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Experimental and real-world evidence supporting the computational repurposing of bumetanide for APOE4-related Alzheimer's disease ( Oct, 10.1038/s43587-021-00122-7, 2021)

NATURE AGING

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NATURE AGING 2021年第12期1卷 1202-1202页

作者： Taubes, Alice Nova, Phil Zalocusky, Kelly A. Kosti, Idit Bicak, Mesude Zilberter, Misha Y. Hao, Yanxia Yoon, Seo Yeon Oskotsky, Tomiko Pineda, Silvia Chen, Bin Jones, Emily Aery A. Choudhary, Krishna Grone, Brian Balestra, Maureen E. Chaudhry, Fayzan Paranjpe, Ishan De Freitas, Jessica Koutsodendris, Nicole Chen, Nuo Wang, Celine Chang, William An, Alice Glicksberg, Benjamin S. Sirota, Marina Huang, Yadong Gladstone Institute of Neurological Disease Gladstone Institutes San Francisco CA USA Biomedical Sciences Graduate Program University of California San Francisco CA USA Gladstone Center for Translational Advancement Gladstone Institutes San Francisco CA USA Department of Neurology University of California San Francisco CA USA Bakar Computational Health Sciences Institute University of California San Francisco CA USA Department of Pediatrics University of California San Francisco CA USA Hasso Plattner Institute for Digital Health at Mount Sinai Icahn School of Medicine at Mount Sinai New York NY USA Department of Genetics and Genomic Sciences Icahn School of Medicine at Mount Sinai New York NY USA Department of Surgery University of California San Francisco CA USA Gladstone Institute of Data Science and Biotechnology Gladstone Institutes San Francisco CA USA Development and Stem Cell Biology Graduate Program University of California San Francisco CA USA Department of Pathology University of California San Francisco CA USA

The evident genetic, pathological and clinical heterogeneity of Alzheimer’s disease (AD) poses challenges for traditional drug development. We conducted a computational drug-repurposing screen for drugs to treat apolipoprotein E4 (APOE4)-related AD. We first established APOE genotype-dependent transcriptomic signatures of AD by analyzing publicly available human brain databases. We then queried these signatures against the Connectivity Map database, which contains transcriptomic perturbations of more than 1,300 drugs, to identify those that best reverse APOE genotype-specific AD signatures. Bumetanide was identified as a top drug for APOE4-related AD. Treatment of APOE4-knock-in mice without or with amyloid β (Aβ) accumulation using bumetanide rescued electrophysiological, pathological or cognitive deficits. Single-nucleus RNA sequencing revealed transcriptomic reversal of AD signatures in specific cell types in these mice, a finding confirmed in APOE4 induced pluripotent stem cell (iPSC)-derived neurons. In humans, bumetanide exposure was associated with a significantly lower AD prevalence in individuals over the age of 65 years in two electronic health record databases, suggesting the effectiveness of bumetanide in preventing AD.

关键词： Ageing Alzheimer's disease computational neuroscience Life Sciences general

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Multicenter target trial emulation to evaluate corticosteroids for sepsis stratified by predicted organ dysfunction trajectory

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Nature Communications 2025年第1期16卷 1-10页

作者： Rajendran, Suraj Xu, Zhenxing Pan, Weishen Zang, Chengxi Siempos, Ilias Torres, Lisa Xu, Jie Bian, Jiang Schenck, Edward J. Wang, Fei Tri-Institutional Computational Biology & Medicine Program Cornell University Cornell NY United States Division of Health Informatics Department of Population Health Sciences Weill Cornell Medicine New York NY United States Division of Pulmonary and Critical Care Medicine Department of Medicine New York-Presbyterian Hospital-Weill Cornell Medical Center Weill Cornell Medicine New York NY United States First Department of Critical Care Medicine and Pulmonary Services Evangelismos Hospital National and Kapodistrian University of Athens Medical School Athens Greece Department of Health Outcomes and Biomedical Informatics College of Medicine University of Florida Gainesville FL United States Department of Biostatistics and Health Data Science School of Medicine Indiana University Indianapolis IN United States Regenstrief Institute Indianapolis IN United States

