BEGIN:VCALENDAR
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PRODID:-//Biomedical Mathematics Group - ECPv6.15.20//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:Biomedical Mathematics Group
X-ORIGINAL-URL:https://www.ibs.re.kr/bimag
X-WR-CALDESC:Events for Biomedical Mathematics Group
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:Asia/Seoul
BEGIN:STANDARD
TZOFFSETFROM:+0900
TZOFFSETTO:+0900
TZNAME:KST
DTSTART:20220101T000000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20231201T140000
DTEND;TZID=Asia/Seoul:20231201T160000
DTSTAMP:20260423T162151
CREATED:20231030T040908Z
LAST-MODIFIED:20231114T081702Z
UID:8665-1701439200-1701446400@www.ibs.re.kr
SUMMARY:Eui Min Jung\, Hard Limits and Performance Tradeoffs in a Class of Antithetic Integral Feedback Networks
DESCRIPTION:We will discuss about “Hard limits and performance tradeoffs in a class of antithetic integral feedback networks.” Cell systems 9.1 (2019): 49-63. \nAbstract \n\nFeedback regulation is pervasive in biology at both the organismal and cellular level. In this article\, we explore the properties of a particular biomolecular feedback mechanism called antithetic integral feedback\, which can be implemented using the binding of two molecules. Our work develops an analytic framework for understanding the hard limits\, performance tradeoffs\, and architectural properties of this simple model of biological feedback control. Using tools from control theory\, we show that there are simple parametric relationships that determine both the stability and the performance of these systems in terms of speed\, robustness\, steady-state error\, and leakiness. These findings yield a holistic understanding of the behavior of antithetic integral feedback and contribute to a more general theory of biological control systems.
URL:https://www.ibs.re.kr/bimag/event/2023-12-01-jc/
LOCATION:B378 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Journal Club
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20231124T140000
DTEND;TZID=Asia/Seoul:20231124T160000
DTSTAMP:20260423T162151
CREATED:20231030T040641Z
LAST-MODIFIED:20231114T081738Z
UID:8663-1700834400-1700841600@www.ibs.re.kr
SUMMARY:Dongju Lim\, An accurate probabilistic step finder for time-series analysis
DESCRIPTION:We will discuss about “An accurate probabilistic step finder for time-series analysis.” bioRxiv (2023): 2023-09. \nAbstract \n\n\n\n\nNoisy time-series data is commonly collected from sources including Förster Resonance Energy Transfer experiments\, patch clamp and force spectroscopy setups\, among many others. Two of the most common paradigms for the detection of discrete transitions in such time-series data include: hidden Markov models (HMMs) and step-finding algorithms. HMMs\, including their extensions to infinite state-spaces\, inherently assume in analysis that holding times in discrete states visited are geometrically–or\, loosely speaking in common language\, exponentially–distributed. Thus the determination of step locations\, especially in sparse and noisy data\, is biased by HMMs toward identifying steps resulting in geometric holding times. In contrast\, existing step-finding algorithms\, while free of this restraint\, often rely on ad hoc metrics to penalize steps recovered in time traces (by using various information criteria) and otherwise rely on approximate greedy algorithms to identify putative global optima. Here\, instead\, we devise a robust and general probabilistic (Bayesian) step-finding tool that neither relies on ad hoc metrics to penalize step numbers nor assumes geometric holding times in each state. As the number of steps themselves in a time-series are\, a priori unknown\, we treat these within a Bayesian nonparametric (BNP) paradigm. We find that the method developed\, Bayesian Nonparametric Step (BNP-Step)\, accurately determines the number and location of transitions between discrete states without any assumed kinetic model and learns the emission distribution characteristic of each state. In doing so\, we verify that BNP-Step can analyze sparser data sets containing higher noise and more closely-spaced states than otherwise resolved by current state-of-the-art methods. What is more\, BNP-Step rigorously propagates measurement uncertainty into uncertainty over state transition locations\, numbers\, and emission levels as characterized by the posterior. We demonstrate the performance of BNP-Step on both synthetic data as well as data drawn from force spectroscopy experiments. \n 
URL:https://www.ibs.re.kr/bimag/event/2023-11-24-jc/
LOCATION:B378 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Journal Club
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20231122T160000
DTEND;TZID=Asia/Seoul:20231122T170000
DTSTAMP:20260423T162151
CREATED:20230831T143538Z
LAST-MODIFIED:20240728T143214Z
UID:8405-1700668800-1700672400@www.ibs.re.kr
SUMMARY:Alfio Quarteroni\, Physics-based and data-driven numerical models for computational medicine
DESCRIPTION:Abstract: I will report on some recent results on modelling the heart\, the external circulation\, and their application to problems of clinical relevance. I will show that a proper integration between PDE-based and machine-learning algorithms can improve the computational efficiency and enhance the generality of our iHEART simulator.
