Clover

Clover performs clustering-oriented de novo assembly of Illumina sequencing reads by combining de Bruijn graph methods with a k-mer clustering approach derived from the overlap-layout-consensus concept to improve robustness to sequencing errors, particularly when using large k-mers.


Key Features:

  • Clustering-oriented de novo assembly: groups k-mers during assembly to form clusters that guide contig construction.
  • De Bruijn graph methodology: uses de Bruijn graphs as the core graph-based assembly framework.
  • k-mer clustering (overlap-layout-consensus derived): integrates a k-mer clustering approach derived from overlap-layout-consensus concepts.
  • Robustness to sequencing errors and large k-mers: mitigates Illumina sequencing errors and supports use of large k-mer sizes.
  • Benchmarking metrics: reported improvements in corrected N50 and E-size metrics.
  • Comparative benchmarking: evaluated against ABySS, SOAPdenovo, SPAdes, Velvet, Bambus2, CABOG, MSR-CA, and SGA.
  • Datasets tested: validated on Staphylococcus aureus, Rhodobacter sphaeroides, human chromosome 14, Acinetobacter baumannii TYTH-1, and Morganella morganii KT.
  • Run time performance: maintained competitive run times in comparative evaluations.

Scientific Applications:

  • Microbial genome assembly: applied to bacterial genomes including Acinetobacter baumannii TYTH-1 and Morganella morganii KT.
  • Bacterial and eukaryotic assembly benchmarking: used for assembly of Staphylococcus aureus, Rhodobacter sphaeroides, and human chromosome 14.
  • Assembly performance evaluation: employed to improve and compare corrected N50 and E-size across assemblers.

Methodology:

Combines de Bruijn graph assembly with a k-mer clustering approach derived from overlap-layout-consensus concepts to reduce Illumina sequencing errors and enable use of large k-mers.

Topics

Details

Added:
1/18/2021
Last Updated:
2/12/2021

Operations

Publications

Hsieh M, Lu CL, Tang CY. Clover: a clustering-oriented de novo assembler for Illumina sequences. BMC Bioinformatics. 2020;21(1). doi:10.1186/s12859-020-03788-9. PMID:33203354. PMCID:PMC7672897.