2020
DOI: 10.1016/j.biotechadv.2020.107537
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Library preparation for next generation sequencing: A review of automation strategies

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Cited by 114 publications
(102 citation statements)
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“…Understanding the genomic sequence of SARS-CoV-2 obtained from clinical specimens can help identify the COVID-19 pandemic origins, delineate transmission events, unravel clues to pathogenesis, and monitor viral evolution over time ( 404 408 ). Over the last few decades, DNA sequencing technologies have relied on modifications of Sanger sequencing, which was developed in the 1970s ( 409 ).…”
Section: Laboratory Methods For the Detection Of Sars-cov-2mentioning
confidence: 99%
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“…Understanding the genomic sequence of SARS-CoV-2 obtained from clinical specimens can help identify the COVID-19 pandemic origins, delineate transmission events, unravel clues to pathogenesis, and monitor viral evolution over time ( 404 408 ). Over the last few decades, DNA sequencing technologies have relied on modifications of Sanger sequencing, which was developed in the 1970s ( 409 ).…”
Section: Laboratory Methods For the Detection Of Sars-cov-2mentioning
confidence: 99%
“…Over the last few decades, DNA sequencing technologies have relied on modifications of Sanger sequencing, which was developed in the 1970s ( 409 ). While Sanger sequencing technology is still used for small sequences (∼0.5 to 1 kb) such as single-gene targets, next-generation sequencing (NGS) technologies have allowed sequencing to be performed as massively paralleled reactions, allowing rapid access to complete genomes at a scale and cost that are feasible for many laboratories ( 404 406 , 410 412 ). For SARS-CoV-2 genomes of <30 kb, high-quality sequences can readily be obtained with NGS directly from clinical specimens using strategies like amplicon enrichment or bait capture techniques to favor the sequencing of the viral targets ( 413 ).…”
Section: Laboratory Methods For the Detection Of Sars-cov-2mentioning
confidence: 99%
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“…Molecular phenotyping will thus become a crucial step in personalized medicine, and further exploration of pathophysiological diversity in diseases of the gut will greatly improve our ability to realize this personalized medicine. At the same time, single-cell techniques are evolving further, first of all, allowing for higher throughput and lower cost per sample ( 44 ). Other new developments in high-resolution transcriptome-wide technologies are capable to infer the spatial localization of the cells of which gene expression is measured, shedding more light on the functioning of the gut mucosa as an organ ( 45 , 46 ).…”
Section: Discussionmentioning
confidence: 99%
“…Similar approaches are required to push increased utilization of sequencing to support the COVID-19 pandemic. For instance, the complexity and labor-intensive nature of sample and library preparation workflow could limit the widespread adoption of sequencing [165][166][167]. Efforts towards the automation and integration of sample and library preparation steps will enable increased adoption of sequencing platforms for COVID-19 pandemic management.…”
Section: Sample Preparationmentioning
confidence: 99%