URL:https://www.ibs.re.kr/bimag/event/alfio-quarteroni-physics-based-and-data-driven-numerical-models-for-computational-medicine/
LOCATION:ZOOM ID: 997 8258 4700 (Biomedical Mathematics Online Colloquium)\, (pw: 1234)
CATEGORIES:Biomedical Mathematics Online Colloquium
ATTACH;FMTTYPE=image/jpeg:https://www.ibs.re.kr/bimag/cms/wp-content/uploads/2023/08/Alfio-Quarteroni-e1722177125537.jpeg
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20231117T110000
DTEND;TZID=Asia/Seoul:20231117T120000
DTSTAMP:20260423T162151
CREATED:20230831T143713Z
LAST-MODIFIED:20240728T143844Z
UID:8408-1700218800-1700222400@www.ibs.re.kr
SUMMARY:Samuel Isaacson\, Spatial Particle Modeling of Immune Processes
DESCRIPTION:Abstract: \nSurface Plasmon Resonance (SPR) assays are a standard approach for quantifying kinetic parameters in antibody-antigen binding reactions. Classical SPR approaches ignore the bivalent structure of antibodies\, and use simplified ODE models to estimate effective reaction rates for such interactions. In this work we develop a new SPR protocol\, coupling a model that explicitly accounts for the bivalent nature of such interactions and the limited spatial distance over which such interactions can occur\, to a SPR assay that provides more features in the generated data. Our approach allows the estimation of bivalent binding kinetics and the spatial extent over which antibodies and antigens can interact\, while also providing substantially more robust fits to experimental data compared to classical ODE models. I will present our new modeling and parameter estimation approach\, and demonstrate how it is being used to study interactions between antibodies and spike protein. I will also explain how we make the overall parameter estimation problem computationally feasible via the construction of a surrogate approximation to the (computationally-expensive) particle model. The latter enables fitting of model parameters via standard optimization approaches. \nTime-permitting\, I will also give an introduction to our Catalyst.jl symbolic chemical reaction modeling library\, which we have recently demonstrated outperforms a number of popular systems biology simulation packages in solving ODE and stochastic reaction models. A distinguishing feature of Catalyst is the ease with which it integrates with other Julia libraries to enable sensitivity analysis\, parameter estimation studies\, structural identifiability analysis\, bifurcation analysis\, solution of the chemical master equation\, and a variety of higher-level functionality.
URL:https://www.ibs.re.kr/bimag/event/samuel-isaacson-spatial-particle-modeling-of-immune-processes/
LOCATION:ZOOM ID: 997 8258 4700 (Biomedical Mathematics Online Colloquium)\, (pw: 1234)
CATEGORIES:Biomedical Mathematics Online Colloquium
ATTACH;FMTTYPE=image/jpeg:https://www.ibs.re.kr/bimag/cms/wp-content/uploads/2023/08/Samuel-Isaacson-scaled-e1722177501809.jpeg
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20231110T140000
DTEND;TZID=Asia/Seoul:20231110T160000
DTSTAMP:20260423T162151
CREATED:20231030T040327Z
LAST-MODIFIED:20231109T000051Z
UID:8661-1699624800-1699632000@www.ibs.re.kr
SUMMARY:Seokjoo Chae\, Uncertainty quantified discovery of chemical reaction systems via Bayesian scientific machine learning
DESCRIPTION:We will discuss about “Uncertainty quantified discovery of chemical reaction systems via Bayesian scientific machine learning.” bioRxiv (2023): 2023-09. \n  \nAbstract \nThe recently proposed Chemical Reaction Neural Network (CRNN) discovers chemical reaction pathways from time resolved species concentration data in a deterministic manner. Since the weights and biases of a CRNN are physically interpretable\, the CRNN acts as a digital twin of a classical chemical reaction network. In this study\, we employ a Bayesian inference analysis coupled with neural ordinary differential equations (ODEs) on this digital twin to discover chemical reaction pathways in a probabilistic manner. This allows for estimation of the uncertainty surrounding the learned reaction network. To achieve this\, we propose an algorithm which combines neural ODEs with a preconditioned stochastic gradient langevin descent (pSGLD) Bayesian framework\, and ultimately performs posterior sampling on the neural network weights. We demonstrate the successful implementation of this algorithm on several reaction systems by not only recovering the chemical reaction pathways but also estimating the uncertainty in our predictions. We compare the results of the pSGLD with that of the standard SGLD and show that this optimizer more efficiently and accurately estimates the posterior of the reaction network parameters. Additionally\, we demonstrate how the embedding of scientific knowledge improves extrapolation accuracy by comparing results to purely data-driven machine learning methods. Together\, this provides a new framework for robust\, autonomous Bayesian inference on unknown or complex chemical and biological reaction systems. \n  \n 
