74 research outputs found
BPCoach: Exploring Hero Drafting in Professional MOBA Tournaments via Visual Analytics
Hero drafting for multiplayer online arena (MOBA) games is crucial because
drafting directly affects the outcome of a match. Both sides take turns to
"ban"/"pick" a hero from a roster of approximately 100 heroes to assemble their
drafting. In professional tournaments, the process becomes more complex as
teams are not allowed to pick heroes used in the previous rounds with the
"best-of-N" rule. Additionally, human factors including the team's familiarity
with drafting and play styles are overlooked by previous studies. Meanwhile,
the huge impact of patch iteration on drafting strengths in the professional
tournament is of concern. To this end, we propose a visual analytics system,
BPCoach, to facilitate hero drafting planning by comparing various drafting
through recommendations and predictions and distilling relevant human and
in-game factors. Two case studies, expert feedback, and a user study suggest
that BPCoach helps determine hero drafting in a rounded and efficient manner.Comment: Accepted by The 2024 ACM SIGCHI Conference on Computer-Supported
Cooperative Work & Social Computing (CSCW) (Proc. CSCW 2024
Deformation-induced homogenization of the multi-phase senary high-entropy alloy MoNbTaTiVZr processed by high-pressure torsion
Dendritic microstructures are frequently observed in as-solidified refractory
high-entropy alloys (RHEAs), and their homogenization typically requires a
long-term heat treatment at extremely high temperatures. High-pressure torsion
(HPT) has been shown to be capable of mixing immiscible systems at room
temperature, and therefore represents a promising technique for homogenizing
dendritic RHEAs. In this work, the as-solidified RHEA MoNbTaTiVZr was processed
up to 40 revolutions by HPT. It was found that the dendritic microstructure was
eliminated, resulting in a chemical homogeneity at a von Mises equivalent shear
strain of about 400. The study of deformation mechanism showed an initial
strain localization, followed by a co-deformation of the dendritic and
interdendritic regions. In the co-deformation step, the Zr-rich interdendritic
region gradually disappeared. The deformation-induced mixing also led to the
formation of an ultra-fine grained (UFG) microstructure, exhibiting a grain
size of approximately 50 nm. The microhardness increased from 500 HV in the
as-solidified to 675 HV in the homogenized UFG state. The underlying mechanisms
responsible for the microhardness enhancement, such as grain refinement and
solid solution strengthening, were also discussed
PromotionLens: Inspecting Promotion Strategies of Online E-commerce via Visual Analytics
Promotions are commonly used by e-commerce merchants to boost sales. The
efficacy of different promotion strategies can help sellers adapt their
offering to customer demand in order to survive and thrive. Current approaches
to designing promotion strategies are either based on econometrics, which may
not scale to large amounts of sales data, or are spontaneous and provide little
explanation of sales volume. Moreover, accurately measuring the effects of
promotion designs and making bootstrappable adjustments accordingly remains a
challenge due to the incompleteness and complexity of the information
describing promotion strategies and their market environments. We present
PromotionLens, a visual analytics system for exploring, comparing, and modeling
the impact of various promotion strategies. Our approach combines
representative multivariant time-series forecasting models and well-designed
visualizations to demonstrate and explain the impact of sales and promotional
factors, and to support "what-if" analysis of promotions. Two case studies,
expert feedback, and a qualitative user study demonstrate the efficacy of
PromotionLens.Comment: IEEE Transactions on Visualization and Computer Graphics (Proc. IEEE
VIS 2022
Small RNA zippers lock miRNA molecules and block miRNA function in mammalian cells.
MicroRNAs (miRNAs) loss-of-function phenotypes are mainly induced by chemically modified antisense oligonucleotides. Here we develop an alternative inhibitor for miRNAs, termed \u27small RNA zipper\u27. It is designed to connect miRNA molecules end to end, forming a DNA-RNA duplex through a complementary interaction with high affinity, high specificity and high stability. Two miRNAs, miR-221 and miR-17, are tested in human breast cancer cell lines, demonstrating the 70∼90% knockdown of miRNA levels by 30-50 nM small RNA zippers. The miR-221 zipper shows capability in rescuing the expression of target genes of miR-221 and reversing the oncogenic function of miR-221 in breast cancer cells. In addition, we demonstrate that the miR-221 zipper attenuates doxorubicin resistance with higher efficiency than anti-miR-221 in human breast cancer cells. Taken together, small RNA zippers are a miRNA inhibitor, which can be used to induce miRNA loss-of-function phenotypes and validate miRNA target genes
YOLOv6: A Single-Stage Object Detection Framework for Industrial Applications
For years, the YOLO series has been the de facto industry-level standard for
efficient object detection. The YOLO community has prospered overwhelmingly to
enrich its use in a multitude of hardware platforms and abundant scenarios. In
this technical report, we strive to push its limits to the next level, stepping
forward with an unwavering mindset for industry application.
