244 research outputs found

    The FruitShell French synthesis system at the Blizzard 2023 Challenge

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    This paper presents a French text-to-speech synthesis system for the Blizzard Challenge 2023. The challenge consists of two tasks: generating high-quality speech from female speakers and generating speech that closely resembles specific individuals. Regarding the competition data, we conducted a screening process to remove missing or erroneous text data. We organized all symbols except for phonemes and eliminated symbols that had no pronunciation or zero duration. Additionally, we added word boundary and start/end symbols to the text, which we have found to improve speech quality based on our previous experience. For the Spoke task, we performed data augmentation according to the competition rules. We used an open-source G2P model to transcribe the French texts into phonemes. As the G2P model uses the International Phonetic Alphabet (IPA), we applied the same transcription process to the provided competition data for standardization. However, due to compiler limitations in recognizing special symbols from the IPA chart, we followed the rules to convert all phonemes into the phonetic scheme used in the competition data. Finally, we resampled all competition audio to a uniform sampling rate of 16 kHz. We employed a VITS-based acoustic model with the hifigan vocoder. For the Spoke task, we trained a multi-speaker model and incorporated speaker information into the duration predictor, vocoder, and flow layers of the model. The evaluation results of our system showed a quality MOS score of 3.6 for the Hub task and 3.4 for the Spoke task, placing our system at an average level among all participating teams

    Emergence of central recirculation zone in a V-shaped premixed swirling flame

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    This paper presents an experimental study on the emergence of the central recirculation zone (CRZ) in a V-shaped premixed swirling flame, using simultaneous measurement of particle image velocimetry (PIV) and CH* chemiluminescence. The results show that either increasing the Reynolds number (Re) or decreasing the equivalence ratio ({\phi}) would facilitate the emergence of CRZ, and the inner shear layer (ISL) plays an essential role in governing the characteristics of CRZ. Further analysis demonstrates that the CRZ emergence can be promoted by higher ISL intensity but suppressed by enhanced viscous diffusion owing to higher flame temperature. As such, the CRZ formation can be interpreted as the outcome of a competition between the ISL intensity, i.e., circulation, and the vorticity consumption due to viscous diffusion. This competition physically corresponds to a special Reynolds number, Re_s, defined as the ratio between the ISL circulation ({\Gamma}) and the ISL effective viscosity ({\nu}_s), with a simplified heat loss model proposed for the temperature and viscosity estimations of the ISL. The outputting {\Gamma}-{\nu}_s plot yields a single boundary line separating the cases with and without CRZ, which points to a common critical Re_s of about 637, justifying the generality of the present criterion for lean-premixed V-shaped swirling flames of various operating conditions. Unlike most previous works which study the CRZ of a swirling flame from the point of vortex breakdown, the present work reveals the importance of enhanced viscous diffusion, caused by flame heating, in suppressing the CRZ emergence

    Exploring Effective Mask Sampling Modeling for Neural Image Compression

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    Image compression aims to reduce the information redundancy in images. Most existing neural image compression methods rely on side information from hyperprior or context models to eliminate spatial redundancy, but rarely address the channel redundancy. Inspired by the mask sampling modeling in recent self-supervised learning methods for natural language processing and high-level vision, we propose a novel pretraining strategy for neural image compression. Specifically, Cube Mask Sampling Module (CMSM) is proposed to apply both spatial and channel mask sampling modeling to image compression in the pre-training stage. Moreover, to further reduce channel redundancy, we propose the Learnable Channel Mask Module (LCMM) and the Learnable Channel Completion Module (LCCM). Our plug-and-play CMSM, LCMM, LCCM modules can apply to both CNN-based and Transformer-based architectures, significantly reduce the computational cost, and improve the quality of images. Experiments on the public Kodak and Tecnick datasets demonstrate that our method achieves competitive performance with lower computational complexity compared to state-of-the-art image compression methods.Comment: 10 page

