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Proposal of supervised data analysis strategy of plasma miRNAs fr | 53888
Journal of Clinical Trials

Journal of Clinical Trials
Open Access

ISSN: 2167-0870

+44 1478 350008

Proposal of supervised data analysis strategy of plasma miRNAs from hybridization array data with an application to assess hemolysis-related deregulation


2nd International Conference on Clinical Trials and Therapeutic Drug Monitoring

August 22-24, 2016 Philadelphia, USA

Elena Landoni

University of Milan, Italy
Fondazione IRCCS Istituto Nazionale dei Tumori, Italy

Scientific Tracks Abstracts: J Clin Trials

Abstract :

Background: Plasma miRNAs have the potential as cancer biomarkers but no consolidated guidelines for data mining in this field are available. The purpose of the study was to apply a supervised data analysis strategy in a context where prior knowledge is available, i.e. that of hemolysis-related miRNAs deregulation, so as to compare our results with existing evidence. Results: We developed a structured strategy with innovative applications of existing bioinformatics methods for supervised analyses including: 1) the combination of two statistical (t- and Anderson-Darling) test results to detect miRNAs with significant fold change or general distributional differences in class comparison, which could reveal hidden differential biological processes worth to be considered for building predictive tools; and 2) a bootstrap selection procedure together with machine learning techniques in class prediction to guarantee the transferability of results and explore the interconnections among the selected miRNAs, which is important for highlighting their inherent biological dependences. The strategy was applied to develop a classifier for discriminating between hemolyzed and non hemolyzed plasma samples, defined according to a recently published hemolysis score. We identified five miRNAs with increased expression in hemolyzed plasma samples (miR-486-5p, miR-92a, miR-451, miR-16, and miR-22). Conclusions: We identified four miRNAs previously reported in the literature as hemolysis related together with a new one (miR-22) which needs further investigations. Our findings confirm the validity of the proposed strategy and, in parallel, the hemolysis score capability to be used as pre-analytic hemolysis detector. R codes for implementing the approaches are provided.

Biography :

Elena Landoni has completed her PhD from University of Milan, Italy. She is working as a Biostatistician at the Fondazione IRCCS Istituto Nazionale dei Tumori in Milan. Her research involves the application of machine learning methods for the analysis of high-dimensional ‘omics’ data. In particular, she is focused on the discovery and development of cancer molecular biomarkers, with implementation of feature selection algorithms together with the use of original and simple graphical representations of the results. Another area of her interests is nonparametric statistics, applied in particular to the fields of molecular biology and personalized medicine.

Email: Elena.Landoni@istitutotumori.mi.it

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