检索结果-内蒙古大学图书馆

arXiv 2024年

作者： Sumner, Jacob Meng, Grace Brandt, Naomi Grigas, Alex T. Córdoba, Andrés Shattuck, Mark D. O’Hern, Corey S. Graduate Program in Computational Biology and Bioinformatics Yale University New HavenCT06520 United States Integrated Graduate Program in Physical and Engineering Biology Yale University New HavenCT06520 United States Department of Chemistry Yale University New HavenCT06520 United States Department of Physics Yale University New HavenCT06520 United States Department of Chemistry Duke University DurhamNC27708 United States Department of Physics Duke University DurhamNC27708 United States Benjamin Levich Institute Physics Department City College of New York New YorkNY10031 United States Department of Mechanical Engineering and Materials Science Yale University New HavenCT06520 United States Department of Applied Physics Yale University New HavenCT06520 United States

A goal of computational studies of protein-protein interfaces (PPIs) is to predict the binding site between two monomers that form a heterodimer. The simplest version of this problem is to rigidly re-dock the bound forms of the monomers, which involves generating computational models of the heterodimer and then scoring them to determine the most native-like models. Scoring functions have been assessed previously using rank- and classification-based metrics, however, these methods are sensitive to the number and quality of models in the scoring function training set. We assess the accuracy of seven PPI scoring functions by comparing their scores to a measure of structural similarity to the x-ray crystal structure (i.e. the DockQ score) for a non-redundant set of heterodimers from the Protein Data Bank. For each heterodimer, we generate re-docked models uniformly sampled over DockQ and calculate the Spearman correlation between the PPI scores and DockQ. For some targets, the scores and DockQ are highly correlated;however, for many targets, there are weak correlations. Several physical features can explain the difference between difficult- and easy-to-score targets. For example, strong correlations exist between the score and DockQ for targets with highly intertwined monomers and many interface contacts. We also develop a new score based on only three physical features that matches or exceeds the performance of current PPI scoring functions. These results emphasize that PPI prediction can be improved by focusing on correlations between the PPI score and DockQ and incorporating more discriminating physical features into PPI scoring functions. © 2024, CC BY.

关键词： Monomers

来源：评论

学校读者我要写书评

暂无评论

A machine learning-based high-precision density functional method for drug-like molecules

Artificial Intelligence Chemistry

引用

Artificial Intelligence Chemistry 2024年第1期2卷

作者： Jin Xiao YiXiao Chen LinFeng Zhang Han Wang Tong Zhu Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development Shanghai Frontiers Science Center of Molecule Intelligent Syntheses School of Chemistry and Molecular Engineering East China Normal University Shanghai 200062 P.R. China Program in Applied and Computational Mathematics Princeton University Princeton NJ 08544 USA AI for Science Institute Beijing 100080 P.R. China Laboratory of Computational Physics Institute of Applied Physics and Computational Mathematics Beijing 100088 P.R. China NYU-ECNU Center for Computational Chemistry at NYU Shanghai Shanghai 200062 P.R. China Shenzhen Institute of Advanced Technology Chinese Academy of Sciences Shenzhen 518005 P.R. China

In computer-aided drug discovery, accurately determining the structure and properties of drug-like molecules is of utmost importance. This necessitates the use of precise and efficient electronic structure methods. Here, we developed two deep learning-based density functional methods, namely DeePHF and DeePKS, specifically tailored for drug-like molecules. Notably, DeePKS incorporates self-consistency into its framework. With a limited dataset labelled at the CCSD(T)/def2-TZVP level, both models have been able to achieve chemical accuracy in calculating molecular energies and have demonstrated excellent transferability. We anticipate that further advancements in this field will lead to the development of high-quality density functional methods designed specifically for drug discovery purposes. This research showcases the capabilities of deep learning approaches in simplifying the construction complexity associated with traditional DFT methods.