Corticosteroids decrease the duration of organ dysfunction in sepsis and a range of overlapping and complementary infectious critical illnesses, including septic shock, pneumonia and the acute respiratory distress syndrome (ARDS). The risk and benefit of corticosteroids are not fully defined using the construct of organ dysfunction duration. This retrospective multicenter, proof-of-concept study aimed to evaluate the association between usage of corticosteroids and mortality of patients with sepsis, pneumonia and ARDS by emulating a target trial framework stratified by predicted organ dysfunction trajectory. The study employed a two staged machine learning (ML) methodology to first subphenotype based on organ dysfunction trajectory then predict this defined trajectory. Once patients were classified by predicted trajectory we conducted a target trial emulation. Our analysis revealed that the association between corticosteroid use and 28-day mortality varied by predicted trajectory and between *** findings suggest that matching treatment strategies to empirically observed pathobiology may offer a more nuanced understanding of corticosteroid utility. © The Author(s) 2025.

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biomedical data and AI

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Science China Life Sciences 2025年第5期68卷 1536-1540页

作者： Hao Xu Shibo Zhou Zefeng Zhu Vincenzo Vitelli Liangyi Chen Ziwei Dai Ning Yang Luhua Lai Shengyong Yang Sergey Ovchinnikov Zhuoran Qiao Sirui Liu Chen Song Jianfeng Pei Han Wen Jianfeng Feng Yaoyao Zhang Zhengwei Xie Yang-Yu Liu Zhiyuan Li Fulai Jin Hao Li Mohammad Lotfollahi Xuegong Zhang Ge Yang Shihua Zhang Ge Gao Pulin Li Qi Liu Jing-Dong Jackie Han Peking-Tsinghua Center for Life Sciences (CLS) Academy for Advanced Interdisciplinary StudiesPeking University Center for Quantitative Biology (CQB) Academy for Advanced Interdisciplinary StudiesPeking University Peking University-Tsinghua University-National Institute of Biological Sciences Joint Graduate Program Academy for Advanced Interdisciplinary StudiesPeking University Department of Physics University of Chicago School of Life Sciences Southern University of Science and Technology Peking University Chengdu Academy for Advanced Interdisciplinary Biotechnologies College of Chemistry and Molecular Engineering Peking University Department of Biotherapy Cancer Center and State Key Laboratory of BiotherapyWest China HospitalSichuan University Department of Biology Massachusetts Institute of Technology Lambic Therapeutics Inc. Changping Laboratory Al for Science Institute Key Laboratory of Computational Neuroscience and Brain-Inspired Intelligence Fudan University Department of Obstetrics and Gynecology West China Second University HospitalSichuan University Peking University International Cancer Institute and Peking University-Yunnan Baiyao International Medical Institute and State Key Laboratory of Natural and Biomimetic Drugs Department of Molecular and Cellular PharmacologySchool of Pharmaceutical SciencesPeking University Health Science CenterPeking University Channing Division of Network Medicine Department of MedicineBrigham and Women's Hospital and Harvard Medical School Center for Artificial Intelligence and Modeling the Carl R.Woese Institute for Genomic BiologyUniversity of Illinois Urbana-Champaign Department of Genetics and Genome Sciences School of Medicine and Department of Computer and Data Sciences and Department of Population and Quantitative Health SciencesCase Western Reserve University Department of Biochemistry and Biophysics University of California Sanger Institute Department of Automation Tsinghua University State Key Laboratory of Multimodal Artificial Intelligence Systems I

The development of artificial intelligence(AI) and the mining of biomedical data complement each other. From the direct use of computer vision results to analyze medical images for disease screening, to now integrating biological knowledge into models and even accelerating the development of new AI based on biological discoveries, the boundaries of both are constantly expanding, and their connections are becoming closer.

