2018
DOI: 10.1016/j.cmi.2017.10.013
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Next-generation sequencing technologies and their application to the study and control of bacterial infections

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Cited by 397 publications
(302 citation statements)
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“…Table summarizes the most commonly used sequencing technologies in phylogenomics. For more details on these different technologies see the Beginner's Handbook of Next Generation Sequencing by Genohub (https://genohub.com/next-generation-sequencing-handbook/ ) (see also Ambardar, ; Besser et al ., , and references therein). Choosing the appropriate sequencing technology for a phylogenomic study has important effects on downstream workflows, especially in terms of read length, as library preparation in some phylogenomic techniques (e.g.…”
Section: What Is Phylogenomics?mentioning
confidence: 99%
“…Table summarizes the most commonly used sequencing technologies in phylogenomics. For more details on these different technologies see the Beginner's Handbook of Next Generation Sequencing by Genohub (https://genohub.com/next-generation-sequencing-handbook/ ) (see also Ambardar, ; Besser et al ., , and references therein). Choosing the appropriate sequencing technology for a phylogenomic study has important effects on downstream workflows, especially in terms of read length, as library preparation in some phylogenomic techniques (e.g.…”
Section: What Is Phylogenomics?mentioning
confidence: 99%
“…NGS technology is an effective approach for laboratory management and microbe monitoring [26]. In this study, we carried out a holistic assessment of the biological background in the environment of a microbiology laboratory.…”
Section: Discussionmentioning
confidence: 99%
“…The Sanger method ("first generation" technology) was the main sequencing technology used between 1975 and 2005 for microbial WGS [87]. It produces long (500-1000 bp), high-quality sequencing reads and has been regarded as the gold standard for sequencing DNA.…”
Section: Next Generation Sequencing Platformsmentioning
confidence: 99%
“…However, when both technologies are used in combination to close genomes, also known as hybrid sequencing, the short reads generate good quality contigs while the long reads can close the gaps that are between the contigs during scaffold assembly. For more information on the main sequencing platforms and their performance, refer to the brief summary (see Table 2; [87]) and the details [77,94,95] that are described in above cited excellent recent reviews.…”
Section: Next Generation Sequencing Platformsmentioning
confidence: 99%