关键词： Machine Learning Density Functional Theory DeePHF DeePKS

来源：评论

学校读者我要写书评

暂无评论

A Brief Review of Explainable Artificial Intelligence in Healthcare

arXiv

引用

arXiv 2023年

作者： Sadeghi, Zahra Alizadehsani, Roohallah Cifci, Mehmet Akif Kausar, Samina Rehman, Rizwan Mahanta, Priyakshi Bora, Pranjal Kumar Almasri, Ammar Alkhawaldeh, Rami S. Hussain, Sadiq Alatas, Bilal Shoeibi, Afshin Moosaei, Hossein Hladík, Milan Nahavandi, Saeid Pardalos, Panos M. Institute for Big Data Analytics Faculty of Computer Science Dalhousie University Canada Deakin University Geelong Australia The Institute of Computer Technology Tu Wien University Vienna1040 Austria University of Kotli Azad Jammu and Kashmir Azad Kashmir Kotli Pakistan Centre for Computer Science and Applications Dibrugarh University Assam India Department of Management Information Sys Al-Balqa Applied University Salt19117 Jordan Department of Computer Information Systems The University of Jordan Aqaba77110 Jordan Examination Branch Dibrugarh University Assam Dibrugarh India Department of Software Eng. Firat University Elazig23100 Turkey Data Science and Computational Intelligence Institute University of Granada Spain Department of Informatics Faculty of Science Jan Evangelista Purkyně University in Ústí nad Labem Czech Republic Department of Applied Mathematics School of Computer Science Faculty of Mathematics and Physics Charles University Prague Czech Republic Harvard Paulson School of Engineering and Applied Sciences Harvard University AllstonMA02134 United States Center for Applied Optimization Department of Industrial and Systems Engineering University of Florida Gainesville32611 United States

XAI refers to the techniques and methods for building AI applications which assist end users to interpret output and predictions of AI models. Black box AI applications in high-stakes decision-making situations, such as medical domain have increased the demand for transparency and explainability since wrong predictions may have severe consequences. Model explainability and interpretability are vital successful deployment of AI models in healthcare practices. AI applications' underlying reasoning needs to be transparent to clinicians in order to gain their trust. This paper presents a systematic review of XAI aspects and challenges in the healthcare domain. The primary goals of this study are to review various XAI methods, their challenges, and related machine learning models in healthcare. The methods are discussed under six categories: Features-oriented methods, global methods, concept models, surrogate models, local pixel-based methods, and human-centric methods. Most importantly, the paper explores XAI role in healthcare problems to clarify its necessity in safety-critical applications. The paper intends to establish a comprehensive understanding of XAI-related applications in the healthcare field by reviewing the related experimental results. To facilitate future research for filling research gaps, the importance of XAI models from different viewpoints and their limitations are investigated. © 2023, CC BY-NC-ND.

关键词： Decision making

来源：评论

学校读者我要写书评

暂无评论

High-temperature mid-IR absorption and reaction kinetics of 2-methyl-1,3-dioxolane: An experimental and theoretical study

引用

Journal of Photochemistry and Photobiology 2023年 13卷

作者： Adil, Mohammad Giri, Binod Raj Mai, Tam V.-T. Szőri, Milán Huynh, Lam K. Farooq, Aamir Mechanical Engineering Program Physical Science and Engineering Division King Abdullah University of Science and Technology (KAUST) Thuwal 23955-6900 Saudi Arabia KAUST Clean Combustion Research Center King Abdullah University of Science and Technology Saudi Arabia Molecular Science and Nano-Materials Lab Institute for Computational Science and Technology SBI Building Quang Trung Software City Tan Chanh Hiep Ward District 12 Ho Chi Minh Viet Nam University of Science Vietnam National University – HCMC 227 Nguyen Van Cu Ward 4 District 5 Ho Chi Minh Viet Nam Vietnam National University – HCMC Quarter 6 Linh Trung Ward Thu Duc Ho Chi Minh Viet Nam Institute of Chemistry University of Miskolc Egyetemváros A/2 Miskolc H-3515 Hungary School of Chemical and Environmental Engineering International University Quarter 6 Linh Trung Ward Thu Duc City Ho Chi Minh City Viet Nam