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Uncertainty abounds, what now?

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Science 2025年第6740期387卷 1261页

作者： Dov Greenbaum Mark Gerstein The reviewer is at the Zvi Meitar Institute for Legal Implications of Emerging Technologies The reviewer is at the Harry Radzyner Law School The reviewer is at the Dina Recanati School of Medicine Reichman University Herzliya Israel The reviewer is at the Department of Biomedical Informatics and Data Science The reviewer is at the Program in Computational Biology and Bioinformatics The reviewer is at the Department of Computer Science Yale University New Haven CT USA.

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Random-effects substitution models for phylogenetics via scalable gradient approximations

arXiv

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arXiv 2023年

作者： Magee, Andrew F. Holbrook, Andrew J. Pekar, Jonathan E. Caviedes-Solis, Itzue W. Matsen, Fredrick A. Baele, Guy Wertheim, Joel O. Ji, Xiang Lemey, Philippe Suchard, Marc A. Department of Biostatistics Jonathan and Karin Fielding School of Public Health University of California Los Angeles Los AngelesCA United States Bioinformatics and Systems Biology Graduate Program University of California San Diego La Jolla CA United States Department of Biomedical Informatics University of California San Diega La Jolla CA United States Department of Biology Swarthmore College SwarthmorePA United States Howard Hughes Medical Institute SeattleWA United States Computational Biology Program Fred Hutchinson Cancer Research Center SeattleWA United States Department of Genome Sciences University of Washington SeattleWA United States Department of Statistics University of Washington SeattleWA United States Department of Microbiology Immunology and Transplantation Rega Institute KU Leuven Leuven Belgium Department of Medicine University of California San Diego La Jolla CA United States Department of Mathematics Tulane University New OrleansLA United States Department of Biomathematics David Geffen School of Medicine at UCLA University of California Los Angeles Los AngelesCA United States Department of Human Genetics David Geffen School of Medicine at UCLA Universtiy of California Los Angeles Los AngelesCA United States

Phylogenetic and discrete-trait evolutionary inference depend heavily on an appropriate characterization of the underlying character substitution process. In this paper, we present random-effects substitution models that extend common continuous-time Markov chain models into a richer class of processes capable of capturing a wider variety of substitution dynamics. As these random-effects substitution models often require many more parameters than their usual counterparts, inference can be both statistically and computationally challenging. Thus, we also propose an efficient approach to compute an approximation to the gradient of the data likelihood with respect to all unknown substitution model parameters. We demonstrate that this approximate gradient enables scaling of sampling-based inference, namely Bayesian inference via Hamiltonian Monte Carlo, under random-effects substitution models across large trees and state-spaces. Applied to a dataset of 583 SARS-CoV-2 sequences, an HKY model with random-effects shows strong signals of nonreversibility in the substitution process, and posterior predictive model checks clearly show that it is a more adequate model than a reversible model. When analyzing the pattern of phylogeographic spread of 1441 influenza A virus (H3N2) sequences between 14 regions, a random-effects phylogeographic substitution model infers that air travel volume adequately predicts almost all dispersal rates. A random-effects state-dependent substitution model reveals no evidence for an effect of arboreality on the swimming mode in the tree frog subfamily Hylinae. Simulations reveal that random-effects substitution models can accommodate both negligible and radical departures from the underlying base substitution model. We show that our gradient-based inference approach is over an order of magnitude more time efficient than conventional approaches. Copyright © 2023, The Authors. All rights reserved.

