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Annual International Conference of the IEEE Engineering in Medicine and biology Society (EMBC)

作者： Hongzhu Cui Dmitry Korkin Bioinformatics and Computational Biology Program Worcester Polytechnic Institute Worcester MA USA Department of Computer Science Worcester Polytechnic Institute Worcester MA USA

Study of genetic variants in the context of molecular networks has recently gained much attention. However, many of these studies suffer from the lack of functional information about the network rewiring effect of genetic variants. After large-scale homology modeling, plus extracting native structure from PDB database, we performed structure-based prediction about the rewiring effect using our SNP-IN tool, and it covers significantly more variants than experimental characterization. The analysis result confirms the widespread perturbations in human interactome and reveals the network rewiring behavior based on edge-based network robustness concept.

关键词： Proteins Diseases Robustness Genetics Databases bioinformatics

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Dynamic and static analysis of transcriptional regulatory networks in a hierarchical context

Dynamic and static analysis of transcriptional regulatory ne...

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IEEE International Workshop on Genomic Signal Processing and Statistics (GENSIPS)

作者： Nitin Bhardwaj Mark Gerstein Program in Computational Biology and Bioinformatics Yale University New Heaven CT USA Department of Computer Science Yale University New Heaven CT USA

Gene regulatory networks have been shown to share some common aspects with commonplace social governance structures such as hierarchies. Thus, we can get some intuition into their organization by arranging them into well-known hierarchical layouts. Here we study a wide range of regulatory networks (transcriptional, modification and phosphorylation) in a hierarchical context for five evolutionarily diverse species. We specify three levels of regulators - top, middle and bottom - which collectively regulate the non-regulator targets lying in the lowest fourth level, and we define quantities for nodes, levels and entire networks that measure their degree of collaboration and autocratic or democratic character. Overall we show that in all the networks studied, the middle level has the highest collaborative propensity and that co-regulatory partnerships occur most frequently amongst mid-level regulators, an observation that has parallels in efficient corporate settings where middle managers need to interact most to ensure organizational effectiveness. Then to study dynamic effects, superimpose the phenotypic effects of tampering with nodes and edges directly onto the hierarchies. We reconstruct modified hierarchies reflecting changes in the level of regulators within the hierarchy upon deletions or insertions of nodes or edges. Overall, we find that rewiring events that affect upper levels have a more dramatic effect on cell proliferation rate and survival than do those involving lower levels. We also investigate other features connected to the importance of upper-level regulators: expression divergence, back-up copies and expression level.

关键词： Regulators Collaboration Context bioinformatics Biochemistry Molecular biophysics Performance analysis

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Use of Bayesian networks to dissect the complexity of genetic disease: application to the Genetic Analysis Workshop 17 simulated data

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BMC proceedings 2011年第9-sup期5 Suppl 9卷 S37页

作者： Jia Kang Wei Zheng Lun Li Joon Sang Lee Xiting Yan Hongyu Zhao Interdepartmental Program in Computational Biology and Bioinformatics Yale University PO Box 208009 New Haven CT 06520-8114 USA. hongyu.zhao@yale.edu.

Complex diseases are often the downstream event of a number of risk factors, including both environmental and genetic variables. To better understand the mechanism of disease onset, it is of great interest to systematically investigate the crosstalk among various risk factors. Bayesian networks provide an intuitive graphical interface that captures not only the association but also the conditional independence and dependence structures among the variables, resulting in sparser relationships between risk factors and the disease phenotype than traditional correlation-based methods. In this paper, we apply a Bayesian network to dissect the complex regulatory relationships among disease traits and various risk factors for the Genetic Analysis Workshop 17 simulated data. We use the Bayesian network as a tool for the risk prediction of disease outcome.

关键词： Bayesian Network Disease Phenotype Area Under Curve Conditional Independence Risk Prediction Model

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Gene expression network analysis reveals pathway interactions of the IGF axis in breast cancer

Gene expression network analysis reveals pathway interaction...