This work reports the mid-IR spectroscopy and reaction kinetics of 2-methyl-1,3-dioxolane (2M13DO). We carried out spectroscopic measurements to deduce temperature-dependent absorption cross-sections of 2M13DO over a broad wavelength range of 8.4–10.5 μm (950–1190 cm⁻¹). For these measurements, we employed a rapidly tuning MIRcat-QT™ laser that can be operated either at a fixed wavelength or scanned mode over wide wavelength regions. By operating the laser at a fixed wavelength, we monitored the decay of 2M13DO behind reflected shock waves over T₅ = 1050–1400 K and P₅ = 0.7 and 2.6 bar. Our measured concentration time-histories of 2M13DO allowed us to directly extract the overall rate coefficients for the unimolecular decomposition of 2M13DO using the first-order rate law. We did not observe any pressure dependence in the measured rate coefficients, indicating that the reaction is close to the high-pressure limit. By employing the W1U composite method, we explored the important pyrolysis reaction pathways of 2M13DO in the reactive potential energy surface. Three important reaction channels, namely, 2M13DO → CH₂[dbnd]CHOCH₂CH₂OH (IM1), 2M13DO → 2CH₃CHO (P3), 2M13DO → CH₃ + 1,3-dioxolan-2-yl (P4) were identified. Below 700 K, IM1 forming channel is dominant, whereas CH₃CHO formation is dominant under our experimental conditions. Above 1500 K, the radical forming channel (CH₃+P4) takes over other channels. At higher temperatures, the contribution of the radical forming channel continually increases, accounting for ∼ 99% at 2000 K. We used the stochastic RRKM-ME model to predict the pressure and temperature dependence of the rate coefficients, k(T, P), and time-resolved species profiles. Our theory showed excellent agreement with the measured rate coefficients. These are the first direct determination of the rate coefficients of the unimolecular decomposition of

关键词： 2-Methyl-1,3-dioxolane Absorption spectra High-temperature Pyrolysis RRKM-ME calculations Shock tube

来源：评论

学校读者我要写书评

暂无评论

An Open-Source Knowledge Graph Ecosystem for the Life sciences

arXiv

引用

arXiv 2023年

作者： Callahan, Tiffany J. Tripodi, Ignacio J. Stefanski, Adrianne L. Cappelletti, Luca Taneja, Sanya B. Wyrwa, Jordan M. Casiraghi, Elena Matentzoglu, Nicolas A. Reese, Justin Silverstein, Jonathan C. Hoyt, Charles Tapley Boyce, Richard D. Malec, Scott A. Unni, Deepak R. Joachimiak, Marcin P. Robinson, Peter N. Mungall, Christopher J. Cavalleri, Emanuele Fontana, Tommaso Valentini, Giorgio Mesiti, Marco Gillenwater, Lucas A. Santangelo, Brook Vasilevsky, Nicole A. Hoehndorf, Robert Bennett, Tellen D. Ryan, Patrick B. Hripcsak, George Kahn, Michael G. Bada, Michael Baumgartner, William A. Hunter, Lawrence E. Computational Bioscience Program University of Colorado Anschutz Medical Campus AuroraCO80045 United States Department of Biomedical Informatics Columbia University Irving Medical Center New YorkNY10032 United States Computer Science Department Interdisciplinary Quantitative Biology University of Colorado Boulder BoulderCO80301 United States AnacletoLab Computer Science Department University of Milan 20122 Italy Intelligent Systems Program University of Pittsburgh PittsburghPA15260 United States Department of Physical Medicine and Rehabilitation School of Medicine University of Colorado Anschutz Medical Campus AuroraCO80045 United States Division of Environmental Genomics and Systems Biology Lawrence Berkeley National Laboratory BerkeleyCA94720 United States Semanticly Ltd Athens Greece Department of Biomedical Informatics University of Pittsburgh School of Medicine PittsburghPA15206 United States Laboratory of Systems Pharmacology Harvard Medical School BostonMA02115 United States Division of Translational Informatics University of New Mexico School of Medicine AlbuquerqueNM87131 United States SIB Swiss Institute of Bioinformatics Basel Switzerland Berlin Institute of Health at Charité-Universitatsmedizin Berlin10117 Germany ELLIS European Laboratory for Learning and Intelligent Systems Germany Department of Biomedical Informatics University of Colorado School of Medicine AuroraCO80045 United States Data Collaboration Center Critical Path Institute 1840 E River Rd. Suite 100 TucsonAZ85718 United States Computer Electrical and Mathematical Sciences & Engineering Division Computational Bioscience Research Center King Abdullah University of Science and Technology Thuwal23955-6900 Saudi Arabia Department of Pediatrics University of Colorado School of Medicine AuroraCO80045 United States Janssen Research and Development RaritanNJ08869 United States Division of General Internal Medicine University of Colorado School of Medicine A