关键词： Phylogenetic

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Improved Prediction Of Ligand-Protein Binding Affinities By Meta-Modeling

arXiv

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arXiv 2023年

作者： Lee, Ho-Joon Emani, Prashant S. Gerstein, Mark B. Dept. of Genetics and Yale University New HavenCT06510 United States Yale Center for Genome Analysis Yale University New HavenCT06510 United States Dept. of Molecular Biophysics & Biochemistry Yale University New HavenCT06520 United States Program in Computational Biology & Bioinformatics Yale University New HavenCT06520 United States Dept. of Computer Science Yale University New HavenCT06520 United States Dept. of Statistics & Data Science Yale University New HavenCT06520 United States Dept. of Biomedical Informatics & Data Science Yale University New HavenCT06520 United States

The accurate screening of candidate drug ligands against target proteins through computational approaches is of prime interest to drug development efforts. Such virtual screening depends in part on methods to predict the binding affinity between ligands and proteins. Many computational models for binding affinity prediction have been developed, but with varying results across targets. Given that ensembling or meta-modeling approaches have shown great promise in reducing model-specific biases, we develop a framework to integrate published force-field-based empirical docking and sequence-based deep learning models. In building this framework, we evaluate many combinations of individual base models, training databases, and several meta-modeling approaches. We show that many of our meta-models significantly improve affinity predictions over base models. Our best meta-models achieve comparable performance to state-of-the-art deep learning tools exclusively based on 3D structures, while allowing for improved database scalability and flexibility through the explicit inclusion of features such as physicochemical properties or molecular descriptors. We further demonstrate improved generalization capability by our models using a large-scale benchmark of affinity prediction as well as a virtual screening application benchmark. Overall, we demonstrate that diverse modeling approaches can be ensembled together to gain meaningful improvement in binding affinity prediction. © 2023, CC BY-NC-SA.

关键词： Prediction models

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Deep inference of latent dynamics with spatio-temporal super-resolution using selective backpropagation through time 21

Deep inference of latent dynamics with spatio-temporal super...

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Proceedings of the 35th International Conference on Neural Information Processing Systems

作者： Feng Zhu Andrew R. Sedler Harrison A. Grier Nauman Ahad Mark A. Davenport Matthew T. Kaufman Andrea Giovannucci Chethan Pandarinath Neuroscience Graduate Program Emory University Center for Machine Learning Georgia Tech Computational Neuroscience Graduate Program The University of Chicago School of Electrical and Computer Engineering Georgia Tech Dept. of Organismal Biology and Anatomy The University of Chicago and Neuroscience Institute The University of Chicago Joint Dept. of Biomedical Engineering UNC Chapel Hill and NC State University and UNC Chapel Hill Neuroscience Center and NC State/UNC Closed-Loop Engineering for Advanced Rehabilitation (CLEAR) Coulter Dept. of Biomedical Engineering Emory University and Georgia Tech and Dept. of Neurosurgery Emory University

ISBN: (纸本)9781713845393

Modern neural interfaces allow access to the activity of up to a million neurons within brain circuits. However, bandwidth limits often create a trade-off between greater spatial sampling (more channels or pixels) and the temporal frequency of sampling. Here we demonstrate that it is possible to obtain spatio-temporal super-resolution in neuronal time series by exploiting relationships among neurons, embedded in latent low-dimensional population dynamics. Our novel neural network training strategy, selective backpropagation through time (SBTT), enables learning of deep generative models of latent dynamics from data in which the set of observed variables changes at each time step. The resulting models are able to infer activity for missing samples by combining observations with learned latent dynamics. We test SBTT applied to sequential autoencoders and demonstrate more efficient and higher-fidelity characterization of neural population dynamics in electrophysiological and calcium imaging data. In electrophysiology, SBTT enables accurate inference of neuronal population dynamics with lower interface bandwidths, providing an avenue to significant power savings for implanted neuroelectronic interfaces. In applications to two-photon calcium imaging, SBTT accurately uncovers high-frequency temporal structure underlying neural population activity, substantially outperforming the current state-of-the-art. Finally, we demonstrate that performance could be further improved by using limited, high-bandwidth sampling to pretrain dynamics models, and then using SBTT to adapt these models for sparsely-sampled data.