URL:https://www.ibs.re.kr/bimag/event/2023-11-10-jc/
LOCATION:B378 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Journal Club
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20231110T110000
DTEND;TZID=Asia/Seoul:20231110T120000
DTSTAMP:20260423T162151
CREATED:20230831T142922Z
LAST-MODIFIED:20240728T144105Z
UID:8399-1699614000-1699617600@www.ibs.re.kr
SUMMARY:Matthew Simpson\, Efficient prediction\, estimation and identifiability analysis with mechanistic mathematical models
DESCRIPTION:Abstract: Interpreting data using mechanistic mathematical models provides a foundation for discovery and decision-making in all areas of science and engineering. Key steps in using mechanistic mathematical models to interpret data include: (i) identifiability analysis; (ii) parameter estimation; and (iii) model prediction. Here we present a systematic\, computationally efficient likelihood-based workflow that addresses all three steps in a unified way. Recently developed methods for constructing profile-wise prediction intervals enable this workflow and provide the central linkage between different workflow components. These methods propagate profile-likelihood-based confidence sets for model parameters to predictions in a way that isolates how different parameter combinations affect model predictions. We show how to extend these profile-wise prediction intervals to two-dimensional interest parameters\, and then combine profile-wise prediction confidence sets to give an overall prediction confidence set that approximates the full likelihood-based prediction confidence set well. We apply our methods to a range of synthetic data and real-world ecological data describing re-growth of coral reefs on the Great Barrier Reef after some external disturbance\, such as a tropical cyclone or coral bleaching event.
URL:https://www.ibs.re.kr/bimag/event/matthew-simpson-efficient-prediction-estimation-and-identifiability-analysis-with-mechanistic-mathematical-models/
LOCATION:ZOOM ID: 997 8258 4700 (Biomedical Mathematics Online Colloquium)\, (pw: 1234)
CATEGORIES:Biomedical Mathematics Online Colloquium
ATTACH;FMTTYPE=image/jpeg:https://www.ibs.re.kr/bimag/cms/wp-content/uploads/2023/08/Matthew-Simpson-e1722177652995.jpeg
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20231101T160000
DTEND;TZID=Asia/Seoul:20231101T170000
DTSTAMP:20260423T162151
CREATED:20230831T143129Z
LAST-MODIFIED:20240728T144218Z
UID:8402-1698854400-1698858000@www.ibs.re.kr
SUMMARY:Eder Zavala\, Quantitative analysis of high-resolution daily profiles of HPA axis hormones
DESCRIPTION:Abstract: The Hypothalamic-Pituitary-Adrenal (HPA) axis is the key regulatory pathway responsible for maintaining homeostasis under conditions of real or perceived stress. Endocrine responses to stressors are mediated by adrenocorticotrophic hormone (ACTH) and corticosteroid (CORT) hormones. In healthy\, non-stressed conditions\, ACTH and CORT exhibit highly correlated ultradian pulsatility with an amplitude modulated by circadian processes. Disruption of these hormonal rhythms can occur as a result of stressors or in the very early stages of disease. Despite the fact that misaligned endocrine rhythms are associated with increased morbidity\, a quantitative understanding of their mechanistic origin and pathogenicity is missing. Mathematically\, the HPA axis can be understood as a dynamical system that is optimised to respond and adapt to perturbations. Normally\, the body copes well with minor disruptions\, but finds it difficult to withstand severe\, repeated or long-lasting perturbations. Whilst a healthy HPA axis maintains a certain degree of robustness to stressors\, its fragility in diseased states is largely unknown\, and this understanding constitutes a critical step toward the development of digital tools to support clinical decision-making. This talk will explore how these challenges are being addressed by combining high-resolution biosampling techniques with mathematical and computational analysis methods. This interdisciplinary approach is helping us quantify the inter-individual variability of daily hormone profiles and develop novel “dynamic biomarkers” that serve as a normative reference and to signal endocrine dysfunction. By shifting from a qualitative to a quantitative description of the HPA axis\, these insights bring us a step closer to personalised clinical interventions for which timing is key.
