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1.
Adv Data Anal Classif ; : 1-25, 2022 Sep 28.
Article in English | MEDLINE | ID: mdl-36188101

ABSTRACT

The number of daily credit card transactions is inexorably growing: the e-commerce market expansion and the recent constraints for the Covid-19 pandemic have significantly increased the use of electronic payments. The ability to precisely detect fraudulent transactions is increasingly important, and machine learning models are now a key component of the detection process. Standard machine learning techniques are widely employed, but inadequate for the evolving nature of customers behavior entailing continuous changes in the underlying data distribution. his problem is often tackled by discarding past knowledge, despite its potential relevance in the case of recurrent concepts. Appropriate exploitation of historical knowledge is necessary: we propose a learning strategy that relies on diversity-based ensemble learning and allows to preserve past concepts and reuse them for a faster adaptation to changes. In our experiments, we adopt several state-of-the-art diversity measures and we perform comparisons with various other learning approaches. We assess the effectiveness of our proposed learning strategy on extracts of two real datasets from two European countries, containing more than 30 M and 50 M transactions, provided by our industrial partner, Worldline, a leading company in the field.

2.
Hum Mutat ; 41(2): 512-524, 2020 02.
Article in English | MEDLINE | ID: mdl-31696992

ABSTRACT

Primary microcephaly (PM) is characterized by a small head since birth and is vastly heterogeneous both genetically and phenotypically. While most cases are monogenic, genetic interactions between Aspm and Wdr62 have recently been described in a mouse model of PM. Here, we used two complementary, holistic in vivo approaches: high throughput DNA sequencing of multiple PM genes in human patients with PM, and genome-edited zebrafish modeling for the digenic inheritance of PM. Exomes of patients with PM showed a significant burden of variants in 75 PM genes, that persisted after removing monogenic causes of PM (e.g., biallelic pathogenic variants in CEP152). This observation was replicated in an independent cohort of patients with PM, where a PM gene panel showed in addition that the burden was carried by six centrosomal genes. Allelic frequencies were consistent with digenic inheritance. In zebrafish, non-centrosomal gene casc5 -/- produced a severe PM phenotype, that was not modified by centrosomal genes aspm or wdr62 invalidation. A digenic, quadriallelic PM phenotype was produced by aspm and wdr62. Our observations provide strong evidence for digenic inheritance of human PM, involving centrosomal genes. Absence of genetic interaction between casc5 and aspm or wdr62 further delineates centrosomal and non-centrosomal pathways in PM.


Subject(s)
Centrosome/metabolism , Genetic Association Studies , Genetic Predisposition to Disease , Inheritance Patterns , Microcephaly/diagnosis , Microcephaly/genetics , Animals , Databases, Genetic , Genetic Association Studies/methods , Humans , Mutation , Open Reading Frames , Phenotype , Signal Transduction , Exome Sequencing , Zebrafish
3.
Med Sci (Paris) ; 29(5): 529-36, 2013 May.
Article in French | MEDLINE | ID: mdl-23732103

ABSTRACT

The musculoskeletal system (MSS) is essential to allow us performing every-day tasks, being able to have a professional life or developing social interactions with our entourage. MSS pathologies have a significant impact on our daily life. It is therefore not surprising to find MSS-related health problems at the top of global statistics on professional absenteeism or societal health costs. The MSS is also involved in central nervous conditions, such as cerebral palsy (CP). Such conditions show complex etiology that complicates the interpretation of the observable clinical signs and the establishment of a wide consensus on the best practices to adopt for clinical monitoring and patient follow-up. These elements justify the organization of fundamental and applied research projects aiming to develop new methods to help clinicians to cope with the complexity of some MSS disorders. The ICT4Rehab project (www.ict4rehab.org) developed an integrated platform providing tools that enable easier management and visualization of clinical information related to the MSS of CP patients. This platform is opened to every interested clinical centre.


Subject(s)
Cerebral Palsy/rehabilitation , Health Records, Personal , Humans
4.
Sensors (Basel) ; 8(8): 4821-4850, 2008 Aug 11.
Article in English | MEDLINE | ID: mdl-27873788

ABSTRACT

The Principal Component Analysis (PCA) is a data dimensionality reduction technique well-suited for processing data from sensor networks. It can be applied to tasks like compression, event detection, and event recognition. This technique is based on a linear transform where the sensor measurements are projected on a set of principal components. When sensor measurements are correlated, a small set of principal components can explain most of the measurements variability. This allows to significantly decrease the amount of radio communication and of energy consumption. In this paper, we show that the power iteration method can be distributed in a sensor network in order to compute an approximation of the principal components. The proposed implementation relies on an aggregation service, which has recently been shown to provide a suitable framework for distributing the computation of a linear transform within a sensor network. We also extend this previous work by providing a detailed analysis of the computational, memory, and communication costs involved. A compression experiment involving real data validates the algorithm and illustrates the tradeoffs between accuracy and communication costs.

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