Kaldi-web: An installation-free, on-device speech recognition system

International audienceSpeech provides an intuitive interface to communicate with machines. Today, developers willing to implement such an interface must either rely on third-party proprietary software or become experts in speech recognition. Conversely, researchers in speech recognition wishing to demonstrate their results need to be familiar with technologies that are not relevant to their research (e.g., graphical user interface libraries). In this demo, we introduce Kaldi-web: an open-source, cross-platform tool which bridges this gap by providing a user interface built around the online decoder of the Kaldi toolkit. Additionally, because we compile Kaldi to Web Assembly, speech recognition is performed directly in web browsers. This addresses privacy issues as no data is transmitted to the network for speech recognition

Création de livres numériques pour enfants présentant des troubles du langage

Démonstration de la création de livres numériques à la conférence IHM 2010 au Luxembourg du 20 au 23 septembre 2010.National audienceThis paper describes a digital book making software, using a speaking and coding head.Cet article décrit un logiciel de création de livres numé- riques illustrés, associant une tête parlante et codeuse en LPC (Langage Parlé Complété). Ces livres numériques, destinés à des enfants présentants des troubles du langa- ge, ont pour objectif d'aider à améliorer la maîtrise de la langue française, dans ses modalités orale et écrite

Genetic Admixture and Flavor Preferences: Androstenone Sensitivity in Malagasy Populations

The genetic basis of androstenone anosmia has been well-studied due to androstenone’s putative role as a human sex pheromone and its presence in pork meat. Polymorphisms have been identified on the olfactory receptor gene OR7D4, which significantly affect perception of androstenone pleasantness and intensity in several western populations. This study aims to investigate androstenone sensitivity and the influence of OR7D4 polymorphisms in non-western populations. Androstenone perception was tested in 132 individuals from Madagascar using a double 3-Alternative Choice test with two concentrations of androstenone (0.17 μg/ml and 1.7 μg/ml). We found that Malagasy populations described this molecule in a similar way to European populations, and 21% of the sample was not able to smell androstenone. In contrast to previous studies, there was no significant evidence of the influence of rs61729907: C\u3eT (R88W) and rs5020278: C\u3eT polymorphisms (T133M) on androstenone sensitivity in Malagasy populations. We found, however, a significant effect of the polymorphism rs61732668 (P79L), and a significant difference in androstenone perception between populations in different locations across Madagascar. This study indicates the existence of population specific factors to androstenone sensitivity, suggesting that population history has a role in shaping an individual’s smell and flavor preferences, and food preferences in general

Histoire évolutive de la maladie carieuse : exemple des populations inuites

La maladie carieuse est une pathologie considérée comme le troisième fléau mondial par l’Organisation Mondiale de la Santé, puisqu’elle touche plus de 99 % des adultes. Historiquement, en Europe, la prévalence carieuse augmente progressivement depuis le Néolithique jusqu’à atteindre un pic au XXe siècle et ne commence à diminuer que depuis les 25 dernières années. Cependant, cette maladie n’a pas connu la même histoire évolutive dans toutes les populations humaines. Dans le cadre d’une thèse,..

Histoire démographique des ancêtres de la population malgache actuelle à partir des données génétiques

Bien que situé à 400 km de l’Afrique, les habitants de Mada­gascar partagent des caractéristiques linguistiques, culturelles et génétiques avec des populations d’Indonésie et de la côte Est d’Afrique. Il a été montré que la population malgache est issue d’un mélange entre des populations bantu et austronésienne pendant le dernier millenium. Néanmoins, l’histoire du peuplement de l’île par les ancêtres de la population malgache actuelle reste encore incomplet et confus. Ici, nous cherchons à e..

New evidence of a mitochondrial genetic background paradox: Impact of the J haplogroup on the A3243G mutation

International audienceBackground: The A3243G mutation in the tRNALeu gene (UUR), is one of the most common pathogenic mitochondrial DNA (mtDNA) mutations in France, and is associated with highly variable and heterogeneous disease phenotypes. To define the relationships between the A3243G mutation and mtDNA backgrounds, we determined the haplogroup affiliation of 142 unrelated French patients – diagnosed as carriers of the A3243G mutation – by control-region sequencing and RFLP survey of their mtDNAs. Results: The analysis revealed 111 different haplotypes encompassing all European haplogroups, indicating that the 3243 site might be a mutational hot spot. However, contrary to previous findings, we observed a statistically significant underepresentation of the A3243G mutation on haplogroup J in patients (p = 0.01, OR = 0.26, C.I. 95%: 0.08–0.83), suggesting that might be due to a strong negative selection at the embryo or germ line stages. Conclusion: Thus, our study supports the existence of mutational hotspot on mtDNA and a "haplogroup J paradox," a haplogroup that may increase the expression of mtDNA pathogenic mutations, but also be beneficial in certain environmental contexts

