154 research outputs found

    First attempt to build realistic driving scenes using video-to-video synthesis in OpenDS framework

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    Existing programmable simulators enable researchers to customize different driving scenarios to conduct in-lab automotive driver simulations. However, software-based simulators for cognitive research generate and maintain their scenes with the support of 3D engines, which may affect users' experiences to a certain degree since they are not sufficiently realistic. Now, a critical issue is the question of how to build scenes into real-world ones. In this paper, we introduce the first step in utilizing video-to-video synthesis, which is a deep learning approach, in OpenDS framework, which is an open-source driving simulator software, to present simulated scenes as realistically as possible. Off-line evaluations demonstrated promising results from our study, and our future work will focus on how to merge them appropriately to build a close-to-reality, real-time driving simulator

    miRAS: a data processing system for miRNA expression profiling study

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    <p>Abstract</p> <p>Background</p> <p>The study of microRNAs (miRNAs) is attracting great considerations. Recent studies revealed that miRNAs play as important regulators of gene expression and some even as cancer players or inhibitors. Many studies try to discover new miRNAs and reveal the miRNA expression profile in cancer using a SAGE-based total RNA clone method. However, the data processing of this method is labor-intensive with several different biological databases and more than ten data processing steps involved.</p> <p>Results</p> <p>With miRAS, miRNAs and possible miRNA candidates contained in the submitted sequencing data were obtained together with their expression profile. The functions of known and predicted miRNAs were then analyzed by miRNA target prediction followed by target gene annotations. Finally, to extract the biological significance of the miRNAs in the samples, further annotations of the known miRNA and target genes were performed by collecting the public expression datasets of miRNA and target genes in normal and cancer tissues.</p> <p>Conclusion</p> <p>We introduce a web-based analysis platform called miRNA Analysis System (miRAS), for processing and analyzing of the sequence data obtained from the total RNA clone method. The system was built on generalizing the study of a liver cancer cell line total RNA sequencing project. miRAS is freely available on the web.</p

    Face2Multi-modal: in-vehicle multi-modal predictors via facial expressions

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    Towards intelligent Human-Vehicle Interaction systems and innovative Human-Vehicle Interaction designs, in-vehicle drivers' physiological data has been explored as an essential data source. However, equipping multiple biosensors is considered the limited extent of user-friendliness and impractical during the driving procedure. The lack of a proper approach to access physiological data has hindered wider applications of advanced biosignal-driven designs in practice (e.g. monitoring systems and etc.). Hence, the demand for a user-friendly approach to measuring drivers' body statuses has become more intense. In this Work-In-Progress, we present Face2Multi-modal, an In-vehicle multi-modal Data Streams Predictors through facial expressions only. More specifically, we have explored the estimations of Heart Rate, Skin Conductance, and Vehicle Speed of the drivers. We believe Face2Multi-modal provides a user-friendly alternative to acquiring drivers' physiological status and vehicle status, which could serve as the building block for many current or future personalized Human-Vehicle Interaction designs. More details and updates about the project Face2Multi-modal is online at https://github.com/unnc-ucc/Face2Multimodal/

    Composite vertical structures and spatiotemporal characteristics of abnormal eddies in the Japan/East Sea: a synergistic investigation using satellite altimetry and Argo profiles

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    Mesoscale eddies are omnipresent and play an important role in regulating Earth’s climate and ocean circulation in the global ocean. Here using the combination of satellite altimetry products and Argo float profile data, two types of abnormal eddies are investigated: WCEs(warm cyclonic eddies) and CAEs(cold anticyclonic eddies) with different cores than conventional eddies in the Japan/East Sea. By applying a classification method based on the calculation of the heat content anomalies in the upper ocean, it was found that 10% of the eddies that captured the Argo float profiles exhibited obvious abnormal features. Subsequently, their spatiotemporal distributions and characteristics were analyzed statistically. Three-dimensional structures of abnormal eddies were obtained via the composite analysis method, showing that the warm/cold and light/dense core of the composite WCE/CAE is confined to the upper 100 m of the ocean with a maximum temperature anomaly of approximately +1.0(-1.1)°C. The composite WCE had a double-core salinity structure with a salty core above 50 m and an inferior fresh core. Meanwhile composite CAE had a fresh single-core with a maximum magnitude of -0.05 psu. Abnormal eddies are pervasive in the Japan/East sea, a revaluation of the role of these eddies in ocean circulation and climate systems, such as heat and salt transport, air and sea interaction, and variability in mixed layer depth, is of great importance