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5th International Conference on bioinformatics and computational biology 2013, BICoB 2013

作者： Ramadan, Emad Perincheri, Sudhir Sprecher, Emmett Harris, Lyndsay Tuck, David Information and Computer Science Department King Fahd University Dhahran Saudi Arabia Department of Pathology Yale University New Haven United States Computational Biology and Bioinformatics Program Yale University New Haven United States Division of Hematology and Oncology Case Western Reserve University Cleveland United States

ISBN: (纸本)9781622769711

Background: Understanding crosstalk and feedback among oncogenic pathways is a critical challenge to overcoming resistance to targeted anticancer therapy. The topology of biological networks has increasingly been used to complement studies based on individual genes or gene collections. We apply network analysis to understand interactions among critical biological signaling pathways in breast cancer. Results: An overlapping clustering of the networks showed highly distinct patterns in patients with high IGF versus low IGF axis. We demonstrate through cluster comparison metrics and permutation studies that these differences are unlikely to occur by chance. IRS-1, an IGF adaptor protein, is shown to have a highly central place in the IGF high as compared to the IGF low networks. We further demonstrate that network connections reveal information about interactions of genes in TGF-beta, MAPK, and other pathways known to interact with IGF. Conclusions: Network analyses can provide novel insights and hypotheses about signaling pathways involved in feedback and crosstalk in breast cancer.

关键词： Crosstalk

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A Flow Artist for High-Dimensional Cellular Data 33

A Flow Artist for High-Dimensional Cellular Data

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33rd IEEE International Workshop on Machine Learning for Signal Processing, MLSP 2023

作者： MacDonald, Kincaid Bhaskar, Dhananjay Thampakkul, Guy Nguyen, Nhi Zhang, Joia Perlmutter, Michael Adelstein, Ian Krishnaswamy, Smita Yale University Department of Mathematics United States Pomona College Department of Mathematics United States University of Washington Department of Statistics United States Boise State University Department of Mathematics United States Yale University Department of Computer Science United States Yale University Applied Mathematics Program United States Yale University Computational Biology and Bioinformatics Program United States

ISBN: (纸本)9798350324112

We consider the problem of embedding point cloud data sampled from an underlying manifold with an associated flow or velocity. Such data arises in many contexts where static snapshots of dynamic entities are measured, including in high-throughput biology such as single-cell transcriptomics. Existing embedding techniques either do not utilize velocity information or embed the coordinates and velocities independently, i.e., they either impose velocities on top of an existing point embedding or embed points within a prescribed vector field. Here we present FlowArtist, a neural network that embeds points while jointly learning a vector field around the points. The combination allows FlowArtist to better separate and visualize velocity-informed structures. Our results, on toy datasets and single-cell RNA velocity data, illustrate the value of utilizing coordinate and velocity information in tandem for embedding and visualizing high-dimensional data. © 2023 IEEE.

关键词： RNA

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A linked data graph approach to integration of immunological data

A linked data graph approach to integration of immunological...

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IEEE International Conference on bioinformatics and Biomedicine

作者： Syed Ahmad Chan Bukhari Jeff Mandell Steven H. Kleinstein Kei-Hoi Cheung Division of Computer Science Mathematics and Science Lesley H. & William L. Collins College of Professional Studies St. John's University Interdepartmental Program in Computational Biology and Bioinformatics Yale University Department of Pathology Interdepartmental Program in Computational Biology and Bioinformatics Yale University Department of Emergency Medicine and Yale Center for Medical Informatics Computationa Biology and Bioinformaticcs Yale University

ISBN: (纸本)9781728118680

Systems biology involves the integration of multiple data types (across different data sources) to offer a more complete picture of the biological system being studied. While many existing biological databases are implemented using the traditional SQL (Structured Query Language) database technology, NoSQL database technologies have been explored as a more relationship-based, flexible and scalable method of data integration. In this paper, we describe how to use the Neo4J graph database to integrate a variety of types of data sets in the context of systems vaccinology. Specifically, we have converted into a common graph model diverse types of vaccine response measurement data from the NIH/NIAID ImmPort data repository, pathway data from Reactome, influenza virus strains from WHO, and taxonomic data from NCBI Taxon. While Neo4J provides a graph-based query language (Cypher) for data retrieval, we develop a web-based dashboard for users to easily browse and visualize data without the need to learn Cypher. In addition, we have prototyped a natural language query interface for users to interact with our system. In conclusion, we demonstrate the feasibility of using a graph-based database for storing and querying immunological data with complex biological relationships. Querying a graph database through such relationships has the potential to reveal novel relationships among heterogeneous biological data.

