSIONS:

These results suggest that the performances of the MGISEQ-2000 and DNBSEQ-T7 platforms are comparable to that of the Illumina NovaSeq 6000 platform and support the potential applicability of the MGISEQ-2000 and DNBSEQ-T7 platforms in actual genome analysis fields.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sequenciamento de Nucleotídeos em Larga Escala / Sequenciamento Completo do Genoma Tipo de estudo: Evaluation_studies Limite: Humans Idioma: En Revista: Genes Genomics Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Coréia do Sul

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sequenciamento de Nucleotídeos em Larga Escala / Sequenciamento Completo do Genoma Tipo de estudo: Evaluation_studies Limite: Humans Idioma: En Revista: Genes Genomics Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Coréia do Sul