Egalisation autodidacte d'un signal modulé en fréquence

Nous traitons du problème de l'égalisation autodidacte d'un canal linéaire dans le cas d'un signal modulé en fréquence ou en phase. Le problème de l'annulation d'interférences canal adjacent est aussi abordé. Dans cet article, nous proposons une structure récursive, basée sur le critère de Godard[1], et qui utilise la stratégie d'égalisation par prédiction et rétroprédiction proposée par Macchi et al [2]. La nouvelle structure est comparée au CMA classique, et les résultats obtenus montrent la supériorité de l'approche récursive par rapport à l'approche transversale dans l'égalisation de canaux à trajets multiples. Enfin, la structure récursive présente des performances équivalentes au CMA pour l'annulation d'interférences

Anisotropy of electrical conductivity of the Excavation Damaged Zone in the Mont Terri Underground Rock Laboratory

International audienceElectrical resistivity measurements were performed to characterize the anisotropy of electrical resistivity of the excavation damaged zone (EDZ) at the end-face of a gallery in the Opalinus clay of the Mont Terri Underground Rock Laboratory (URL). The data were acquired with a combination of square arrays in 18 zones on the gallery's face and in two series of four boreholes perpendicular to the face. Each data set is independently inverted using simulated annealing to recover the resistivity tensor. Both the stability and the non-uniqueness of the inverse problem are discussed with synthetic examples. The inversion of the data shows that the face is split in two domains separated by a tectonic fracture, with different resistivity values but with a common orientation. The direction of the maximum resistivity is found perpendicular to the bedding plane, and the direction of minimum resistivity is contained in the face's plane. These results show that the geo-electrical structure of the EDZ is controlled by a combination of effects due to tectonics, stratigraphy, and recent fracturing produced by the excavation of the gallery

UNE PLATEFORME RADIO LOGICIELLE OUVERTE POUR LES SYSTÈMES 3G+

This paper describes a software-radio architecture developed for providing real-time wide-band radio communication capabilities in a form attractive for advanced 3G systems research. It is currently being used to implement signaling methods and protocols similar, but not limited to, evolving 3G radio standards (e.g. umts, cdma2000). An overview of the hardware system is provided along with example software implementations on both high-perfo-mance DSP systems and conventional microprocessor

Quantum correlations and distinguishability of quantum states

A survey of various concepts in quantum information is given, with a main emphasis on the distinguishability of quantum states and quantum correlations. Covered topics include generalized and least square measurements, state discrimination, quantum relative entropies, the Bures distance on the set of quantum states, the quantum Fisher information, the quantum Chernoff bound, bipartite entanglement, the quantum discord, and geometrical measures of quantum correlations. The article is intended both for physicists interested not only by collections of results but also by the mathematical methods justifying them, and for mathematicians looking for an up-to-date introductory course on these subjects, which are mainly developed in the physics literature.Comment: Review article, 103 pages, to appear in J. Math. Phys. 55 (special issue: non-equilibrium statistical mechanics, 2014

Architectures for Cognitive Radio Testbeds and Demonstrators – An Overview

Wireless communication standards are developed at an ever-increasing rate of pace, and significant amounts of effort is put into research for new communication methods and concepts. On the physical layer, such topics include MIMO, cooperative communication, and error control coding, whereas research on the medium access layer includes link control, network topology, and cognitive radio. At the same time, implementations are moving from traditional fixed hardware architectures towards software, allowing more efficient development. Today, field-programmable gate arrays (FPGAs) and regular desktop computers are fast enough to handle complete baseband processing chains, and there are several platforms, both open-source and commercial, providing such solutions. The aims of this paper is to give an overview of five of the available platforms and their characteristics, and compare the features and performance measures of the different systems

Evaluation of polygenic risk scores for breast and ovarian cancer risk prediction in BRCA1 and BRCA2 mutation carriers

Background: Genome-wide association studies (GWAS) have identified 94 common single-nucleotide polymorphisms (SNPs) associated with breast cancer (BC) risk and 18 associated with ovarian cancer (OC) risk. Several of these are also associated with risk of BC or OC for women who carry a pathogenic mutation in the high-risk BC and OC genes BRCA1 or BRCA2. The combined effects of these variants on BC or OC risk for BRCA1 and BRCA2 mutation carriers have not yet been assessed while their clinical management could benefit from improved personalized risk estimates. Methods: We constructed polygenic risk scores (PRS) using BC and OC susceptibility SNPs identified through population-based GWAS: for BC (overall, estrogen receptor [ER]-positive, and ER-negative) and for OC. Using data from 15 252 female BRCA1 and 8211 BRCA2 carriers, the association of each PRS with BC or OC risk was evaluated using a weighted cohort approach, with time to diagnosis as the outcome and estimation of the hazard ratios (HRs) per standard deviation increase in the PRS. Results: The PRS for ER-negative BC displayed the strongest association with BC risk in BRCA1 carriers (HR = 1.27, 95% confidence interval [CI] = 1.23 to 1.31, P = 8.2 x 10(53)). In BRCA2 carriers, the strongest association with BC risk was seen for the overall BC PRS (HR = 1.22, 95% CI = 1.17 to 1.28, P = 7.2 x 10(-20)). The OC PRS was strongly associated with OC risk for both BRCA1 and BRCA2 carriers. These translate to differences in absolute risks (more than 10% in each case) between the top and bottom deciles of the PRS distribution; for example, the OC risk was 6% by age 80 years for BRCA2 carriers at the 10th percentile of the OC PRS compared with 19% risk for those at the 90th percentile of PRS. Conclusions: BC and OC PRS are predictive of cancer risk in BRCA1 and BRCA2 carriers. Incorporation of the PRS into risk prediction models has promise to better inform decisions on cancer risk management