URL:https://www.ibs.re.kr/bimag/event/eder-zavala-quantitative-analysis-of-high-resolution-daily-profiles-of-hpa-axis-hormones/
LOCATION:ZOOM ID: 997 8258 4700 (Biomedical Mathematics Online Colloquium)\, (pw: 1234)
CATEGORIES:Biomedical Mathematics Online Colloquium
ATTACH;FMTTYPE=image/jpeg:https://www.ibs.re.kr/bimag/cms/wp-content/uploads/2023/08/Eder-Zavala-e1722177727704.jpeg
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20231027T140000
DTEND;TZID=Asia/Seoul:20231027T160000
DTSTAMP:20260423T162151
CREATED:20230929T230744Z
LAST-MODIFIED:20231018T020236Z
UID:8566-1698415200-1698422400@www.ibs.re.kr
SUMMARY:Hyun Kim\, Significance analysis for clustering with single-cell RNA-sequencing data
DESCRIPTION:We will discuss about “Significance analysis for clustering with single-cell RNA-sequencing data”\, Grabski\, Isabella N.\, Kelly Street\, and Rafael A. Irizarry.\, Nature Methods (2023): 1-7. \nAbstract \n\n\n\nUnsupervised clustering of single-cell RNA-sequencing data enables the identification of distinct cell populations. However\, the most widely used clustering algorithms are heuristic and do not formally account for statistical uncertainty. We find that not addressing known sources of variability in a statistically rigorous manner can lead to overconfidence in the discovery of novel cell types. Here we extend a previous method\, significance of hierarchical clustering\, to propose a model-based hypothesis testing approach that incorporates significance analysis into the clustering algorithm and permits statistical evaluation of clusters as distinct cell populations. We also adapt this approach to permit statistical assessment on the clusters reported by any algorithm. Finally\, we extend these approaches to account for batch structure. We benchmarked our approach against popular clustering workflows\, demonstrating improved performance. To show practical utility\, we applied our approach to the Human Lung Cell Atlas and an atlas of the mouse cerebellar cortex\, identifying several cases of over-clustering and recapitulating experimentally validated cell type definitions.
URL:https://www.ibs.re.kr/bimag/event/2023-10-27-jc/
LOCATION:Daejeon
CATEGORIES:Journal Club
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20231020T140000
DTEND;TZID=Asia/Seoul:20231020T160000
DTSTAMP:20260423T162151
CREATED:20230929T231212Z
LAST-MODIFIED:20231018T020716Z
UID:8568-1697810400-1697817600@www.ibs.re.kr
SUMMARY:Hyeontae Jo\, AutoScore:A Machine Learning–Based Automatic Clinical Score Generator and Its Application to Mortality Prediction Using Electronic Health Records
DESCRIPTION:We will discuss about “AutoScore:A Machine Learning–Based Automatic Clinical Score Generator and Its Application to Mortality Prediction Using Electronic Health Records”\, Xie\, Feng\, et al.\, JMIR medical informatics 8.10 (2020): e21798. \nAbstract\nBackground: Risk scores can be useful in clinical risk stratification and accurate allocations of medical resources\, helping health providers improve patient care. Point-based scores are more understandable and explainable than other complex models and are now widely used in clinical decision making. However\, the development of the risk scoring model is nontrivial and has not yet been systematically presented\, with few studies investigating methods of clinical score generation using electronic health records. \nObjective: This study aims to propose AutoScore\, a machine learning-based automatic clinical score generator consisting of 6 modules for developing interpretable point-based scores. Future users can employ the AutoScore framework to create clinical scores effortlessly in various clinical applications. \nMethods: We proposed the AutoScore framework comprising 6 modules that included variable ranking\, variable transformation\, score derivation\, model selection\, score fine-tuning\, and model evaluation. To demonstrate the performance of AutoScore\, we used data from the Beth Israel Deaconess Medical Center to build a scoring model for mortality prediction and then compared the data with other baseline models using the receiver operating characteristic analysis. A software package in R 3.5.3 (R Foundation) was also developed to demonstrate the implementation of AutoScore. \nResults: Implemented on the data set with 44\,918 individual admission episodes of intensive care\, the AutoScore-created scoring models performed comparably well as other standard methods (ie\, logistic regression\, stepwise regression\, least absolute shrinkage and selection operator\, and random forest) in terms of predictive accuracy and model calibration but required fewer predictors and presented high interpretability and accessibility. The nine-variable\, AutoScore-created\, point-based scoring model achieved an area under the curve (AUC) of 0.780 (95% CI 0.764-0.798)\, whereas the model of logistic regression with 24 variables had an AUC of 0.778 (95% CI 0.760-0.795). Moreover\, the AutoScore framework also drives the clinical research continuum and automation with its integration of all necessary modules. \nConclusions: We developed an easy-to-use\, machine learning-based automatic clinical score generator\, AutoScore; systematically presented its structure; and demonstrated its superiority (predictive performance and interpretability) over other conventional methods using a benchmark database. AutoScore will emerge as a potential scoring tool in various medical applications.
