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Leveraging Generative Artificial Intelligence in Diagnosis of Thrombotic Microangiopathies: Focus on Thrombotic Thrombocytopenic Purpura

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Blood 2024年 144卷 2616-2616页

作者： Eunhee Choi Jung-Hyun Lee Robert McDougal William W Lytton Lincoln Medical & Mental Health Center New York NY Department of Neurology State University of New York Downstate Health Sciences University New York NY Program in Computational Biology and Bioinformatics Yale University New haven CT

Introduction Thrombotic microangiopathies (TMA), with etiologies ranging from benign to life-threatening, necessitates rapid and accurate diagnosis, particularly for thrombotic thrombocytopenic purpura (TTP), to initiate timely plasmapheresis preventing severe outcomes. Diagnosing TTP is challenging due to overlapping clinical features with other causes of TMA, such as disseminated intravascular coagulation (DIC), immune thrombocytopenic purpura (ITP), and atypical hemolytic uremic syndrome (aHUS), compounded by that specific diagnostic tests such as biopsies or ADAMTS13 activity assays do not result immediately. This study explored GPT-4's capability in suggesting differential diagnoses for TMA patients and identifying a provisional diagnosis of TTP based on clinical presentation and basic diagnostic workup to determine the need for prompt plasmapheresis, assessing its potential as a diagnostic support tool. Method We utilized open-access case reports from PubMed Central that provided a comprehensive list of cases with diagnosis of TMA. The exclusion criteria included cases with no access, copyright permission issues, preprints, insufficient description, non-case reports, non-English language, and no established diagnosis for TMA. Each case input including only the history and physical examination (H&P) and basic diagnostic workup excluding the confirmatory diagnosis was presented to GPT-4 in three separate trials and was prompted to provide clinical reasoning that both favored or rejected the diagnosis of TTP, create a top three differential diagnoses list selected from a comprehensive list of TMA diagnoses, and determine the necessity of plasmapheresis. Generated results were subsequently compared with the confirmed case diagnosis and management provided within the case report. Result An initial PubMed Central search identified 424 cases; 326 were excluded, resulting in 98 eligible cases. The top three differential diagnoses generated for each case in all three t

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ζ-QVAE: A Quantum Variational Autoencoder utilizing Regularized Mixed-state Latent Representations

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arXiv 2024年

作者： Wang, Gaoyuan Warrell, Jonathan Emani, Prashant S. Gerstein, Mark Program in Computational Biology and Bioinformatics Yale University New HavenCT06520 United States Department of Molecular Biophysics and Biochemistry Yale University New HavenCT06520 United States Department of Computer Science Yale University New HavenCT06520 United States Department of Statistics & Data Science Yale University New HavenCT06520 United States Department of Biomedical Informatics & Data Science Yale University New HavenCT06520 United States NEC Laboratories America PrincetonNJ08540 United States

A major challenge in near-term quantum computing is its application to large real-world datasets due to scarce quantum hardware resources. One approach to enabling tractable quantum models for such datasets involves compressing the original data to manageable dimensions while still representing essential information for downstream analysis. In classical machine learning, variational autoencoders (VAEs) facilitate efficient data compression, representation learning for subsequent tasks, and novel data generation. However, no model has been proposed that exactly captures all of these features for direct application to quantum data on quantum computers. Some existing quantum models for data compression lack regularization of latent representations, thus preventing direct use for generation and control of generalization. Others are hybrid models with only some internal quantum components, impeding direct training on quantum data. To bridge this gap, we present a fully quantum framework, ζ-QVAE, which encompasses all the capabilities of classical VAEs and can be directly applied for both classical and quantum data compression. Our model utilizes regularized mixed states to attain optimal latent representations. It accommodates various divergences for reconstruction and regularization. Furthermore, by accommodating mixed states at every stage, it can utilize the full-data density matrix and allow for a"global"training objective. Doing so, in turn, makes efficient optimization possible and has potential implications for private and federated learning. In addition to exploring the theoretical properties of ζ-QVAE, we demonstrate its performance on representative genomics and synthetic data. Our results consistently indicate that ζ-QVAE exhibits similar or better performance compared to matched classical models. © 2024, CC BY-NC-ND.

关键词： Large datasets

Cell2Sentence: Teaching Large Language Models the Language of biology 41

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Cell2Sentence: Teaching Large Language Models the Language o...

