Evidence map›Paper›PMID 35546658›Full record

ArticleBMC genomics2022

B-assembler: a circular bacterial genome assembler.

Fengyuan Huang, Li Xiao, Min Gao, Ethan J Vallely, Kevin Dybvig, T Prescott Atkinson, Ken B Waites, Zechen Chong

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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  3. Complete genome sequence ofMicrobiology resource announcements · 2024
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  4. Article
  5. Article
  6. Genomic Characterization of 2Pathogens & immunity · 2023
    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

8 authors at 1 institution in 1 country.

Fengyuan HuangInformatics Institute, Heersink School of Medicine, the University of Alabama at Birmingham, AL, 35294, Birmingham, USA.
Li XiaoDepartment of Medicine, Heersink School of Medicine, the University of Alabama at Birmingham, AB, 35294, Birmingham, USA.
Min GaoInformatics Institute, Heersink School of Medicine, the University of Alabama at Birmingham, AL, 35294, Birmingham, USA.
Ethan J VallelyInformatics Institute, Heersink School of Medicine, the University of Alabama at Birmingham, AL, 35294, Birmingham, USA.
Kevin DybvigDepartment of Genetics, Heersink School of Medicine, the University of Alabama at Birmingham, AL, 35294, Birmingham, USA.
T Prescott AtkinsonDepartment of Pediatrics, Heersink School of Medicine, the University of Alabama at Birmingham, AL, 35233, Birmingham, USA.
Ken B WaitesDepartment of Pathology, Heersink School of Medicine, the University of Alabama at Birmingham, AL, 35233, Birmingham, USA.
Zechen ChongInformatics Institute, Heersink School of Medicine, the University of Alabama at Birmingham, AL, 35294, Birmingham, USA. zchong@uab.edu.ORCID http://orcid.org/0000-0001-5750-1808
University of Alabama at Birmingham · US

Funding

NHLBI Data Stage Coordinating CenterOT3HL147154 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Ashok Kumar Krishnamurthy · 2018 to 2026
$98.9M
Structural variation analysis with and without a reference genomeR35GM138212 · NIGMS · UNIVERSITY OF VIRGINIA · PI Zechen Chong · 2020 to 2026
$2.6M
NHLBI NIH HHS 1OT3HL147154NHLBI NIH HHS OT3 HL147154NIGMS NIH HHS 1R35GM138212NIGMS NIH HHS R35 GM138212
6 · The paper itself

Abstract

backgroundAccurate bacteria genome de novo assembly is fundamental to understand the evolution and pathogenesis of new bacteria species. The advent and popularity of Third-Generation Sequencing (TGS) enables assembly of bacteria genomes at an unprecedented speed. However, most current TGS assemblers were specifically designed for human or other species that do not have a circular genome. Besides, the repetitive DNA fragments in many bacterial genomes plus the high error rate of long sequencing data make it still very challenging to accurately assemble their genomes even with a relatively small genome size. Therefore, there is an urgent need for the development of an optimized method to address these issues.

resultsWe developed B-assembler, which is capable of assembling bacterial genomes when there are only long reads or a combination of short and long reads. B-assembler takes advantage of the structural resolving power of long reads and the accuracy of short reads if applicable. It first selects and corrects the ultra-long reads to get an initial contig. Then, it collects the reads overlapping with the ends of the initial contig. This two-round assembling procedure along with optimized error correction enables a high-confidence and circularized genome assembly. Benchmarked on both synthetic and real sequencing data of several species of bacterium, the results show that both long-read-only and hybrid-read modes can accurately assemble circular bacterial genomes free of structural errors and have fewer small errors compared to other assemblers.

conclusionsB-assembler provides a better solution to bacterial genome assembly, which will facilitate downstream bacterial genome analysis.

Indexed as

Genome, BacterialHigh-Throughput Nucleotide SequencingBacteriaDNAHumansSequence Analysis, DNADNABacteria genomeDe novo assemblyHybrid-read assemblyLong-read-only assembly

Identifiers

PMID35546658
PMCPMC9092672
OpenAlexW4280563008

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.