Whole-Genome Sequencing of S. haemolyticus
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Corresponding Organization :
Other organizations : Zhuhai People's Hospital, Jinan University, First Affiliated Hospital of Jinan University
Variable analysis
- Whole-genome sequencing of the two strains of S. haemolyticus
- Genome assembly
- Whole-genome sequencing was performed using paired-end sequencing with Novaseq 6000 (Illumina, 2×150 bp paired-end reads) and long sequencing with PacBio Sequel IIe (Pacific Biosciences, 10–15 Kb insert whole-genome shotgun libraries)
- PacBio reads were assembled using the Hifiasm software version 0.13-r308 and Canu version 1.7
- The genome assembly was then polished using Pilon software version 1.22 using Illumina reads
- The assembled genomes of the two strains of S. haemolyticus were submitted to the National Center for Biotechnology Information (NCBI) GenBank database and annotated using the NCBI Prokaryotic Annotation Pipeline (PGAP)
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