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Ruberto, S.

Publications and source records attributed to Ruberto, S..

2 recordsLinked to original sources

Embedding covariate adjustments in tree-based automated machine learning for biomedical big data analyses

BackgroundA typical task in bioinformatics consists of identifying which features are associated with a target outcome of interest and building a predictive model. Automated machine learning (AutoML) systems such as the Tree-based Pipeline Optimization Tool (TPOT) constitute an appealing approach to this end. However, in biomedical data, there are often baseline characteristics of the subjects in a study or batch effects that need to be adjusted for in order to better isolate the effects of the features of interest on the target. Thus, the ability to perform covariate adjustments becomes particularly important for applications of AutoML to biomedical big data analysis. ResultsWe present an approach to adjust for covariates affecting features and/or target in TPOT. Our approach is based on regressing out the covariates in a manner that avoids leakage during the cross-validation training procedure. We then describe applications of this approach to toxicogenomics and schizophrenia gene expression data sets. The TPOT extensions discussed in this work are available at https://github.com/EpistasisLab/tpot/tree/v0.11.1-resAdj. ConclusionsIn this work, we address an important need in the context of AutoML, which is particularly crucial for applications to bioinformatics and medical informatics, namely covariate adjustments. To this end we present a substantial extension of TPOT, a genetic programming based AutoML approach. We show the utility of this extension by applications to large toxicogenomics and differential gene expression data. The method is generally applicable in many other scenarios from the biomedical field.

bioinformatics↗

Evaluation of the possible association of Body Mass Index and four metabolic gene polymorphisms with longevity in an Italian cohort: a role for APOE, eNOS, and FTO gene polymorphisms.

Backgroundlongevity is considered the result of interactions between environmental and genetic factors.\n\nAimwe investigated the possible association of body mass index and the frequencies of APOE, ACE, eNOS, and FTO gene polymorphisms with longevity.\n\nSubjects and Method1,100 healthy volunteers aged 10-100 were recruited. We genotyped subjects for APOE, ACE, eNOS, and FTO gene polymorphisms. Data about height and weight were also collected. The sample was split in four age groups: 1-24, 25-49, 50-85 and 86-100.\n\nResultssignificant differences were found in BMI values between age groups, with exception of 1-24 with respect to 86-100. A significant decrease of the APO E4, eNOS 393 and FTO A and allele frequencies was observed in the 86-100 age group with respect to younger groups. For ACE gene, no significant differences were found in the allele frequencies between groups. A similar trend was also observed subdividing the sample in two main age groups: 1-85 and 86-100.\n\nConclusionthis study provides evidences for a role of APOE, eNOS, and FTO gene polymorphisms in longevity. It has been estimated that the number of centenarians worldwide will double each decade until 2100, making population data about gene polymorphisms relevant for further studies about longevity.

genetics↗