Evidence map›Paper›PMID 38221534›Full record

ArticleScientific reports2024

Comparison of the DNBSEQ platform and Illumina HiSeq 2000 for bacterial genome assembly.

Tongyuan Hu, Jianwei Chen, Xiaoqian Lin, Wenxin He, Hewei Liang, Mengmeng Wang, Wenxi Li, Zhinan Wu, Mo Han, Xin Jin and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Overexpression of the Lipid Transfer Protein GenePlants (Basel, Switzerland) · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Tongyuan HuBGI Research, Shenzhen, 518083, China.
Jianwei ChenBGI Research, Shenzhen, 518083, China.
Xiaoqian LinBGI Research, Shenzhen, 518083, China.
Wenxin HeBGI Research, Shenzhen, 518083, China.
Hewei LiangBGI Research, Shenzhen, 518083, China.
Mengmeng WangBGI Research, Shenzhen, 518083, China.
Wenxi LiBGI Research, Shenzhen, 518083, China.
Zhinan WuBGI Research, Shenzhen, 518083, China.
Mo HanBGI Research, Shenzhen, 518083, China.
Xin JinBGI Research, Shenzhen, 518083, China.
Karsten KristiansenBGI Research, Shenzhen, 518083, China.
Liang XiaoBGI Research, Shenzhen, 518083, China.
Yuanqiang ZouBGI Research, Shenzhen, 518083, China. zouyuanqiang@genomics.cn.

Funding

National Natural Science Foundation of China 32100009Natural Science Foundation of Guangdong Province 2019B020230001Shenzhen Municipal Government of China XMHT20220104017
6 · The paper itself

Abstract

The Illumina HiSeq platform has been a commonly used option for bacterial genome sequencing. Now the BGI DNA nanoball (DNB) nanoarrays platform may provide an alternative platform for sequencing of bacterial genomes. To explore the impact of sequencing platforms on bacterial genome assembly, quality assessment, sequence alignment, functional annotation, mutation detection, and metagenome mapping, we compared genome assemblies based on sequencing of cultured bacterial species using the HiSeq 2000 and BGISEQ-500 platforms. In addition, simulated reads were used to evaluate the impact of insert size on genome assembly. Genome assemblies based on BGISEQ-500 sequencing exhibited higher completeness and fewer N bases in high GC genomes, whereas HiSeq 2000 assemblies exhibited higher N50. The majority of assembly assessment parameters, sequences of 16S rRNA genes and genomes, numbers of single nucleotide variants (SNV), and mapping to metagenome data did not differ significantly between platforms. More insertions were detected in HiSeq 2000 genome assemblies, whereas more deletions were detected in BGISEQ-500 genome assemblies. Insert size had no significant impact on genome assembly. Taken together, our results suggest that DNBSEQ platforms would be a valid substitute for HiSeq 2000 for bacterial genome sequencing.

Indexed as

DNAGenome, BacterialBacteriaHigh-Throughput Nucleotide SequencingRNA, Ribosomal, 16SSequence Analysis, DNADNARNA, Ribosomal, 16S

Identifiers

PMID38221534
PMCPMC10788345

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.