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An Open-Source Knowledge Graph Ecosystem for the Life Sciences

arXiv

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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

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Identification of evolutionarily stable functional and immunogenic sites across the SARS-CoV-2 proteome and the greater coronavirus family

Research Square

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Research Square 2020年 rs3rs-95030页

作者： Wang, Chen Konecki, Daniel M. Marciano, David C. Govindarajan, Harikumar Williams, Amanda M. Wastuwidyaningtyas, Brigitta Bourquard, Thomas Katsonis, Panagiotis Lichtarge, Olivier Baylor College of Medicine United States Department of Molecular and Human Genetics United States Quantitative and Computational Biosciences Graduate Program United States Cancer and Cell Biology Graduate Program Baylor College of Medicine HoustonTX77030 United States MAbSilico Nouzilly Centre France Computational and Integrative Biomedical Research Center Baylor College of Medicine HoustonTX77030 United States

Since the first recognized case of COVID-19, more than 100 million people have been infected worldwide. Global efforts in drug and vaccine development to fight the disease have yielded vaccines and drug candidates to cure COVID-19. However, the spread of SARS-CoV-2 variants threatens the continued efficacy of these treatments. In order to address this, we interrogate the evolutionary history of the entire SARS-CoV-2 proteome to identify evolutionarily conserved functional sites that can inform the search for treatments with broader coverage across the coronavirus family. Combining this information with the mutations observed in the current COVID-19 outbreak, we systematically and comprehensively define evolutionarily stable sites that may provide useful drug and vaccine targets and which are less likely to be compromised by the emergence of new virus strains. Several experimentally-validated effective drugs interact with these proposed target sites. In addition, the same evolutionary information can prioritize cross reactive antigens that are useful in directing multi-epitope vaccine strategies to illicit broadly neutralizing immune responses to the betacoronavirus family. Although the results are focused on SARS-CoV-2, these approaches stem from evolutionary principles that are agnostic to the organism or infective agent. © 2020, CC BY.

关键词： Coronavirus

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Developmental stage classification of Embryos using two-stream neural network with linear-chain conditional random field

arXiv

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arXiv 2021年

作者： Lukyanenko, Stanislav Jang, Won-Dong Wei, Donglai Struyven, Robbert Kim, Yoon Leahy, Brian Yang, Helen Rush, Alexander Ben-Yosef, Dalit Needleman, Daniel Pfister, Hanspeter Department of Informatics Technical University of Munich Germany School of Engineering and Applied Sciences Harvard University United States Department of Molecular and Cellular Biology Harvard University United States Graduate Program in Biophysics Harvard University United States University College London United Kingdom MIT United States Cornell University United States Center for Computational Biology Flatiron Institute United States Lis Maternity Hospital Tel-Aviv Sourasky Medical Center Israel Cell and Developmental Biology Tel-Aviv University Israel

The developmental process of embryos follows a monotonic order. An embryo can progressively cleave from one cell to multiple cells and finally transform to morula and blastocyst. For time-lapse videos of embryos, most existing developmental stage classification methods conduct per-frame predictions using an image frame at each time step. However, classification using only images suffers from overlapping between cells and imbalance between stages. Temporal information can be valuable in addressing this problem by capturing movements between neighboring frames. In this work, we propose a two-stream model for developmental stage classification. Unlike previous methods, our two-stream model accepts both temporal and image information. We develop a linear-chain conditional random field (CRF) on top of neural network features extracted from the temporal and image streams to make use of both modalities. The linear-chain CRF formulation enables tractable training of global sequential models over multiple frames while also making it possible to inject monotonic development order constraints into the learning process explicitly. We demonstrate our algorithm on two time-lapse embryo video datasets: i) mouse and ii) human embryo datasets. Our method achieves 98.1% and 80.6% for mouse and human embryo stage classification, respectively. Our approach will enable more profound clinical and biological studies and suggests a new direction for developmental stage classification by utilizing temporal information. Copyright © 2021, The Authors. All rights reserved.

关键词： Classification (of information)

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