- Home
- Featured Publications
- Center Publications
- Assessment of the cPAS-based BGISEQ-500 platform for metagenomic sequencing.
Assessment of the cPAS-based BGISEQ-500 platform for metagenomic sequencing.
Citation | “Assessment Of The Cpas-Based Bgiseq-500 Platform For Metagenomic Sequencing.”. Gigascience, pp. 1-8. . |
Center | Joslin Diabetes Center |
Author | 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 |
Abstract |
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. |
Year of Publication |
2018
|
Journal |
GigaScience
|
Volume |
7
|
Issue |
3
|
Number of Pages |
1-8
|
Date Published |
12/2018
|
ISSN Number |
2047-217X
|
DOI |
10.1093/gigascience/gix133
|
Alternate Journal |
Gigascience
|
PMID |
29293960
|
PMCID |
PMC5848809
|
Download citation |