URL:https://www.ibs.re.kr/bimag/event/2023-10-20-jc/
LOCATION:B378 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Journal Club
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20231020T110000
DTEND;TZID=Asia/Seoul:20231020T120000
DTSTAMP:20260423T162151
CREATED:20230831T143835Z
LAST-MODIFIED:20231124T001740Z
UID:8411-1697799600-1697803200@www.ibs.re.kr
SUMMARY:Tetsuya J. Kobayashi\, Optimality of Biological Information Processing
DESCRIPTION:Abstract: \nAlmost all biological systems possess the ability to gather environmental information and modulate their behaviors to adaptively respond to changing environments. While animals excel at sensing odors\, even simple bacteria can detect faint chemicals using stochastic receptors. They then navigate towards or away from the chemical source by processing this sensed information through intracellular reaction systems. \nIn the first half of our talk\, we demonstrate that the E. coli chemotactic system is optimally structured for sensing noisy signals and controlling taxis. We utilize filtering theory and optimal control theory to theoretically derive this optimal structure and compare it to the quantitatively verified biochemical model of chemotaxis. \nIn the latter half\, we discuss the limitations of traditional information theory\, filtering theory\, and optimal control theory in analyzing biological systems. Notably\, all biological systems\, especially simpler ones\, have constrained computational resources like memory size and energy\, which influence optimal behaviors. Conventional theories don’t directly address these resource constraints\, likely because they emerged during a period when computational resources were continually expanding. To address this gap\, we introduce the “memory-limited partially observable optimal control\,” a new theoretical framework developed by our group\, and explore its relevance to biological problems.
URL:https://www.ibs.re.kr/bimag/event/tetsuya-j-kobayashi-optimality-of-biological-information-processing/
LOCATION:ZOOM ID: 997 8258 4700 (Biomedical Mathematics Online Colloquium)\, (pw: 1234)
CATEGORIES:Biomedical Mathematics Online Colloquium
ATTACH;FMTTYPE=image/jpeg:https://www.ibs.re.kr/bimag/cms/wp-content/uploads/2023/08/Tetsuya-Kobayashi-1.jpeg
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20231006T140000
DTEND;TZID=Asia/Seoul:20231006T160000
DTSTAMP:20260423T162151
CREATED:20230929T225914Z
LAST-MODIFIED:20231005T021126Z
UID:8564-1696600800-1696608000@www.ibs.re.kr
SUMMARY:Olive Cawiding\, Power spectral estimate for discrete data
DESCRIPTION:We will discuss about “Power spectral estimate for discrete data”\, Nobert Marwan and Tobias Braun\, Chaos (2023). \n  \nAbstract \n\nThe identification of cycles in periodic signals is a ubiquitous problem in time series analysis. Many real-world datasets only record a signal as a series of discrete events or symbols. In some cases\, only a sequence of (non-equidistant) times can be assessed. Many of these signals are furthermore corrupted by noise and offer a limited number of samples\, e.g.\, cardiac signals\, astronomical light curves\, stock market data\, or extreme weather events. We propose a novel method that provides a power spectral estimate for discrete data. The edit distance is a distance measure that allows us to quantify similarities between non-equidistant event sequences of unequal lengths. However\, its potential to quantify the frequency content of discrete signals has so far remained unexplored. We define a measure of serial dependence based on the edit distance\, which can be transformed into a power spectral estimate (EDSPEC)\, analogous to the Wiener–Khinchin theorem for continuous signals. The proposed method is applied to a variety of discrete paradigmatic signals representing random\, correlated\, chaotic\, and periodic occurrences of events. It is effective at detecting periodic cycles even in the presence of noise and for short event series. Finally\, we apply the EDSPEC method to a novel catalog of European atmospheric rivers (ARs). ARs are narrow filaments of extensive water vapor transport in the lower troposphere and can cause hazardous extreme precipitation events. Using the EDSPEC method\, we conduct the first spectral analysis of European ARs\, uncovering seasonal and multi-annual cycles along different spatial domains. The proposed method opens new research avenues in studying of periodic discrete signals in complex real-world systems.