Considering the diverse requirements for speed and accuracy in the real
environment, we extensively examine the up-to-date object detection
advancements either from industry or academia. Specifically, we heavily
assimilate ideas from recent network design, training strategies, testing
techniques, quantization, and optimization methods. On top of this, we
integrate our thoughts and practice to build a suite of deployment-ready
networks at various scales to accommodate diversified use cases. With the
generous permission of YOLO authors, we name it YOLOv6. We also express our
warm welcome to users and contributors for further enhancement. For a glimpse
of performance, our YOLOv6-N hits 35.9% AP on the COCO dataset at a throughput
of 1234 FPS on an NVIDIA Tesla T4 GPU. YOLOv6-S strikes 43.5% AP at 495 FPS,
outperforming other mainstream detectors at the same scale~(YOLOv5-S, YOLOX-S,
and PPYOLOE-S). Our quantized version of YOLOv6-S even brings a new
state-of-the-art 43.3% AP at 869 FPS. Furthermore, YOLOv6-M/L also achieves
better accuracy performance (i.e., 49.5%/52.3%) than other detectors with a
similar inference speed. We carefully conducted experiments to validate the
effectiveness of each component. Our code is made available at
https://github.com/meituan/YOLOv6.Comment: technical repor
Isolation of exosomes from whole blood by integrating acoustics and microfluidics
Exosomes are nanoscale extracellular vesicles that play an important role in many biological processes, including intercellular communications, antigen presentation, and the transport of proteins, RNA, and other molecules. Recently there has been significant interest in exosome-related fundamental research, seeking new exosome-based biomarkers for health monitoring and disease diagnoses. Here, we report a separation method based on acoustofluidics (i.e., the integration of acoustics and microfluidics) to isolate exosomes directly from whole blood in a label-free and contact-free manner. This acoustofluidic platform consists of two modules: a microscale cell-removal module that first removes larger blood components, followed by extracellular vesicle subgroup separation in the exosome-isolation module. In the cell-removal module, we demonstrate the isolation of 110-nm particles from a mixture of micro- and nanosized particles with a yield greater than 99%. In the exosome-isolation module, we isolate exosomes from an extracellular vesicle mixture with a purity of 98.4%. Integrating the two acoustofluidic modules onto a single chip, we isolated exosomes from whole blood with a blood cell removal rate of over 99.999%. With its ability to perform rapid, biocompatible, label-free, contact-free, and continuous-flow exosome isolation, the integrated acoustofluidic device offers a unique approach to investigate the role of exosomes in the onset and progression of human diseases with potential applications in health monitoring, medical diagnosis, targeted drug delivery, and personalized medicine. Keywords: extracellular vesicles; exosomes; blood-borne vesicles; surface acoustic waves; acoustic tweezersNational Science Foundation (U.S.) (Grant R01 HD086325)National Science Foundation (U.S.) (Grant IIP-1534645
Application and research progress of antibody drug conjugates in HER2 positive advanced gastric cancer
Gastric cancer is a malignant tumor with high heterogeneity and invasiveness. Its incidence rate ranks fifth in the world, and its mortality ranks third in the world. Most patients are in a state that cancer cannot be removed by surgery when symptoms appear. At present, systemic treatment is the main treatment for advanced gastric cancer, and human epidermal growth factor receptor 2 (HER2) is one of the important treatment targets for HER2 positive gastric cancer patients. With the continuous optimization of chemotherapy regimen and targeted drugs, the prognosis of some HER2 positive gastric cancer patients has improved significantly. However, the high incidence of drug resistance and high toxicity and side effects are still the bottlenecks limiting the application of HER2 targeted drugs. Therefore, the development of new anti-tumor drugs is of great significance to improve the long-term survival of HER2 positive gastric cancer patients. Antibody drug conjugate (ADC) is a new and efficient anti-tumor drug, which is composed of specific targeted monoclonal antibody, chemical connector and small molecular cytotoxic payload. Its main advantages are strong therapeutic effect and moderate tissue toxicity. In recent years, ADC has set off a huge upsurge in the targeted treatment of HER2 positive advanced gastric cancer. First, after