跳到主要导航 跳到搜索 跳到主要内容

Assessment of the cPAS-based BGISEQ-500 platform for metagenomic sequencing

  • Chao Fang
  • , Huanzi Zhong
  • , Yuxiang Lin
  • , Bing Chen
  • , Mo Han
  • , Huahui Ren
  • , Haorong Lu
  • , Jacob M. Luber
  • , Min Xia
  • , Wangsheng Li
  • , Shayna Stein
  • , Xun Xu
  • , Wenwei Zhang
  • , Radoje Drmanac
  • , Jian Wang
  • , Huanming Yang
  • , Lennart Hammarström
  • , Aleksandar D. Kostic
  • , Karsten Kristiansen
  • , Junhua Li
  • BGI-Shenzhen
  • University of Copenhagen
  • Harvard University
  • Joslin Diabetes Center
  • Dana-Farber Cancer Institute
  • Zhejiang University
  • Clinical University Hospital
  • South China University of Technology

科研成果: 期刊稿件 › 评论/辩论

166 引用 (Scopus)

摘要

Background: More extensive use of metagenomic shotgun sequencing in microbiome research relies on the development of high-throughput, cost-effective sequencing. Here we present a comprehensive evaluation of the performance of the new high-throughput sequencing platform BGISEQ-500 for metagenomic shotgun sequencing and compare its performance with that of 2 Illumina platforms. Findings: Using fecal samples from 20 healthy individuals, we evaluated the intra-platform reproducibility for metagenomic sequencing on the BGISEQ-500 platform in a setup comprising 8 library replicates and 8 sequencing replicates. Cross-platform consistency was evaluated by comparing 20 pairwise replicates on the BGISEQ-500 platform vs the Illumina HiSeq 2000 platform and the Illumina HiSeq 4000 platform. In addition, we compared the performance of the 2 Illumina platforms against each other. By a newly developed overall accuracy quality control method, an average of 82.45 million high-quality reads (96.06% of raw reads) per sample, with 90.56% of bases scoring Q30 and above, was obtained using the BGISEQ-500 platform. Quantitative analyses revealed extremely high reproducibility between BGISEQ-500 intra-platform replicates. Cross-platform replicates differed slightly more than intra-platform replicates, yet a high consistency was observed. Only a low percentage (2.02%-3.25%) of genes exhibited significant differences in relative abundance comparing the BGISEQ-500 and HiSeq platforms, with a bias toward genes with higher GC content being enriched on the HiSeq platforms. Conclusions: Our study provides the first set of performance metrics for human gut metagenomic sequencing data using BGISEQ-500. The high accuracy and technical reproducibility confirm the applicability of the new platform for metagenomic studies, though caution is still warranted when combining metagenomic data from different platforms.

源语言英语
页(从-至)1-8
页数8
期刊GigaScience
卷7
期3
DOI
出版状态已出版 - 1 3月 2018
已对外发布是

联合国可持续发展目标

此成果有助于实现下列可持续发展目标:

  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉

学术指纹

探究 'Assessment of the cPAS-based BGISEQ-500 platform for metagenomic sequencing' 的科研主题。它们共同构成独一无二的学术指纹。

引用此