Evidence map›Paper›PMID 32893860›Full record

ArticleGigaScience2020

TGS-GapCloser: A fast and accurate gap closer for large genomes with low coverage of error-prone long reads.

Mengyang Xu, Lidong Guo, Shengqiang Gu, Ou Wang, Rui Zhang, Brock A Peters, Guangyi Fan, Xin Liu, Xun Xu, Li Deng and 1 more

Open access · goldAbstract read
In one paragraph

Article in GigaScience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 340 papers.

0numbers the graph read from it
0cells of the map it votes in
340citing papers in PubMed
14.1field-weighted citation impact, top 1% of its field
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

340 citing papers in PubMed, 463 citations in OpenAlex.

  1. Article
  2. Article
  3. Whole genome ofMicrobiology resource announcements · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Chromosome-scale genome of European anchovy (Engraulis encrasicolus L., 1758) and comparative genomics uncover clupeid-specific immune gene expansions.DNA research : an international journal for rapid publication of reports on genes and genomes · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Draft genome sequence of hydrocarbon-utilizingMicrobiology resource announcements · 2026
    Article
  14. From screening to treatment:Microbiology spectrum · 2026
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

280 more citing papers are in PubMed but not listed here.

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

11 authors at 1 institution in 3 countries.

Mengyang XuBGI-Qingdao, BGI-Shenzhen, 2 Hengyunshan Road, West Coast New Area, Qingdao, 266426, China.
Lidong GuoBGI-Qingdao, BGI-Shenzhen, 2 Hengyunshan Road, West Coast New Area, Qingdao, 266426, China.
Shengqiang GuBGI-Qingdao, BGI-Shenzhen, 2 Hengyunshan Road, West Coast New Area, Qingdao, 266426, China.
Ou WangBGI-Shenzhen, Building 11, Beishan Industrial Zone, Yantian District, Shenzhen, 518083, China.
Rui ZhangBGI-Qingdao, BGI-Shenzhen, 2 Hengyunshan Road, West Coast New Area, Qingdao, 266426, China.
Brock A PetersBGI-Shenzhen, Building 11, Beishan Industrial Zone, Yantian District, Shenzhen, 518083, China.
Guangyi FanBGI-Qingdao, BGI-Shenzhen, 2 Hengyunshan Road, West Coast New Area, Qingdao, 266426, China.
Xin LiuBGI-Qingdao, BGI-Shenzhen, 2 Hengyunshan Road, West Coast New Area, Qingdao, 266426, China.
Xun XuBGI-Shenzhen, Building 11, Beishan Industrial Zone, Yantian District, Shenzhen, 518083, China.
Li DengBGI-Qingdao, BGI-Shenzhen, 2 Hengyunshan Road, West Coast New Area, Qingdao, 266426, China.
Yongwei ZhangBGI-Shenzhen, Building 11, Beishan Industrial Zone, Yantian District, Shenzhen, 518083, China.
BGI Group (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnalyses that use genome assemblies are critically affected by the contiguity, completeness, and accuracy of those assemblies. In recent years single-molecule sequencing techniques generating long-read information have become available and enabled substantial improvement in contig length and genome completeness, especially for large genomes (>100 Mb), although bioinformatic tools for these applications are still limited.

findingsWe developed a software tool to close sequence gaps in genome assemblies, TGS-GapCloser, that uses low-depth (∼10×) long single-molecule reads. The algorithm extracts reads that bridge gap regions between 2 contigs within a scaffold, error corrects only the candidate reads, and assigns the best sequence data to each gap. As a demonstration, we used TGS-GapCloser to improve the scaftig NG50 value of 3 human genome assemblies by 24-fold on average with only ∼10× coverage of Oxford Nanopore or Pacific Biosciences reads, covering with sequence data up to 94.8% gaps with 97.7% positive predictive value. These improved assemblies achieve 99.998% (Q46) single-base accuracy with final inserted sequences having 99.97% (Q35) accuracy, despite the high raw error rate of single-molecule reads, enabling high-quality downstream analyses, including up to a 31-fold increase in the scaftig NGA50 and up to 13.1% more complete BUSCO genes. Additionally, we show that even in ultra-large genome assemblies, such as the ginkgo (∼12 Gb), TGS-GapCloser can cover 71.6% of gaps with sequence data.

conclusionsTGS-GapCloser can close gaps in large genome assemblies using raw long reads quickly and cost-effectively. The final assemblies generated by TGS-GapCloser have improved contiguity and completeness while maintaining high accuracy. The software is available at https://github.com/BGI-Qingdao/TGS-GapCloser.

Indexed as

High-Throughput Nucleotide SequencingSoftwareComputational BiologyGenome, HumanHumansSequence Analysis, DNAgap closuregenome assemblyginkgoMHCthird-generation sequencing

Identifiers

PMID32893860
PMCPMC7476103
OpenAlexW3083775487

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.