Translational research requires data at multiple scales of biological organization. Advancements in sequencing and multi-omics technologies have increased the availability of these data, but researchers face significant integration challenges. Knowledge graphs (KGs) are used to model complex phenomena, and methods exist to construct them automatically. However, tackling complex biomedical integration problems requires flexibility in the way knowledge is modeled. Moreover, existing KG construction methods provide robust tooling at the cost of fixed or limited choices among knowledge representation models. PheKnowLator (Phenotype Knowledge Translator) is a semantic ecosystem for automating the FAIR (Findable, Accessible, Interoperable, and Reusable) construction of ontologically grounded KGs with fully customizable knowledge representation. The ecosystem includes KG construction resources (e.g., data preparation APIs), analysis tools (e.g., SPARQL endpoints and abstraction algorithms), and benchmarks (e.g., prebuilt KGs and embeddings). We evaluated the ecosystem by systematically comparing it to existing open-source KG construction methods and by analyzing its computational performance when used to construct 12 large-scale KGs. With flexible knowledge representation, PheKnowLator enables fully customizable KGs without compromising performance or usability. © 2023, CC BY.

关键词： Ecosystems

来源：评论

学校读者我要写书评

暂无评论

TARGET SPECIFIC DE NOVO DESIGN OF DRUG CANDIDATE MOLECULES WITH GRAPH TRANSFORMER-BASED GENERATIVE ADVERSARIAL NETWORKS

arXiv

引用

arXiv 2023年

作者： Ünlü, Atabey Çevrim, Elif Sarıgün, Ahmet Yiğit, Melih Gökay Çelikbilek, Hayriye Bayram, Osman Güvenilir, Heval Ataş Koyaş, Altay Kahraman, Deniz Cansen Olğaç, Abdurrahman Rifaioğlu, Ahmet Banoğlu, Erden Doğan, Tunca Biological Data Science Lab Dept. of Computer Engineering Hacettepe University Turkey Dept. of Bioinformatics Graduate School of Health Sciences Hacettepe University Turkey Dept. of Chemistry Middle East Technical University Turkey Dept. of Physics Middle East Technical University Turkey Dept. of Computer Engineering Middle East Technical University Turkey Dept. Of Artificial Intelligence Engineering Bahcesehir University Turkey Cancer Systems Biology Lab Graduate School of Informatics Middle East Technical University Turkey Dept. of Pharmaceutical Chemistry Faculty of Pharmacy Gazi University Turkey Laboratory of Molecular Modeling Evias Pharmaceutical R&D Ltd Turkey Dept. of Electrical and Electronics Engineering Iskenderun Technical University Turkey Institute for Computational Biomedicine Heidelberg University Germany

Discovering novel drug candidate molecules is one of the most fundamental and critical steps in drug development. Generative deep learning models, which create synthetic data given a probability distribution, offer a high potential for designing de novo molecules. However, for them to be useful in real-life drug development pipelines, these models should be able to design drug-like and target-centric molecules. In this study, we propose an end-to-end generative system, DrugGEN, for the de novo design of drug candidate molecules that interact with intended target proteins. The proposed method represents molecules as graphs and processes them via a generative adversarial network comprising graph transformer layers. The system is trained using a large dataset of drug-like compounds and target-specific bioactive molecules to design effective inhibitory molecules against the AKT1 protein, which is critically important in developing treatments for various types of cancer. We conducted molecular docking and dynamics to assess the target-centric generation performance of the model, as well as attention score visualisation to examine model interpretability. Results indicate that our de novo molecules have a high potential for interacting with the AKT1 protein at the level of its native ligands. Using the open-access DrugGEN codebase, it is possible to easily train models for other druggable proteins, given a dataset of experimentally known bioactive molecules. © 2023, CC BY-NC-SA.

关键词： Generative adversarial networks

来源：评论

学校读者我要写书评

暂无评论

Feasibility of Inferring Spatial Transcriptomics from Single-Cell Histological Patterns for Studying Colon Cancer Tumor Heterogeneity

Feasibility of Inferring Spatial Transcriptomics from Single...