41st International Conference on Machine Learning, ICML 2024

作者： Levine, Daniel Rizvi, Syed Asad Lévy, Sacha Pallikkavaliyaveetil, Nazreen Zhang, David Chen, Xingyu Ghadermarzi, Sina Wu, Ruiming Zheng, Zihe Vrkic, Ivan Zhong, Anna Raskin, Daphne Han, Insu de Oliveira Fonseca, Antonio Henrique Caro, Josue Ortega Karbasi, Amin Dhodapkar, Rahul M. van Dijk, David Department of Computer Science Yale University New HavenCT United States School of Engineering Applied Science University of Pennsylvania PhiladelphiaPA United States School of Computer and Communication Sciences Swiss Federal Institute of Technology Lausanne Lausanne Switzerland Department of Neuroscience Yale School of Medicine New HavenCT United States Wu Tsai Institute Yale University New HavenCT United States Google United States Yale Institute for Foundations of Data Science New HavenCT United States Yale School of Engineering and Applied Science New HavenCT United States Roski Eye Institute University of Southern California Los AngelesCA United States Yale School of Medicine New HavenCT United States Cardiovascular Research Center Yale School of Medicine New HavenCT United States Interdepartmental Program in Computational Biology & Bioinformatics Yale University New HavenCT United States

We introduce Cell2Sentence (C2S), a novel method to directly adapt large language models to a biological context, specifically single-cell transcriptomics. By transforming gene expression data into"cell sentences," C2S bridges the gap between natural language processing and biology. We demonstrate cell sentences enable the finetuning of language models for diverse tasks in biology, including cell generation, complex cell-type annotation, and direct data-driven text generation. Our experiments reveal that GPT-2, when fine-tuned with C2S, can generate biologically valid cells based on cell type inputs, and accurately predict cell types from cell sentences. This illustrates that language models, through C2S finetuning, can acquire a significant understanding of single-cell biology while maintaining robust text generation capabilities. C2S offers a flexible, accessible framework to integrate natural language processing with transcriptomics, utilizing existing models and libraries for a wide range of biological applications. Copyright 2024 by the author(s)

关键词： Gene expression

Author Correction: Single-cell multi-ome regression models identify functional and disease-associated enhancers and enable chromatin potential analysis

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Nature genetics 2024年第6期56卷 1319页

作者： Sneha Mitra Rohan Malik Wilfred Wong Afsana Rahman Alexander J Hartemink Yuri Pritykin Kushal K Dey Christina S Leslie Computational and Systems Biology Program Memorial Sloan Kettering Cancer Center New York City NY USA. Rye Country Day School Rye NY USA. Tri-Institutional Training Program in Computational Biology and Medicine New York City NY USA. Hunter College City University of New York New York City NY USA. Department of Computer Science Duke University Durham NC USA. Program in Computational Biology and Bioinformatics Duke University Durham NC USA. Center for Genomic and Computational Biology Duke University Durham NC USA. Department of Computer Science Princeton University Princeton NJ USA. Lewis-Sigler Institute for Integrative Genomics Princeton University Princeton NJ USA. Computational and Systems Biology Program Memorial Sloan Kettering Cancer Center New York City NY USA. deyk@***. Computational and Systems Biology Program Memorial Sloan Kettering Cancer Center New York City NY USA. lesliec@***.

Characterizing the mechanical response of metallic glasses to uniaxial tension using a spring network model

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arXiv 2023年

作者： Nawano, Aya Schroers, Jan Shattuck, Mark D. O’Hern, Corey S. Department of Mechanical Engineering and Materials Science Yale University New HavenCT06520 United States Benjamin Levich Institute and Physics Department The City College of New York New YorkNY10031 United States Department of Physics Yale University New HavenCT06520 United States Department of Applied Physics Yale University New HavenCT06520 United States Graduate Program in Computational Biology and Bioinformatics Yale University New HavenCT06520 United States