    S3IM: Stochastic Structural SIMilarity and Its Unreasonable Effectiveness for Neural Fields

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    Recently, Neural Radiance Field (NeRF) has shown great success in rendering novel-view images of a given scene by learning an implicit representation with only posed RGB images. NeRF and relevant neural field methods (e.g., neural surface representation) typically optimize a point-wise loss and make point-wise predictions, where one data point corresponds to one pixel. Unfortunately, this line of research failed to use the collective supervision of distant pixels, although it is known that pixels in an image or scene can provide rich structural information. To the best of our knowledge, we are the first to design a nonlocal multiplex training paradigm for NeRF and relevant neural field methods via a novel Stochastic Structural SIMilarity (S3IM) loss that processes multiple data points as a whole set instead of process multiple inputs independently. Our extensive experiments demonstrate the unreasonable effectiveness of S3IM in improving NeRF and neural surface representation for nearly free. The improvements of quality metrics can be particularly significant for those relatively difficult tasks: e.g., the test MSE loss unexpectedly drops by more than 90% for TensoRF and DVGO over eight novel view synthesis tasks; a 198% F-score gain and a 64% Chamfer L1L_{1} distance reduction for NeuS over eight surface reconstruction tasks. Moreover, S3IM is consistently robust even with sparse inputs, corrupted images, and dynamic scenes.Comment: ICCV 2023 main conference. Code: https://github.com/Madaoer/S3IM. 14 pages, 5 figures, 17 table

    Probing Complex-energy Topology via Non-Hermitian Absorption Spectroscopy in a Trapped Ion Simulator

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    Non-Hermitian systems generically have complex energies, which may host topological structures, such as links or knots. While there has been great progress in experimentally engineering non-Hermitian models in quantum simulators, it remains a significant challenge to experimentally probe complex energies in these systems, thereby making it difficult to directly diagnose complex-energy topology. Here, we experimentally realize a two-band non-Hermitian model with a single trapped ion whose complex eigenenergies exhibit the unlink, unknot or Hopf link topological structures. Based on non-Hermitian absorption spectroscopy, we couple one system level to an auxiliary level through a laser beam and then experimentally measure the population of the ion on the auxiliary level after a long period of time. Complex eigenenergies are then extracted, illustrating the unlink, unknot or Hopf link topological structure. Our work demonstrates that complex energies can be experimentally measured in quantum simulators via non-Hermitian absorption spectroscopy, thereby opening the door for exploring various complex-energy properties in non-Hermitian quantum systems, such as trapped ions, cold atoms, superconducting circuits or solid-state spin systems.Comment: 12 pages, 8 figure

    Cardiotoxicity of lung cancer-related immunotherapy versus chemotherapy: a systematic review and network meta-analysis of randomized controlled trials

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    BackgroundPrevious clinical randomized controlled trials (RCTs) have demonstrated that immune checkpoint inhibitors (ICIs) cause various toxicities during cancer treatment, but the effects of different inhibitors in combination with chemotherapy for cardiotoxicity remain controversial. The aim of the present study was to assess cardiotoxicity caused by programmed cell death protein 1 (PD-1), programmed cell death-Ligand 1 (PD-L1), and cytotoxic T lymphocyte associate protein-4 (CTLA-4) in combination with chemotherapy to treat lung cancer.MethodsThe following ICIs were included in the present study: durvalumab, avelumab, ipilimumab, atezolizumab, pembrolizumab, cemiplimab, and nivolumab. The relevant information was extracted using a predefined data extraction table, and the risk of bias was assessed in randomized controlled trials using the Cochrane Bias Risk tool. The main outcomes were hypertension, heart failure, pericardial effusion, and other adverse cardiac events. The random effects model was used to conduct a paired meta-analysis, and a random effects network meta-analysis was then performed within a Bayesian framework.ResultsIn total, 17 RCTs were included in the present study. There were 11,063 individuals in the experimental and control groups, with an average age greater than 60 years. Based on the evaluation of all drug classes in RCTs, CTLA-4+chemotherapy (RR, -0.69 [95% CI, 2.91-1.52] and PD-L1 (RR, -0.21 [95% CI, -1.03-0.60]) were less cardiotoxic than the control arm, which indicated they were safer options for adverse cardiac events. PD-L1 alone was less cardiotoxic than PD-1 alone (RR, -0.57 [95% CI, -1.96-0.82]). Further, the dual immunotarget inhibitor, PD-1+CTLA-4, had the lowest SUCRA value and had the highest cardiotoxicity (SUCRA=9).ConclusionWhen classified according to drug type, CTLA-4+chemotherapy is associated with fewer cardiac adverse events compared to other treatments. Dual immunotarget inhibitors are more likely to have adverse cardiac reactions. Therefore, clinicians should consider this evidence when developing an ICI immunotherapy regimen for lung cancer.Systematic review registrationhttps://www.crd.york.ac.uk/prospero, identifier CRD42023360931