关键词： ontology knowledgebase graph database immunology influenza vaccine graphic library Knowledge Bases Influenza Vaccines Ontology Immunology data integration Passwords DNA Integration integration data types Data sources SQL

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Rewriting regulatory DNA to dissect and reprogram gene expression

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Cell 2025年

作者： Martyn, Gabriella E. Montgomery, Michael T. Jones, Hank Guo, Katherine Doughty, Benjamin R. Linder, Johannes Bisht, Deepa Xia, Fan Cai, Xiangmeng S. Chen, Ziwei Cochran, Kelly Lawrence, Kathryn A. Munson, Glen Pampari, Anusri Fulco, Charles P. Sahni, Nidhi Kelley, David R. Lander, Eric S. Kundaje, Anshul Engreitz, Jesse M. Department of Genetics Stanford University School of Medicine Stanford 94305 CA United States Basic Science and Engineering Initiative Stanford Children's Health Betty Irene Moore Children's Heart Center Stanford 94305 CA United States Calico Life Sciences LLC South San Francisco 94080 CA United States Department of Genitourinary Medical Oncology Division of Cancer Medicine The University of Texas MD Anderson Cancer Center Houston 77030 TX United States Department of Genomic Medicine The University of Texas MD Anderson Cancer Center Houston 77030 TX United States Department of Epigenetics and Molecular Carcinogenesis The University of Texas MD Anderson Cancer Center Houston 77230 TX United States Department of Bioengineering Stanford University Stanford 94305 CA United States Department of Computer Science Stanford University Stanford 94305 CA United States Novo Nordisk Foundation Center for Genomic Mechanisms of Disease Broad Institute of MIT and Harvard Cambridge 02142 MA United States Gene Regulation Observatory Broad Institute of MIT and Harvard Cambridge 02142 MA United States Broad Institute of MIT and Harvard Cambridge 02142 MA United States Department of Bioinformatics and Computational Biology The University of Texas MD Anderson Cancer Center Houston 77230 TX United States Quantitative and Computational Biosciences Program Baylor College of Medicine Houston 77030 TX United States Department of Biology MIT Cambridge 02139 MA United States Department of Systems Biology Harvard Medical School Boston 02115 MA United States Stanford Cardiovascular Institute Stanford University Stanford 94305 CA United States

Regulatory DNA provides a platform for transcription factor binding to encode cell-type-specific patterns of gene expression. However, the effects and programmability of regulatory DNA sequences remain difficult to map or predict. Here, we develop variant effects from flow-sorting experiments with CRISPR targeting screens (Variant-EFFECTS) to introduce hundreds of designed edits to endogenous regulatory DNA and quantify their effects on gene expression. We systematically dissect and reprogram 3 regulatory elements for 2 genes in 2 cell types. These data reveal endogenous binding sites with effects specific to genomic context, transcription factor motifs with cell-type-specific activities, and limitations of computational models for predicting the effect sizes of variants. We identify small edits that can tune gene expression over a large dynamic range, suggesting new possibilities for prime-editing-based therapeutics targeting regulatory DNA. Variant-EFFECTS provides a generalizable tool to dissect regulatory DNA and to identify genome editing reagents that tune gene expression in an endogenous context. © 2025 Elsevier Inc.

关键词： CRISPR enhancers gene regulation high-throughput screening non-coding variants predictive models prime editing RNA FlowFISH sequence design transcription factors

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Bayesian multinomial logistic normal models through marginally latent matrix-T processes

The Journal of Machine Learning Research

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The Journal of Machine Learning Research 2022年第1期23卷 255-296页

作者： Justin D. Silverman Kimberly Roche Zachary C. Holmes Lawrence A. David Sayan Mukherjee College of Information Science and Technology Department of Statistics and Institute for Computational and Data Science Penn State University University Park PA Program in Computational Biology and Bioinformatics Duke University Durham NC Department of Molecular Genetics and Microbiology Duke University Durham NC Department of Molecular Genetics and Microbiology and Center for Genomic and Computational Biology Duke University Durham NC Departments of Statistical Science Mathematics Computer Science Biostatistics & Bioinformatics Duke University Durham NC