Mutation Rate Switch inside Eurasian Mitochondrial Haplogroups: Impact of Selection and Consequences for Dating Settlement in Europe

R-lineage mitochondrial DNA represents over 90% of the European population and is significantly present all around the planet (North Africa, Asia, Oceania, and America). This lineage played a major role in migration “out of Africa” and colonization in Europe. In order to determine an accurate dating of the R lineage and its sublineages, we analyzed 1173 individuals and complete mtDNA sequences from Mitomap. This analysis revealed a new coalescence age for R at 54.500 years, as well as several limitations of standard dating methods, likely to lead to false interpretations. These findings highlight the association of a striking under-accumulation of synonymous mutations, an over-accumulation of non-synonymous mutations, and the phenotypic effect on haplogroup J. Consequently, haplogroup J is apparently not a Neolithic group but an older haplogroup (Paleolithic) that was subjected to an underestimated selective force. These findings also indicated an under-accumulation of synonymous and non-synonymous mutations localized on coding and non-coding (HVS1) sequences for haplogroup R0, which contains the major haplogroups H and V. These new dates are likely to impact the present colonization model for Europe and confirm the late glacial resettlement scenario

OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background

<p>Abstract</p> <p>Background</p> <p>Leber's hereditary optic neuropathy (LHON) and autosomal dominant optic atrophy (ADOA) are the most frequent forms of hereditary optic neuropathies. LHON is associated with mitochondrial DNA (mtDNA) mutations whereas ADOA is mainly due to mutations in the OPA1 gene that encodes a mitochondrial protein involved in the mitochondrial inner membrane remodeling. A striking influence of mtDNA haplogroup J on LHON expression has been demonstrated and it has been recently suggested that this haplogroup could also influence ADOA expression. In this study, we have tested the influence of mtDNA backgrounds on OPA1 mutations.</p> <p>Methods</p> <p>To define the relationships between OPA1 mutations and mtDNA backgrounds, we determined the haplogroup affiliation of 41 French patients affected by OPA1-related ADOA by control-region sequencing and RFLP survey of their mtDNAs.</p> <p>Results</p> <p>The comparison between patient and reference populations did not revealed any significant difference.</p> <p>Conclusion</p> <p>Our results argue against a strong influence of mtDNA background on ADOA expression. These data allow to conclude that OPA1 could be considered as a "severe mutation", directly responsible of the optic atrophy, whereas OPA1-negative ADOA and LHON mutations need an external factor(s) to express the pathology (i.e. synergistic interaction with mitochondrial background).</p

Smell and taste changes are early indicators of the COVID-19 pandemic and political decision effectiveness

In response to the COVID-19 pandemic, many governments have taken drastic measures to avoid an overflow of intensive care units. Accurate metrics of disease spread are critical for the reopening strategies. Here, we show that self-reports of smell/taste changes are more closely associated with hospital overload and are earlier markers of the spread of infection of SARS-CoV-2 than current governmental indicators. We also report a decrease in self-reports of new onset smell/taste changes as early as 5 days after lockdown enforcement. Cross-country comparisons demonstrate that countries that adopted the most stringent lockdown measures had faster declines in new reports of smell/taste changes following lockdown than a country that adopted less stringent lockdown measures. We propose that an increase in the incidence of sudden smell and taste change in the general population may be used as an indicator of COVID-19 spread in the population

Contribution de l’anthropologie sensorielle à l’étude du COVID-19

En réponse à la pandémie COVID-19, de nombreux gouvernements ont pris des mesures sans précédent pour éviter un engorgement des unités de réanimation. En raison du lourd impact sociétal et économique de ces initiatives, des indicateurs épidémiologiques précis de la propagation de la maladie sont essentiels aux autorités de santé publique. Dans le même temps, la perturbation des perceptions des odeurs et du goût ont été identifiés comme l’un des symptômes les plus spécifiques de la maladie COV..