    Nano selenium-doped TiO2 nanotube arrays on orthopedic implants for suppressing osteosarcoma growth

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    Osteosarcoma, the most common primary malignant bone tumor, is characterized by malignant cells producing osteoid or immature bone tissue. Most osteosarcoma patients require reconstructive surgery to restore the functional and structural integrity of the injured bone. Metal orthopedic implants are commonly used to restore the limb integrity in postoperative patients. However, conventional metal implants with a bioinert surface cannot inhibit the growth of any remaining cancer cells, resulting in a higher risk of cancer recurrence. Herein, we fabricate a selenium-doped TiO2 nanotube array (Se-doped TNA) film to modify the surface of medical pure titanium substrate, and evaluate the anti-tumor effect and biocompatibility of Se-doped TNA film. Moreover, we further explore the anti-tumor potential mechanism of Se-doped TNA film by studying the behaviors of human osteosarcoma cells in vitro. We provide a new pathway for achieving the anti-tumor function of orthopedic implants while keeping the biocompatibility, aiming to suppress the recurrence of osteosarcoma

    The negative interplay between Aurora A/B and BRCA1/2 controls cancer cell growth and tumorigenesis via distinct regulation of cell cycle progression, cytokinesis, and tetraploidy

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    It is well known that the activation of Aurora A/B (Aur A/B) or inactivation of BRCA1/2 induces tumor formation. Others and we have reported that the mutual suppression between Aur A/B and BRCA1/2 may manipulate cancer cell growth and tumorigenesis, however, the interactive regulation and mechanism between these molecules are still elusive. In this study, by consecutive silencing of Aur A/B or/and BRCA1/2 with specific shRNAs, we showed that, in BRCA2-deficient pancreatic cancer cell line Capan-1 and in ovarian cancer cell line OVCA433, Aur A/B and BRCA1/2 inversely regulated the expression of each other likely through proteasome-mediated proteolysis but not through gene transcription. Aur A/B and BRCA1/2 conversely regulated cell cycle progression mainly through control of p53 and cyclin A. Moreover, the disruption of Aur A/B blocked abnormal cytokinesis and decreased cell multinuclearity and chromosome tetraploidy, whereas the deprivation of BRCA1/2 promoted the abnormal cytokinesis and enhanced the cell multinuclearity and tetraploidy. Furthermore, we showed by animal assays that the depletion of Aur A/B inhibited tumor growth of both cell lines, while the knockdown of BRCA1/2 promoted the tumor growth. However, the concurrent silencing of Aur A/B and BRCA1/2 diminished the effects of these molecules on the regulation of cell cycle, cytokinesis, and tetraploidy, leading to the burdened tumor sizes similar to those induced by scrambled shRNA-treated control cells. In summary, our study revealed that the negative interplay between Aur A/B and BRCA1/2 inversely controls the cell proliferation, cell cycle progression, cell multinuclearity, and tetraploidization to modulate tumorigenesis
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