引用

18th International Joint Conference on Biomedical engineering Systems and Technologies, BIOSTEC 2025

作者： Fatemi, Michael Y. Lu, Yunrui Azher, Zarif L. Sharma, Cyril Feng, Eric Diallo, Alos B. Srinivasan, Gokul Rosner, Grace M. Pointer, Kelli B. Christensen, Brock C. Salas, Lucas A. Tsongalis, Gregory J. Palisoul, Scott M. Perreard, Laurent Kolling, Fred W. Vaickus, Louis J. Levy, Joshua J. University of Virginia CharlottesvilleVA United States Emerging Diagnostic and Investigative Technologies Department of Pathology and Laboratory Medicine Dartmouth Health LebanonNH United States Department of Computer Science Purdue University West LafayetteIN United States Thomas Jefferson High School for Science and Technology AlexandriaVA United States Department of Epidemiology Dartmouth College Geisel School of Medicine HanoverNH United States Program in Quantitative Biomedical Sciences Dartmouth College Geisel School of Medicine HanoverNH United States Department of Medicine Section of Radiology Oncology Dartmouth Health LebanonNH United States Department of Molecular and Cell Biology Dartmouth College Geisel School of Medicine HanoverNH United States Genomics Shared Resource Dartmouth Cancer Center LebanonNH United States Department of Dermatology Dartmouth Health LebanonNH United States Department of Pathology and Laboratory Medicine Cedars Sinai Medical Center Los AngelesCA United States Department of Computational Biomedicine Cedars Sinai Medical Center Los AngelesCA United States Division of Biology and Biological Engineering California Institute of Technology PasadenaCA United States

Spatial transcriptomics (ST) enables studying spatial organization of gene expression within tissues, offering insights into the molecular diversity of tumors. Recent methods have demonstrated the capability to disaggregate this information at subspot resolution by leveraging both expression and histological patterns. Elucidating such information from histology alone presents a significant challenge, but if solved can enable spatial molecular analysis at cellular resolution even where ST data is not available, reducing study costs. This study explores integrating single-cell histological and transcriptomic data to infer spatial mRNA expression patterns in colorectal cancer whole slide images. A cell-graph neural network algorithm was developed to align histological information extracted from detected cells with single cell RNA, facilitating the analysis of cellular groupings and gene relationships. We demonstrate that single-cell transcriptional heterogeneity within a spot could be predicted from histological markers extracted from cells detected within it. Our model exhibited proficiency in delineating overarching gene expression patterns across whole-slide images. This approach compared favorably to traditional computer vision methods which did not incorporate single cell expression during the model training. This innovative approach augments the resolution of spatial molecular assays utilizing histology as sole input through co-mapping of histological and transcriptomic datasets at the single-cell level. © 2025 by SCITEPRESS– science and Technology Publications, Lda.

关键词： Tumors

来源：评论

学校读者我要写书评

暂无评论

L3C-Stereo: Lossless compression for stereo images

arXiv

引用

arXiv 2021年

作者： Huang, Zihao Sun, Zhe Duan, Feng Cichocki, Andrzej Ruan, Peiying Li, Chao College of Artificial Intelligence Nankai University Tianjin China Computational Engineering Applications Unit Office for Information Systems and Cybersecurity RIKEN Saitama Japan Skolkovo Institute of Science and Technology Moscow Russia College of Computer Science Hangzhou Dianzi University China Department of Informatics Nicolaus Copernicus University Poland Systems Research Institute of Polish of Academy of Science Warsaw Poland NVIDIA AI Technology Center NVIDIA Corporation Japan Japan RIKEN Japan

A large number of autonomous driving tasks need high-definition stereo images, which requires a large amount of storage space. Efficiently executing lossless compression has become a practical problem. Commonly, it is hard to make accurate probability estimates for each pixel. To tackle this, we propose L3C-Stereo, a multi-scale lossless compression model consisting of two main modules: the warping module and the probability estimation module. The warping module takes advantage of two view feature maps from the same domain to generate a disparity map, which is used to reconstruct the right view so as to improve the confidence of the probability estimate of the right view. The probability estimation module provides pixelwise logistic mixture distributions for adaptive arithmetic coding. In the experiments, our method outperforms the hand-crafted compression methods and the learning-based method on all three datasets used. Then, we show that a better maximum disparity can lead to a better compression effect. Furthermore, thanks to a compression property of our model, it naturally generates a disparity map of an acceptable quality for the subsequent stereo tasks. © 2021, CC BY.