years of development, a variety of ADC including DS-8201 and RC48 have been used in the second- and second-line treatment of gastric cancer. Secondly, with the progress of ADC bioengineering technology, including high proportion of drug antibodies, cleavable linkers, toxic loads that can trigger bystander effect, the new type of ADC can play a more significant therapeutic role in the treatment of specific target tumors, and some of them also have multiple targets and can have anti-tumor effect on multiple specific targets. At the same time, the research and development process of ADC has reached the third stage. The new generation of ADC, through site-specific coupling technology, has higher homogeneity and uniformity, more effective cytotoxic molecules, higher accuracy and lower non-targeted toxicity. In addition, the "targeted immunotherapy" composed of ADC and immune checkpoint inhibitor (ICI) may be a promising treatment strategy for advanced gastric cancer. This article briefly reviewed the application and the latest research progress of ADC in HER2 positive advanced gastric cancer patients in the era of targeted therapy, and discussed the treatment prospects and challenges of ADC combined with ICI in HER2 positive advanced gastric cancer
Assessing causal associations between neurodegenerative diseases and neurological tumors with biological aging: a bidirectional Mendelian randomization study
BackgroundAging is a significant risk factor for many neurodegenerative diseases and neurological tumors. Previous studies indicate that the frailty index, facial aging, telomere length (TL), and epigenetic aging clock acceleration are commonly used biological aging proxy indicators. This study aims to comprehensively explore potential relationships between biological aging and neurodegenerative diseases and neurological tumors by integrating various biological aging proxy indicators, employing Mendelian randomization (MR) analysis.MethodsTwo-sample bidirectional MR analyses were conducted using genome-wide association study (GWAS) data. Summary statistics for various neurodegenerative diseases and neurological tumors, along with biological aging proxy indicators, were obtained from extensive meta-analyses of GWAS. Genetic single-nucleotide polymorphisms (SNPs) associated with the exposures were used as instrumental variables, assessing causal relationships between three neurodegenerative diseases (Alzheimer’s disease, Parkinson’s disease, amyotrophic lateral sclerosis), two benign neurological tumors (vestibular schwannoma and meningioma), one malignant neurological tumor (glioma), and four biological aging indicators (frailty index, facial aging, TL, and epigenetic aging clock acceleration). Sensitivity analyses were also performed.ResultsOur analysis revealed that genetically predicted longer TL reduces the risk of Alzheimer’s disease but increases the risk of vestibular schwannoma and glioma (All Glioma, GBM, non-GBM). In addition, there is a suggestive causal relationship between some diseases (PD and GBM) and DNA methylation GrimAge acceleration. Causal relationships between biological aging proxy indicators and other neurodegenerative diseases and neurological tumors were not observed.ConclusionBuilding upon prior investigations into the causal relationships between telomeres and neurodegenerative diseases and neurological tumors, our study validates these findings using larger GWAS data and demonstrates, for the first time, that Parkinson’s disease and GBM may promote epigenetic age acceleration. Our research provides new insights and evidence into the causal relationships between biological aging and the risk of neurodegenerative diseases and neurological tumors
Molecular Engineered Hole-Extraction Materials to Enable Dopant-Free, Efficient p-i-n Perovskite Solar Cells
Two hole-extraction materials (HEMs), TPP-OMeTAD and TPP-SMeTAD, have been developed to facilitate the fabrication of efficient p-i-n perovskite solar cells (PVSCs). By replacing the oxygen atom on HEM with sulfur (from TPP-OMeTAD to TPP-SMeTAD), it effectively lowers the highest occupied molecular orbital of the molecule and provides stronger Pb-S interaction with perovskites, leading to efficient charge extraction and surface traps passivation. The TPP-SMeTAD-based PVSCs exhibit both improved photovoltaic performance and reduced hysteresis in p-i-n PVSCs over those based on TPP-OMeTAD. This work not only provides new insights on creating perovskite-HEM heterojunction but also helps in designing new HEM to enable efficient organic–inorganic hybrid PVSCs
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