URL:https://www.ibs.re.kr/bimag/event/2023-10-06-jc/
LOCATION:B378 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Journal Club
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230926T160000
DTEND;TZID=Asia/Seoul:20230926T170000
DTSTAMP:20260423T162151
CREATED:20230924T061833Z
LAST-MODIFIED:20230924T061833Z
UID:8555-1695744000-1695747600@www.ibs.re.kr
SUMMARY:Jonathan Rubin\, Qualitative inverse problems: mapping from limited data to properties of dynamics and parameter values for ODE models
DESCRIPTION:
URL:https://www.ibs.re.kr/bimag/event/jonathan-rubin-qualitative-inverse-problems-mapping-from-limited-data-to-properties-of-dynamics-and-parameter-values-for-ode-models-2/
LOCATION:B378 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Biomedical Mathematics Seminar
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230922T140000
DTEND;TZID=Asia/Seoul:20230922T160000
DTSTAMP:20260423T162151
CREATED:20230901T091012Z
LAST-MODIFIED:20230906T083720Z
UID:8440-1695391200-1695398400@www.ibs.re.kr
SUMMARY:Yun Min Song\, A data-driven approach for timescale decomposition of biochemical reaction networks
DESCRIPTION:We will discuss about “A data-driven approach for timescale decomposition of biochemical reaction networks”\, Amir Akbari\, Zachary B. Haiman\, Bernhard O. Palsson\, bioRxiv (2023) \nAbstract \n\nUnderstanding the dynamics of biological systems in evolving environments is a challenge due to their scale and complexity. Here\, we present a computational framework for timescale decomposition of biochemical reaction networks to distill essential patterns from their intricate dynamics. This approach identifies timescale hierarchies\, concentration pools\, and coherent structures from time-series data\, providing a system-level description of reaction networks at physiologically important timescales. We apply this technique to kinetic models of hypothetical and biological pathways\, validating it by reproducing analytically characterized or previously known concentration pools of these pathways. Moreover\, by analyzing the timescale hierarchy of the glycolytic pathway\, we elucidate the connections between the stoichiometric and dissipative structures of reaction networks and the temporal organization of coherent structures. Specifically\, we show that glycolysis is a cofactor driven pathway\, the slowest dynamics of which are described by a balance between high-energy phosphate bond and redox trafficking. Overall\, this approach provides more biologically interpretable characterizations of network dynamics than large-scale kinetic models\, thus facilitating model reduction and personalized medicine applications. \n\n 
URL:https://www.ibs.re.kr/bimag/event/2023-09-22-jc/
LOCATION:B378 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Journal Club
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230920T160000
DTEND;TZID=Asia/Seoul:20230920T170000
DTSTAMP:20260423T162151
CREATED:20230831T142706Z
LAST-MODIFIED:20240728T144517Z
UID:8397-1695225600-1695229200@www.ibs.re.kr
SUMMARY:Sebastian Walcher\, Reaction networks: Reduction of dimension and critical parameters
DESCRIPTION:Abstract: Typically\, the mathematical description of reaction networks involves a system of parameter-dependent ordinary differential equations. Generally\, one is interested in the qualitative and quantitative behavior of solutions in various parameter regions. In applications\, identifying the reaction parameters is a fundamental task. Reduction of dimension is desirable from a practical perspective\, and even necessary when different timescales are present. For biochemical reaction networks\, a classical reduction technique assumes quasi-steady state (QSS) of certain species. From a general mathematical perspective\, singular perturbation theory – involving a small parameter – is often invoked. The talk is mathematically oriented. The following points will be discussed: Singular perturbation reduction in general coordinates. (“How does one compute reductions?”) Critical parameters for singular perturbations. (“How does one find small parameters?”) Quasi-steady state and singular perturbations. (“What is applicable\, what is correct?”)
