Thesis, COLLÉGIALITÉ
Zaccone, Gaetano
Promotor(s) : Dubourdeau, Marc ; Widart, Joëlle ; Poulet, Christophe
Date of defense : 1-Jul-2024 • Permalink : http://hdl.handle.net/2268.2/20567
Details
Title : | Thesis, COLLÉGIALITÉ |
Translated title : | [fr] Développement d'un pipeline d'anlyse pour réaliser des comparaisons multiples sur les données lipidomiques de patients SAIDs |
Author : | Zaccone, Gaetano |
Date of defense : | 1-Jul-2024 |
Advisor(s) : | Dubourdeau, Marc
Widart, Joëlle Poulet, Christophe |
Committee's member(s) : | Lavergne, Arnaud
Blomme, Arnaud Papadaki, Maria |
Language : | English |
Number of pages : | 46 |
Keywords : | [en] SAIDs, autoinflammation, data analysis, computational biology |
Discipline(s) : | Human health sciences > Laboratory medicine & medical technology |
Funders : | Ambiotis (CRO) |
Research unit : | Ambiotis (CRO) |
Target public : | Professionals of domain |
Institution(s) : | Université de Liège, Liège, Belgique |
Degree: | Master en sciences biomédicales, à finalité spécialisée en biomédical data management |
Faculty: | Master thesis of the Faculté de Médecine |
Abstract
[en] Systemic AutoInflammatory Disorders or SAIDs constitute rare diseases where the innate immune response is dysregulated. Though there are genes mutations that are associated with monogenic SAIDs, polygenic ones have higher incidence and are more difficult to diagnose. Ambiotis, a CRO based in Toulouse (FR) and with an expertise in the resolution of inflammation hypothesize SAIDs patients have a dysregulated resolution of inflammation. In the context of the Immunome consortium for AutoInflammatory Disorders or ImmunAID, a European Union funded project, a cohort of SAIDs patients was created throughout Europe to collect biological sample. These sample would be analysed by multiple omics techniques to acquire the immunome of SAIDs as a group and as the different diseases. Ambiotis, part of the ImmunAID consortium, quantified Specialized Pro-resolution Mediators (SPM) using UHPLC-MS technique. This master’s thesis goal was to design a pipeline and R library to process the lipidomic data, run multiple pairwise comparison and display results in different graphs format. Our pipeline was able to identify protectin D1 having higher concentration in some SAIDs when compared to negative controls.
These results were obtained on the quantified data available; the next step will be to use the entire data set. In the end, we managed to build a pipeline that correct the batch effect, normalize the data and run multiple pairwise comparisons.
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