Metallic glasses are frequently used as structural materials. Therefore, it is important to develop methods to predict their mechanical response as a function of the microstructure prior to loading. We develop a novel coarse-grained spring network model, which describes the mechanical response of metallic glasses using an equivalent series network of springs, which can break and re-form to mimic atomic rearrangements during deformation. To validate the spring network model, we perform numerical simulations of quasistatic, uniaxial tensile deformation of Lennard-Jones and embedded atom method (EAM) potentials for Cu50Zr50 metallic glasses in the absence of large-scale shear band formation. We consider samples prepared using a wide range of cooling rates and with different amounts of crystalline order. We show that both the Lennard-Jones and EAM models possess qualitatively similar stress σ versus strain γ curves. By specifying five parameters in the spring network model (ultimate strength, strain at ultimate strength, slopes of σ(γ) at γ = 0 and at large strain, and strain at fracture where σ = 0), we can accurately describe the form of the stress-strain curves during uniaxial tension for the computational studies of Cu50Zr50, as well as recent experimental studies of several Zr-based metallic glasses. For the computational studies of Cu50Zr50, we find that the yield strain distribution is shifted to larger strains for slowly cooled glasses compared to rapidly cooled glasses. In addition, the average number of new springs and their rate of formation decreases with decreasing cooling rate. These effects offset each other at large strains, causing the stress-strain curve to become independent of the sample preparation protocol in this regime. In future studies, we will extract the parameters that define the spring network model directly from atomic rearrangements that occur during uniaxial deformation. © 2023, CC BY-NC-ND.

关键词： Metallic glass

Integrative modeling of transmitted and de novo variants identifies novel risk genes for congenital heart disease

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Quantitative biology 2021年第2期9卷 216-227页

作者： Mo Li Xue Zeng Chentian Jin Sheng Chih Jin Weilai Dong Martina Brueckner Richard Lifton Qiongshi Lu Hongyu Zhao Department of Biostatistics Yale School of Public HealthNew HavenCT 06510USA Department of Genetics Yale UniversityNew HavenCT 06510USA Department of Molecular Cellular&Developmental BiologyYale UniversityCT 06510USA Department of Genetics Washington University School of MedicineSt LouisMO 63110USA Department of Pediatrics Yale UniversityNew HavenCT 06510USA Laboratory of Human Genetics and Genomics Rockefeller UniversityNew YorkNY 10065USA Department of Biostatistics and Medical Informatics University of Wisconsin-MadisonMadisonWl 53792USA Program of Computational Biology and Bioinformatics Yale UniversityNew HavenCT 06510USA

Background:Whole-exome sequencing(WES)studies have identified multiple genes enriched for de novo mutations(DNMs)in congenital heart disease(CHD)***,risk gene identification based on DNMs alone remains statistically challenging due to heterogenous etiology of CHD and low mutation rate in each ***:In this manuscript,we introduce a hierarchical Bayesian framework for gene-level association test which jointly analyzes de novo and rare transmitted *** integrative modeling of multiple types of genetic variants,gene-level annotations,and reference data from large population cohorts,our method accurately characterizes the expected frequencies of both de novo and transmitted variants and shows improved statistical power compared to analyses based on DNMs ***:Applied to WES data of 2,645 CHD proband-parent trios,our method identified 15 significant genes,half of which are novel,leading to new insights into the genetic bases of ***:These results showcase the power of integrative analysis of transmitted and de novo variants for disease gene discovery.

关键词： rare variants gene-level association test congenital heart disease de novo mutation

AI solutions for drafting in Magic: The gathering

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arXiv 2020年

作者： Ward, Henry N. Brooks, Daniel J. Troha, Dan Mills, Bobby Khakhalin, Arseny S. Bioinformatics and Computational Biology Graduate Program University of Minnesota MinneapolisMN United States *** San DiegoCA United States Biology Program Bard College Annandale-on-HudsonNY United States

Drafting in Magic the Gathering is a sub-game within a larger trading card game, where several players progressively build decks by picking cards from a common pool. Drafting poses an interesting problem for game and AI research due to its large search space, mechanical complexity, multiplayer nature, and hidden information. Despite this, drafting remains understudied, in part due to a lack of high-quality, public datasets. To rectify this problem, we present a dataset of over 100,000 simulated, anonymized human drafts collected from ***. We also propose four diverse strategies for drafting agents, including a primitive heuristic agent, an expert-tuned complex heuristic agent, a Naive Bayes agent, and a deep neural network agent. We benchmark their ability to emulate human drafting, and show that the deep neural network agent outperforms other agents, while the Naive Bayes and expert-tuned agents outperform simple heuristics. We analyze the accuracy of AI agents across the timeline of a draft, and describe unique strengths and weaknesses for each approach. This work helps to identify next steps in the creation of humanlike drafting agents, and can serve as a benchmark for the next generation of drafting bots. Copyright © 2020, The Authors. All rights reserved.

