2016
DOI: 10.1128/genomea.01144-16
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Draft Genome Sequences of Five Clinical Strains of Brucella melitensis Isolated from Patients Residing in Kuwait

Abstract: Human brucellosis is a neglected and underrecognized infection of widespread geographic distribution. Brucellosis is present on all inhabited continents and endemic in many areas of the world, including Kuwait and the Middle East. Here, we present draft genome assemblies of five Brucella melitensis strains isolated from brucellosis patients in Kuwait.

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“…Fragmented DNA was processed through the steps of A-tailing, index ligation, and the addition of Illumina adapters at both the 5′ and 3′ ends of the DNA segments. The libraries were purified using the AMPure XP beads (Agencourt, Beckman Coulter Genomics) and quantified through qPCR (Life Technologies, Carlsbad, CA, USA) [ 39 ]. Post-normalization, the libraries were pooled and loaded at a 10.0 pM concentration on an Illumina NovaSeq 6000 platform (Illumina, San Diego) for 2 × 150 bp paired-end sequencing [ 36 ].…”
Section: Methodsmentioning
confidence: 99%
“…Fragmented DNA was processed through the steps of A-tailing, index ligation, and the addition of Illumina adapters at both the 5′ and 3′ ends of the DNA segments. The libraries were purified using the AMPure XP beads (Agencourt, Beckman Coulter Genomics) and quantified through qPCR (Life Technologies, Carlsbad, CA, USA) [ 39 ]. Post-normalization, the libraries were pooled and loaded at a 10.0 pM concentration on an Illumina NovaSeq 6000 platform (Illumina, San Diego) for 2 × 150 bp paired-end sequencing [ 36 ].…”
Section: Methodsmentioning
confidence: 99%
“…Briefly, 1000 ng of qualified DNA was sonicated to produce 350 bp fragments. These short DNA segments were then end-repaired, A-tailed, and subjected to index PCR [38]. Amplified libraries were purified through Agencourt AMPure XP magnetic beads (Beckman Coulter Genomics, Brea, CA, USA) and quantified through qPCR [39].…”
Section: Metagenomic Sequencingmentioning
confidence: 99%
“…Post-quality checks at BGI, the DNA was tagmented and subjected to library preparation. DNA fragments were end repaired, 3’A tailed and ligated with Illumina adapters ( Khan et al., 2016 ). Thereafter the libraries were purified through Agencourt AMPure XP magnetic beads (Beckman Coulter Genomics, Brea, CA, USA) ( Habibi et al., 2021 ).…”
Section: Methodsmentioning
confidence: 99%