URL:https://www.ibs.re.kr/bimag/event/sebastian-walcher-reaction-networks-reduction-of-dimension-and-critical-parameters/
LOCATION:ZOOM ID: 997 8258 4700 (Biomedical Mathematics Online Colloquium)\, (pw: 1234)
CATEGORIES:Biomedical Mathematics Online Colloquium
ATTACH;FMTTYPE=image/jpeg:https://www.ibs.re.kr/bimag/cms/wp-content/uploads/2023/08/Sebastian-Walcher-1-e1722177866528.jpeg
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230918T160000
DTEND;TZID=Asia/Seoul:20230918T170000
DTSTAMP:20260423T162151
CREATED:20230918T080118Z
LAST-MODIFIED:20230918T080118Z
UID:8524-1695052800-1695056400@www.ibs.re.kr
SUMMARY:Balazs Erdos\, Quantifying the dynamics of postmeal metabolism: Inference from challenge test data
DESCRIPTION:
URL:https://www.ibs.re.kr/bimag/event/balazs-erdos-quantifying-the-dynamics-of-postmeal-metabolism-inference-from-challenge-test-data/
LOCATION:B378 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Biomedical Mathematics Seminar
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230915T140000
DTEND;TZID=Asia/Seoul:20230915T160000
DTSTAMP:20260423T162151
CREATED:20230829T100538Z
LAST-MODIFIED:20230914T051626Z
UID:8371-1694786400-1694793600@www.ibs.re.kr
SUMMARY:Eui Min Jung\, Antithetic proportional-integral feedback for reduced variance and improved control performance of stochastic reaction networks
DESCRIPTION:We will discuss about “Antithetic proportional-integral feedback for reduced variance and improved control performance of stochastic reaction networks\n”\,Briat\, Corentin\, Ankit Gupta\, and Mustafa Khammash.\, Journal of The Royal Society Interface 15.143 (2018): 20180079 \nAbstract \n\n\n\n\n\n\n\nThe ability of a cell to regulate and adapt its internal state in response to unpredictable environmental changes is called homeostasis and this ability is crucial for the cell’s survival and proper functioning. Understanding how cells can achieve homeostasis\, despite the intrinsic noise or randomness in their dynamics\, is fundamentally important for both systems and synthetic biology. In this context\, a significant development is the proposed antithetic integral feedback (AIF) motif\, which is found in natural systems\, and is known to ensure robust perfect adaptation for the mean dynamics of a given molecular species involved in a complex stochastic biomolecular reaction network. From the standpoint of applications\, one drawback of this motif is that it often leads to an increased cell-to-cell heterogeneity or variance when compared to a constitutive (i.e. open-loop) control strategy. Our goal in this paper is to show that this performance deterioration can be countered by combining the AIF motif and a negative feedback strategy. Using a tailored moment closure method\, we derive approximate expressions for the stationary variance for the controlled network that demonstrate that increasing the strength of the negative feedback can indeed decrease the variance\, sometimes even below its constitutive level. Numerical results verify the accuracy of these results and we illustrate them by considering three biomolecular networks with two types of negative feedback strategies. Our computational analysis indicates that there is a trade-off between the speed of the settling-time of the mean trajectories and the stationary variance of the controlled species; i.e. smaller variance is associated with larger settling-time.
URL:https://www.ibs.re.kr/bimag/event/2023-09-15-jc/
LOCATION:B378 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Journal Club
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230914T160000
DTEND;TZID=Asia/Seoul:20230914T173000
DTSTAMP:20260423T162152
CREATED:20230913T040446Z
LAST-MODIFIED:20230913T040446Z
UID:8516-1694707200-1694712600@www.ibs.re.kr
SUMMARY:Jonathan Rubin\, Qualitative inverse problems: mapping from limited data to properties of dynamics and parameter values for ODE models
DESCRIPTION:
URL:https://www.ibs.re.kr/bimag/event/jonathan-rubin-qualitative-inverse-problems-mapping-from-limited-data-to-properties-of-dynamics-and-parameter-values-for-ode-models/
LOCATION:KAIST E6-1 1501 Auditorium\, 291 Daehak-ro\, Yuseong-gu\, Daejeon\, 34141\, Korea\, Republic of
CATEGORIES:Seminar
ATTACH;FMTTYPE=image/jpeg:https://www.ibs.re.kr/bimag/cms/wp-content/uploads/2023/09/2023FallMathColloquium-scaled.jpg
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230908T140000
DTEND;TZID=Asia/Seoul:20230908T160000
DTSTAMP:20260423T162152
CREATED:20230829T100233Z
LAST-MODIFIED:20230907T044351Z
UID:8369-1694181600-1694188800@www.ibs.re.kr
SUMMARY:Dongju Lim\, Exact solution of a three-stage model of stochastic gene expression including cell-cycle dynamics
DESCRIPTION:We will discuss about “Exact solution of a three-stage model of stochastic gene expression including cell-cycle dynamics”\, Wang\, Yiling\, et al.\, bioRxiv (2023): 2023-08. \n  \nAbstract \n\n\n\n\n\n\nThe classical three-stage model of stochastic gene expression predicts the statistics of single cell mRNA and protein number fluctuations as a function of the rates of promoter switching\, transcription\, translation\, degradation and dilution. While this model is easily simulated\, its analytical solution remains an unsolved problem. Here we modify this model to explicitly include cell-cycle dynamics and then derive an exact solution for the time-dependent joint distribution of mRNA and protein numbers. We show large differences between this model and the classical model which captures cell-cycle effects implicitly via effective first-order dilution reactions. In particular we find that the Fano factor of protein numbers calculated from a population snapshot measurement are underestimated by the classical model whereas the correlation between mRNA and protein can be either over- or underestimated\, depending on the timescales of mRNA degradation and promoter switching relative to the mean cell-cycle duration time. \n 
URL:https://www.ibs.re.kr/bimag/event/2023-09-08-jc/
LOCATION:B378 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Journal Club
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230906T160000
DTEND;TZID=Asia/Seoul:20230906T170000
DTSTAMP:20260423T162152
CREATED:20230904T132811Z
LAST-MODIFIED:20230904T132811Z
UID:8487-1694016000-1694019600@www.ibs.re.kr
SUMMARY:Jonathan Rubin\, Multiple timescale modeling for neural systems
DESCRIPTION:Abstract \nMathematical models of biological systems\, including neurons\, often feature components that evolve on very different timescales. Mathematical analysis of these multi-timescale systems can be greatly simplified by partitioning them into subsystems that evolve on different time scales. The subsystems are then analyzed semi-independently\, using a technique called fast-slow analysis. I will briefly describe the fast-slow analysis technique and its application to neuronal bursting oscillations and basic coupled neuron modeling. After this\, I will discuss fancier forms of dynamics such as canard oscillations\, mixed-mode oscillations\, and three-timescale dynamics. Although these examples all involve neural systems\, the methods can and have been applied to other biological\, chemical\, and physical systems.
