Protocol to analyze circulating small non-coding RNAs by high-throughput RNA sequencing from human plasma samples
Summary: The identification and validation of circulating small non-coding RNA (sncRNA) as biomarkers for disease diagnosis, staging, and response to novel therapies is still a compelling challenge. Pre-analytical variables, such as storage temperature or blood hemolysis, and different analytical ap...
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doaj-2f21c355d0314f82b4392096e3d24d9a2021-09-19T04:59:52ZengElsevierSTAR Protocols2666-16672021-09-0123100606Protocol to analyze circulating small non-coding RNAs by high-throughput RNA sequencing from human plasma samplesGiuseppina E. Grieco0Guido Sebastiani1Daniela Fignani2Noemi Brusco3Laura Nigi4Caterina Formichi5Giada Licata6Marco Bruttini7Romina D’Aurizio8Chantal Mathieu9Conny Gysemans10Francesco Dotta11Diabetes Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Siena 53100, Italy; Fondazione Umberto Di Mario, c/o Toscana Life Sciences, Siena 53100, ItalyDiabetes Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Siena 53100, Italy; Fondazione Umberto Di Mario, c/o Toscana Life Sciences, Siena 53100, Italy; UOC Diabetologia, Azienda Ospedaliera Universitaria Senese, Siena 53100, Italy; Corresponding authorDiabetes Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Siena 53100, Italy; Fondazione Umberto Di Mario, c/o Toscana Life Sciences, Siena 53100, ItalyDiabetes Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Siena 53100, Italy; Fondazione Umberto Di Mario, c/o Toscana Life Sciences, Siena 53100, ItalyDiabetes Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Siena 53100, Italy; Fondazione Umberto Di Mario, c/o Toscana Life Sciences, Siena 53100, ItalyDiabetes Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Siena 53100, Italy; Fondazione Umberto Di Mario, c/o Toscana Life Sciences, Siena 53100, ItalyDiabetes Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Siena 53100, Italy; Fondazione Umberto Di Mario, c/o Toscana Life Sciences, Siena 53100, ItalyDiabetes Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Siena 53100, Italy; Tuscany Centre for Precision Medicine (CReMeP), Siena 53100, ItalyInstitute of Informatics and Telematics, National Research Council, 56124 Pisa, ItalyClinical and Experimental Endocrinology, KU Leuven, Leuven, BelgiumClinical and Experimental Endocrinology, KU Leuven, Leuven, BelgiumDiabetes Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Siena 53100, Italy; Fondazione Umberto Di Mario, c/o Toscana Life Sciences, Siena 53100, Italy; Tuscany Centre for Precision Medicine (CReMeP), Siena 53100, ItalySummary: The identification and validation of circulating small non-coding RNA (sncRNA) as biomarkers for disease diagnosis, staging, and response to novel therapies is still a compelling challenge. Pre-analytical variables, such as storage temperature or blood hemolysis, and different analytical approaches affect sncRNA stability, detection, and expression, resulting in discrepancies among studies. Here, we report a systematic standardized protocol to reproducibly analyze circulating sncRNAs, employing high-throughput sncRNA sequencing and qRT-PCR validation, from 200 μL of human plasma samples.For details on the use and execution of this protocol, please refer to Ventriglia et al. (2020), Sebastiani et al. (2017), and Dotta et al. (2018).http://www.sciencedirect.com/science/article/pii/S2666166721003130Sequence analysisSequencingRNAseqHigh Throughput ScreeningMolecular Biology |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Giuseppina E. Grieco Guido Sebastiani Daniela Fignani Noemi Brusco Laura Nigi Caterina Formichi Giada Licata Marco Bruttini Romina D’Aurizio Chantal Mathieu Conny Gysemans Francesco Dotta |
spellingShingle |
Giuseppina E. Grieco Guido Sebastiani Daniela Fignani Noemi Brusco Laura Nigi Caterina Formichi Giada Licata Marco Bruttini Romina D’Aurizio Chantal Mathieu Conny Gysemans Francesco Dotta Protocol to analyze circulating small non-coding RNAs by high-throughput RNA sequencing from human plasma samples STAR Protocols Sequence analysis Sequencing RNAseq High Throughput Screening Molecular Biology |
author_facet |
Giuseppina E. Grieco Guido Sebastiani Daniela Fignani Noemi Brusco Laura Nigi Caterina Formichi Giada Licata Marco Bruttini Romina D’Aurizio Chantal Mathieu Conny Gysemans Francesco Dotta |
author_sort |
Giuseppina E. Grieco |
title |
Protocol to analyze circulating small non-coding RNAs by high-throughput RNA sequencing from human plasma samples |
title_short |
Protocol to analyze circulating small non-coding RNAs by high-throughput RNA sequencing from human plasma samples |
title_full |
Protocol to analyze circulating small non-coding RNAs by high-throughput RNA sequencing from human plasma samples |
title_fullStr |
Protocol to analyze circulating small non-coding RNAs by high-throughput RNA sequencing from human plasma samples |
title_full_unstemmed |
Protocol to analyze circulating small non-coding RNAs by high-throughput RNA sequencing from human plasma samples |
title_sort |
protocol to analyze circulating small non-coding rnas by high-throughput rna sequencing from human plasma samples |
publisher |
Elsevier |
series |
STAR Protocols |
issn |
2666-1667 |
publishDate |
2021-09-01 |
description |
Summary: The identification and validation of circulating small non-coding RNA (sncRNA) as biomarkers for disease diagnosis, staging, and response to novel therapies is still a compelling challenge. Pre-analytical variables, such as storage temperature or blood hemolysis, and different analytical approaches affect sncRNA stability, detection, and expression, resulting in discrepancies among studies. Here, we report a systematic standardized protocol to reproducibly analyze circulating sncRNAs, employing high-throughput sncRNA sequencing and qRT-PCR validation, from 200 μL of human plasma samples.For details on the use and execution of this protocol, please refer to Ventriglia et al. (2020), Sebastiani et al. (2017), and Dotta et al. (2018). |
topic |
Sequence analysis Sequencing RNAseq High Throughput Screening Molecular Biology |
url |
http://www.sciencedirect.com/science/article/pii/S2666166721003130 |
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