    Rapid detection of porcine circovirus type 4 via multienzyme isothermal rapid amplification

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    Porcine circovirus type 4 (PCV4) is a newly emerging pathogen that was first detected in 2019 and is associated with diverse clinical signs, including respiratory and gastrointestinal distress, dermatitis and various systemic inflammations. It was necessary to develop a sensitive and specific diagnostic method to detect PCV4 in clinical samples, so in this study, a multienzyme isothermal rapid amplification (MIRA) assay was developed for the rapid detection of PCV4 and evaluated for sensitivity, specificity and applicability. It was used to detect the conserved Cap gene of PCV4, operated at 41°C and completed in 20 min. With the screening of MIRA primer-probe combination, it could detect as low as 101 copies of PCV4 DNA per reaction and was highly specific, with no cross-reaction with other pathogens. Further assessment with clinical samples showed that the developed MIRA assay had good correlation with real-time polymerase chain reaction assay for the detection of PCV4. The developed MIRA assay will be a valuable tool for the detection of the novel PCV4 in clinical samples due to its high sensitivity and specificity, simplicity of operation and short testing time

    A multi-wavelength mid-IR laser based on BaGa4Se7 optical parametric oscillators

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    A multi-wavelength mid-IR laser consisting of 3.05 μm, 4.25 μm, and 5.47 μm BaGa4Se7(BGSe)optical parametric oscillators (OPOs) switched by DKDP electro-optic switches with one 10 Hz/7.6 ns pumping wave is demonstrated. Maximum energies at 3.05 μm, 4.25 μm, and 5.47 μm are 1.35 mJ, 1.03 mJ, and 0.56 mJ, respectively, corresponding to optical-to-optical conversion efficiencies of 9.4%, 7.6%, and 4.2%. To the best of our knowledge, this study is the first of generation of three mid-IR wavelength lasers using electro-optic switches. Furthermore, this study provides a viable solution for a high-energy or high-power, compact, or even portable multi-wavelength mid-IR laser device that employs a single pumping wave

    Rare deleterious germline variants and risk of lung cancer

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    Recent studies suggest that rare variants exhibit stronger effect sizes and might play a crucial role in the etiology of lung cancers (LC). Whole exome plus targeted sequencing of germline DNA was performed on 1045 LC cases and 885 controls in the discovery set. To unveil the inherited causal variants, we focused on rare and predicted deleterious variants and small indels enriched in cases or controls. Promising candidates were further validated in a series of 26,803 LCs and 555,107 controls. During discovery, we identified 25 rare deleterious variants associated with LC susceptibility, including 13 reported in ClinVar. Of the five validated candidates, we discovered two pathogenic variants in known LC susceptibility loci, ATM p.V2716A (Odds Ratio [OR] 19.55, 95%CI 5.04–75.6) and MPZL2 p.I24M frameshift deletion (OR 3.88, 95%CI 1.71–8.8); and three in novel LC susceptibility genes, POMC c.*28delT at 3′ UTR (OR 4.33, 95%CI 2.03–9.24), STAU2 p.N364M frameshift deletion (OR 4.48, 95%CI 1.73–11.55), and MLNR p.Q334V frameshift deletion (OR 2.69, 95%CI 1.33–5.43). The potential cancer-promoting role of selected candidate genes and variants was further supported by endogenous DNA damage assays. Our analyses led to the identification of new rare deleterious variants with LC susceptibility. However, in-depth mechanistic studies are still needed to evaluate the pathogenic effects of these specific alleles
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