关键词： Stereo image processing

来源：评论

学校读者我要写书评

暂无评论

Adaptive Traffic Signal Control for Developing Countries Using Fused Parameters Derived from Crowd-Source Data

arXiv

引用

arXiv 2022年

作者： Mishra, Sumit Singh, Vishal Gupta, Ankit Bhattacharya, Devanjan Mudgal, Abhisek The Robotics Program Korea Advanced Institute of Science and Technology Daejeon Korea Republic of Member of Technical Staff VMware Inc Palo AltoCA United States Department of Civil Engineering Indian Institute of Technology Banaras Hindu University Varanasi India Marie Sklodowska-Curie Actions TRAIN@ED School of Law School of Informatics University of Edinburgh United Kingdom Universidade Nova de Lisboa Campus de Campolide Lisboa1070-312 Portugal

Advancement of mobile technologies has enabled economical collection, storage, processing, and sharing of traffic data. These data are made accessible to intended users through various application program interfaces (API) and can be used to recognize and mitigate congestion in real time. In this paper, quantitative (time of arrival) and qualitative (color-coded congestion levels) data were acquired from the Google traffic APIs. New parameters that reflect heterogeneous traffic conditions were defined and utilized for real-time control of traffic signals while maintaining the green-to-red time ratio. The proposed method utilizes a congestion-avoiding principle commonly used in computer networking. Adaptive congestion levels were observed on three different intersections of Delhi (India), in peak hours. It showed good variation, hence sensitive for the control algorithm to act efficiently. Also, simulation study establishes that proposed control algorithm decreases waiting time and congestion. The proposed method provides an inexpensive alternative for traffic sensing and tracking technologies. © 2022, CC BY.

关键词： Crowdsourcing

来源：评论

学校读者我要写书评

暂无评论

Question-Answering System Extracts Information on Injection Drug Use from Clinical Notes

arXiv

引用

arXiv 2023年

作者： Mahbub, Maria Goethert, Ian Danciu, Ioana Knight, Kathryn Srinivasan, Sudarshan Tamang, Suzanne Rozenberg-Ben-Dror, Karine Solares, Hugo Martins, Susana Trafton, Jodie Begoli, Edmon Peterson, Gregory D. Cyber Resilience and Intelligence Division Oak Ridge National Laboratory Oak RidgeTN United States Information Technology Services Division Oak Ridge National Laboratory Oak RidgeTN United States Computational Sciences and Engineering Division Oak Ridge National Laboratory Oak RidgeTN United States Department of Biomedical Informatics Vanderbilt University NashvilleTN United States Program Evaluation and Resource Center Office of Mental Health and Suicide Prevention Department of Veterans Affairs United States Department of Medicine Stanford University School of Medicine StanfordCA United States Veterans Affairs Great Lakes Health Care System WestchesterIL United States Department of Electrical Engineering and Computer Science University of Tennessee Knoxville KnoxvilleTN United States

Background: Injection drug use (IDU) is a dangerous health behavior that increases mortality and morbidity. Identifying IDU early and initiating harm reduction interventions can benefit individuals at risk. However, extracting IDU behaviors from patients’ electronic health records (EHR) is difficult because there is no International Classification of Disease (ICD) code and the only place IDU information can be indicated is unstructured free-text clinical notes. Although natural language processing can efficiently extract this information from unstructured data, there are no validated tools. Methods: To address this gap in clinical information, we design and demonstrate a question-answering (QA) framework to extract information on IDU from clinical notes. Our framework involves two main steps: (1) generating a gold-standard QA dataset and (2) developing and testing the QA model. We utilize 2323 clinical notes of 1145 patients sourced from the VA Corporate Data Warehouse to construct the gold-standard dataset for developing and evaluating the QA model. We also demonstrate the QA model’s ability to extract IDU-related information on temporally out-of-distribution data. Results: Here we show that for a strict match between gold-standard and predicted answers, the QA model achieves 51.65% F1 score. For a relaxed match between the gold-standard and predicted answers, the QA model obtains 78.03% F1 score, along with 85.38% Precision and 79.02% Recall scores. Moreover, the QA model demonstrates consistent performance when subjected to temporally out-of-distribution data. Conclusions: Our study introduces a QA framework designed to extract IDU information from clinical notes, aiming to enhance the accurate and efficient detection of people who inject drugs, extract relevant information, and ultimately facilitate informed patient care. © 2023, CC BY-NC-ND.

关键词： Data warehouses

来源：评论

学校读者我要写书评

暂无评论

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

请选择保存的检索档案：

请选择收藏分类：

通借通还

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：