Two-tailed RT-qPCR panel for quality control of circulating microRNA studies
Autor: | Lukas Valihrach, Lucia Urdzikova-Machova, Peter Androvic, Eva Rohlova, Nataliya Romanyuk, Mikael Kubista |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
Quality Control
0301 basic medicine Cost-Benefit Analysis media_common.quotation_subject lcsh:Medicine Computational biology Biology Real-Time Polymerase Chain Reaction Article 03 medical and health sciences 0302 clinical medicine microRNA Animals Humans Quality (business) Circulating MicroRNA lcsh:Science media_common Protocol (science) Multidisciplinary lcsh:R Data interpretation Healthy Volunteers Rats Technical performance 030104 developmental biology Feasibility Studies lcsh:Q Reagent Kits Diagnostic RNA extraction Sample collection Biomarkers 030217 neurology & neurosurgery |
Zdroj: | Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019) Scientific Reports |
ISSN: | 2045-2322 |
DOI: | 10.1038/s41598-019-40513-w |
Popis: | Circulating cell-free microRNAs are promising candidates for minimally invasive clinical biomarkers for the diagnosis, prognosis and monitoring of many human diseases. Despite substantial efforts invested in the field, the research so far has failed to deliver expected results. One of the contributing factors is general lack of agreement between various studies, partly due to the considerable technical challenges accompanying the workflow. Pre-analytical variables including sample collection, RNA isolation, and quantification are sources of bias that may hamper biological interpretation of the results. Here, we present a Two-tailed RT-qPCR panel for quality control, monitoring of technical performance, and optimization of microRNA profiling experiments from biofluid samples. The Two-tailed QC (quality control) panel is based on two sets of synthetic spike-in molecules and three endogenous microRNAs that are quantified with the highly specific Two-tailed RT-qPCR technology. The QC panel is a cost-effective way to assess quality of isolated microRNA, degree of inhibition, and erythrocyte contamination to ensure technical soundness of the obtained results. We provide assay sequences, detailed experimental protocol and guide to data interpretation. The application of the QC panel is demonstrated on the optimization of RNA isolation from biofluids with the miRNeasy Serum/Plasma Advanced Kit (Qiagen). |
Databáze: | OpenAIRE |
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