Publication:
Laboratory protocol for the digital multiplexed gene expression analysis of nasopharyngeal swab samples using the NanoString nCounter system.

dc.contributor.authorGarcía Aranda, Marilina
dc.contributor.authorLópez-Rodríguez, Inmaculada
dc.contributor.authorGarcía-Gutiérrez, Susana
dc.contributor.authorPadilla-Ruiz, Maria
dc.contributor.authorde Luque, Vanessa
dc.contributor.authorHortas, Maria Luisa
dc.contributor.authorDiaz, Tatiana
dc.contributor.authorÁlvarez, Martina
dc.contributor.authorBarragan-Mallofret, Isabel
dc.contributor.authorRedondo, Maximino
dc.contributor.authorResearch Network on Health Services in Chronic Diseases (Red de Investigación en Servicios Sanitarios y Enfermedades Crónicas, REDISSEC)
dc.date.accessioned2024-02-27T14:58:02Z
dc.date.available2024-02-27T14:58:02Z
dc.date.issued2022-02-02
dc.description.abstractThis paper describes a laboratory protocol to perform the NanoString nCounter Gene Expression Assay from nasopharyngeal swab samples.  It is urgently necessary to identify factors related to severe symptoms of respiratory infectious diseases, such as COVID-19, in order to assess the possibility of establishing preventive or preliminary therapeutic measures and to plan the services to be provided on hospital admission. At present, the samples recommended for microbiological diagnosis are those taken from the upper and/or the lower respiratory tract.  The NanoString nCounter Gene Expression Assay is a method based on the direct digital detection of mRNA molecules by means of target-specific, colour-coded probe pairs, without the need for mRNA conversion to cDNA by reverse transcription or the amplification of the resulting cDNA by PCR. This platform includes advanced analysis tools that reduce the need for bioinformatics support and also offers reliable sensitivity, reproducibility, technical robustness and utility for clinical application, even in RNA samples of low RNA quality or concentration, such as paraffin-embedded samples. Although the protocols for the analysis of blood or formalin-fixed paraffin-embedded samples are provided by the manufacturer, no corresponding protocol for the analysis of nasopharyngeal swab samples has yet been established. Therefore, the approach we describe could be adopted to determine the expression of target genes in samples obtained from nasopharyngeal swabs using the nCOUNTER technology.
dc.format.page133es_ES
dc.format.volume11es_ES
dc.identifier.doi10.12688/f1000research.103533.2
dc.identifier.e-issn2046-1402es_ES
dc.identifier.journalF1000Researches_ES
dc.identifier.otherhttp://hdl.handle.net/10668/21681
dc.identifier.pubmedID36329793es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/18595
dc.language.isoeng
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectDigital RNA quantification
dc.subjectImmunology
dc.subjectgene expression
dc.subjectnasopharyngeal swab
dc.subjectrespiratory infection
dc.subject.meshHumans
dc.subject.meshReproducibility of Results
dc.subject.meshDNA, Complementary
dc.subject.meshCOVID-19
dc.subject.meshRNA, Messenger
dc.subject.meshNasopharynx
dc.subject.meshGene Expression
dc.titleLaboratory protocol for the digital multiplexed gene expression analysis of nasopharyngeal swab samples using the NanoString nCounter system.
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication

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