关键词： Deep neural networks

Variational methods for Learning Multilevel Genetic Algorithms using the Kantorovich Monad

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arXiv 2024年

作者： Warrell, Jonathan Alesiani, Francesco Smith, Cameron Mösch, Anja Min, Martin Renqiang NEC Laboratories America Machine Learning Department PrincetonNJ08540 United States Department of Molecular Biophysics and Biochemistry Yale University New HavenCT06520 United States Program in Computational Biology and Bioinformatics Yale University New HavenCT06520 United States NEC Laboratories Europe Kurfuerstenanlage 36 HeidelbergD-69115 Germany Molecular Pathology Unit Center for Cancer Research Massachusetts General Hospital Research Institute Department of Pathology Harvard Medical School BostonMA United States Broad Institute of MIT and Harvard CambridgeMA United States

Levels of selection and multilevel evolutionary processes are essential concepts in evolutionary theory, and yet there is a lack of common mathematical models for these core ideas. Here, we propose a unified mathematical framework for formulating and optimizing multilevel evolutionary processes and genetic algorithms over arbitrarily many levels based on concepts from category theory and population genetics. We formulate a multilevel version of the Wright-Fisher process using this approach, and we show that this model can be analyzed to clarify key features of multilevel selection. Particularly, we derive an extended multilevel probabilistic version of Price's Equation via the Kantorovich Monad, and we use this to characterize regimes of parameter space within which selection acts antagonistically or cooperatively across levels. Finally, we show how our framework can provide a unified setting for learning genetic algorithms (GAs), and we show how we can use a Variational Optimization and a multi-level analogue of coalescent analysis to fit multilevel GAs to simulated data. Copyright © 2024, The Authors. All rights reserved.

关键词： Genetic algorithms

Communicationmachine Learning-Based QSAR and LB-PaCS-MD Guided Design of SARs-CoV-2 Main Protease Inhibitors

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SSRN

SSRN 2024年

作者： Toopradab, Borwornlak Xie, Wanting Duan, Lian Hengphasatporn, Kowit Harada, Ryuhei Sinsulpsiri, Silpsiri Shigeta, Yasuteru Shi, Liyi Maitarad, Phornphimon Rungrotmongkol, Thanyada Program in Bioinformatics and Computational Biology Graduate School Chulalongkorn University Bangkok10330 Thailand Center of Excellence in Biocatalyst and Sustainable Biotechnology Department of Biochemistry Faculty of Science Chulalongkorn University Bangkok10330 Thailand Research Center of Nano Science and Technology Department of Chemistry College of Science Shanghai University Shanghai200444 China University of Tsukuba 1-1-1 Tennodai Ibaraki Tsukuba305-8577 Japan Graduate School of Pure and Applied Sciences University of Tsukuba 1-1-1 Tennodai Ibaraki305–8571 Japan Emerging Industries Institute Shanghai University Zhejiang Jiaxing314006 China

The global outbreak of the COVID-19 pandemic caused by the SARS-CoV-2 virus had led to profound respiratory health implications. This study focused on designing organoselenium-based inhibitors targeting the SARS-CoV-2 main protease (Mpro). The ligand-binding pathway sampling method based on parallel cascade selection molecular dynamics (LB-PaCS-MD) simulations was employed to elucidate plausible paths and conformations of ebselen, a synthetic organoselenium drug, within the Mpro catalytic site. Ebselen effectively engaged the active site, adopting proximity to H41 and interacting through the benzoisoselenazole ring in a π-π T-shaped arrangement, with an additional π-sulfur interaction with C145. In addition, the ligand-based drug design using the QSAR with GFA-MLR, RF, and ANN models were employed for biological activity prediction. The QSAR-ANN model showed robust statistical performance, with an R2training exceeding 0.98 and an RMSEtest of 0.21, indicating its suitability for predicting biological activities. Integration the ANN model with the LB-PaCS-MD insights enabled the rational design of novel compounds anchored in the ebselen core structure, identifying promising candidates with favorable predicted IC50 values. The designed compounds exhibited suitable drug-like characteristics and adopted an active conformation similar to ebselen, inhibiting Mpro function. These findings represent a synergistic approach merging ligand and structure-based drug design;with the potential to guide experimental synthesis and enzyme assay testing. © 2024, The Authors. All rights reserved.

关键词： Coronavirus