Bayesian multinomial logistic-normal (MLN) models are popular for the analysis of sequence count data (e.g., microbiome or gene expression data) due to their ability to model multivariate count data with complex covariance structure. However, existing implementations of MLN models are limited to small datasets due to the non-conjugacy of the multinomial and logistic-normal distributions. Motivated by the need to develop efficient inference for Bayesian MLN models, we develop two key ideas. First, we develop the class of Marginally Latent Matrix-T Process (Marginally LTP) models. We demonstrate that many popular MLN models, including those with latent linear, non-linear, and dynamic linear structure are special cases of this class. Second, we develop an efficient inference scheme for Marginally LTP models with specific accelerations for the MLN subclass. Through application to MLN models, we demonstrate that our inference scheme are both highly accurate and often 4-5 orders of magnitude faster than MCMC.

关键词： Bayesian statistics multivariate analysis count data microbiome gene expression

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Hyperbolic Diffusion Procrustes Analysis for Intrinsic Representation of Hierarchical Data Sets

Hyperbolic Diffusion Procrustes Analysis for Intrinsic Repre...

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International Conference on Acoustics, Speech, and Signal Processing (ICASSP)

作者： Ya-Wei Eileen Lin Yuval Kluger Ronen Talmon Viterbi Faculty of Electrical and Computer Engineering Technion Interdepartmental Program in Computational Biology and Bioinformatics Yale University Applied Math Program Yale University Department of Pathology School of Medicine Yale University

In this paper, we present Hyperbolic Diffusion Procrustes Analysis (HDPA), a new method for informative representation of hierarchical datasets based on hyperbolic geometry, diffusion geometry, and Procrustes analysis. Our method jointly embeds multiple datasets in a product manifold of hyperbolic spaces, where the data's hidden common hierarchical structure is provably recovered. In addition, our method generates an intrinsic embedding that accommodates the joint representation of multiple datasets with different features, acquired by different equipment, at different sites, or under different environmental conditions. Experimental results demonstrate the efficacy of HDPA on three biomedical datasets comprising heterogeneous gene expression and mass cytometry data.

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Association between response to brief trastuzumab exposure in cell lines and early stage HER2+ breast tumors 11

Association between response to brief trastuzumab exposure i...

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2011 ACM Conference on bioinformatics, computational biology and Biomedicine, ACM-BCB 2011

作者： Sprecher, Emmett Sarkar, Sudipa Kleinstein, Steven H. Narayan, Murli Winer, Eric Tuck, David Lezon-Geyda, Kimberly Krop, Ian Harris, Lyndsay Department of Pathology Pathology Informatics United States Interdepartmental Program in Computational Biology and Bioinformatics United States Medical Oncology Yale Cancer Center United States School of Medicine Yale University New Haven CT United States Department of Medical Oncology Dana-Farber Cancer Institute Boston MA United States

ISBN: (纸本)9781450307963

Human epidermal growth factor receptor 2 amplified (HER2+) breast cancer is common and aggressive. Trastuzumab is a targeted therapy to the HER2 cell surface receptor and has greatly improved prognosis for HER2+ breast cancer patients, but trastuzumab-resistance is a significant problem. Few biomarkers of trastuzumab resistance of response have been found, and there has been tremendous difficulty identifying in vitro biomarkers that transfer to the in vivo HER2+ breast cancer setting. We identified gene expression signatures of trastuzumabresponse and trastuzumab-resistance in HER2+ breast cancer cell lines across 24-hour exposure to trastuzumab. A set of 180-genes changed significantly in a trastuzumab-sensitive HER2+ cell line (BT474) and 58 genes changed significantly across treatment in a trastuzumab-resistant HER2+ cell line (UACC812). To demonstrate that these signatures have clinical relevance, we applied them in vivo to gene expression profiles from early stage HER2+ breast tumors treated with a single dose of trastuzumab. We found that the BT474 trastuzumabresponsive signature was enriched among the changes in expression across treatment for responsive patients. The expression change for the BT474 signature genes was also able to partially cluster responsive and resistant breast tumors by outcome. A subset of the UACC812 trastuzumab-resistance signature was also enriched in the differential between responsive and resistant tumors prior to trastuzumab treatment. These results show for the first time that cell line-derived gene signatures can be useful in identifying whether breast cancer patients will ultimately benefit from trastuzumab treatment. This approach might one day be applied to enhance clinical treatment decisions. Copyright © 2011 ACM.

关键词： Gene expression

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