2020
DOI: 10.1016/j.eimc.2020.02.006
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Uso de las tecnologías de secuenciación masiva para el diagnóstico y epidemiología de enfermedades infecciosas

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(1 citation statement)
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“…However, the development of massive whole genome sequencing techniques, based on next-generation sequencing (NGS) methods, allows millions to billions of DNA copies to be sequenced in a single run [12]. Despite its bioinformatics requirements, this methodology is gradually being incorporated into genomic studies in clinical care and epidemiological surveillance at a cost and scale hitherto inaccessible [13]. For the time being, its main application has been the characterization of the successive phenotypically and genotypically different SARS-CoV-2 variants that have emerged in recent months.…”
Section: Promotion Of Preventive Measuresmentioning
confidence: 99%
“…However, the development of massive whole genome sequencing techniques, based on next-generation sequencing (NGS) methods, allows millions to billions of DNA copies to be sequenced in a single run [12]. Despite its bioinformatics requirements, this methodology is gradually being incorporated into genomic studies in clinical care and epidemiological surveillance at a cost and scale hitherto inaccessible [13]. For the time being, its main application has been the characterization of the successive phenotypically and genotypically different SARS-CoV-2 variants that have emerged in recent months.…”
Section: Promotion Of Preventive Measuresmentioning
confidence: 99%