BRCA2 polymorphic stop codon K3326X and the risk of breast, prostate, and ovarian cancers

Background: The K3326X variant in BRCA2 (BRCA2*c.9976A>T; p.Lys3326*; rs11571833) has been found to be associated with small increased risks of breast cancer. However, it is not clear to what extent linkage disequilibrium with fully pathogenic mutations might account for this association. There is scant information about the effect of K3326X in other hormone-related cancers. Methods: Using weighted logistic regression, we analyzed data from the large iCOGS study including 76 637 cancer case patients and 83 796 control patients to estimate odds ratios (ORw) and 95% confidence intervals (CIs) for K3326X variant carriers in relation to breast, ovarian, and prostate cancer risks, with weights defined as probability of not having a pathogenic BRCA2 variant. Using Cox proportional hazards modeling, we also examined the associations of K3326X with breast and ovarian cancer risks among 7183 BRCA1 variant carriers. All statistical tests were two-sided. Results: The K3326X variant was associated with breast (ORw = 1.28, 95% CI = 1.17 to 1.40, P = 5.9x10- 6) and invasive ovarian cancer (ORw = 1.26, 95% CI = 1.10 to 1.43, P = 3.8x10-3). These associations were stronger for serous ovarian cancer and for estrogen receptor–negative breast cancer (ORw = 1.46, 95% CI = 1.2 to 1.70, P = 3.4x10-5 and ORw = 1.50, 95% CI = 1.28 to 1.76, P = 4.1x10-5, respectively). For BRCA1 mutation carriers, there was a statistically significant inverse association of the K3326X variant with risk of ovarian cancer (HR = 0.43, 95% CI = 0.22 to 0.84, P = .013) but no association with breast cancer. No association with prostate cancer was observed. Conclusions: Our study provides evidence that the K3326X variant is associated with risk of developing breast and ovarian cancers independent of other pathogenic variants in BRCA2. Further studies are needed to determine the biological mechanism of action responsible for these associations

Lifelong testicular differentiation in Pleurodeles waltl (Amphibia, Caudata)

This is an Open Access article distributed under the terms of the Creative Commons Attribution Licens

Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women

Background: Most BRCA1 or BRCA2 mutation carriers have inherited a single (heterozygous) mutation. Transheterozygotes (TH) who have inherited deleterious mutations in both BRCA1 and BRCA2 are rare, and the consequences of transheterozygosity are poorly understood. Methods: From 32,295 female BRCA1/2 mutation carriers, we identified 93 TH (0.3 %). "Cases" were defined as TH, and "controls" were single mutations at BRCA1 (SH1) or BRCA2 (SH2). Matched SH1 "controls" carried a BRCA1 mutation found in the TH "case". Matched SH2 "controls" carried a BRCA2 mutation found in the TH "case". After matching the TH carriers with SH1 or SH2, 91 TH were matched to 9316 SH1, and 89 TH were matched to 3370 SH2. Results: The majority of TH (45.2 %) involved the three common Jewish mutations. TH were more likely than SH1 and SH2 women to have been ever diagnosed with breast cancer (BC; p = 0.002). TH were more likely to be diagnosed with ovarian cancer (OC) than SH2 (p = 0.017), but not SH1. Age at BC diagnosis was the same in TH vs. SH1 (p = 0.231), but was on average 4.5 years younger in TH than in SH2 (p < 0.001). BC in TH was more likely to be estrogen receptor (ER) positive (p = 0.010) or progesterone receptor (PR) positive (p = 0.013) than in SH1, but less likely to be ER positive (p < 0.001) or PR positive (p = 0.012) than SH2. Among 15 tumors from TH patients, there was no clear pattern of loss of heterozygosity (LOH) for BRCA1 or BRCA2 in either BC or OC. Conclusions: Our observations suggest that clinical TH phenotypes resemble SH1. However, TH breast tumor marker characteristics are phenotypically intermediate to SH1 and SH2