URL:https://www.ibs.re.kr/bimag/event/jonathan-rubin-multiple-timescale-modeling-for-neural-systems/
LOCATION:B378 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Biomedical Mathematics Seminar
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230901T100000
DTEND;TZID=Asia/Seoul:20230901T120000
DTSTAMP:20260423T162152
CREATED:20230810T082738Z
LAST-MODIFIED:20230831T040832Z
UID:8236-1693562400-1693569600@www.ibs.re.kr
SUMMARY:Hyeongjun Jang\, Generalized Michaelis–Menten rate law with time-varying molecular concentrations
DESCRIPTION:We will discuss about “Generalized Michaelis–Menten rate law with time-varying molecular concentrations”\, Lim\, Roktaek\, et al.\,bioRxiv (2022): 2022-01 \n  \nAbstract \n\n\n\n\n\n\nThe Michaelis–Menten (MM) rate law has been the dominant paradigm of modeling biochemical rate processes for over a century with applications in biochemistry\, biophysics\, cell biology\, and chemical engineering. The MM rate law and its remedied form stand on the assumption that the concentration of the complex of interacting molecules\, at each moment\, approaches an equilibrium much faster than the molecular concentrations change. Yet\, this assumption is not always justified. Here\, we relax this quasi-steady state requirement and propose the generalized MM rate law for the interactions of molecules with active concentration changes over time. Our approach for time-varying molecular concentrations\, termed the effective time-delay scheme (ETS)\, is based on rigorously estimated time-delay effects in molecular complex formation. With particularly marked improvements in protein– protein and protein–DNA interaction modeling\, the ETS provides an analytical framework to interpret and predict rich transient or rhythmic dynamics (such as autogenously-regulated cellular adaptation and circadian protein turnover)\, which goes beyond the quasi-steady state assumption.
URL:https://www.ibs.re.kr/bimag/event/2023-09-01-jc/
LOCATION:B378 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Journal Club
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230814T120000
DTEND;TZID=Asia/Seoul:20230814T130000
DTSTAMP:20260423T162152
CREATED:20230730T231426Z
LAST-MODIFIED:20230814T093131Z
UID:8144-1692014400-1692018000@www.ibs.re.kr
SUMMARY:Dongju Lim and Olive Cawiding
DESCRIPTION:Dongju Lim: Mood Prediction for Bipolar Disorder Patient with Sleep Pattern Information \nOlive Cawiding: Detecting causality between weather variables and dengue cases in the Philippines \n  \n 
URL:https://www.ibs.re.kr/bimag/event/2023-08-14-lls/
LOCATION:Tea Room\, IBS\, Daejeon\, Daejeon\, 34141\, Korea\, Republic of
CATEGORIES:Lunch Lab Meeting Seminar
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230811T150000
DTEND;TZID=Asia/Seoul:20230811T170000
DTSTAMP:20260423T162152
CREATED:20230730T230909Z
LAST-MODIFIED:20230809T124859Z
UID:8141-1691766000-1691773200@www.ibs.re.kr
SUMMARY:Olive Cawiding\, Decomposing predictability to identify dominant causal drivers in complex ecosystems
DESCRIPTION:We will discuss about “ Decomposing predictability to identify dominant causal drivers in complex ecosystems ”\,Suzuki\, Kenta\, Shin-ichiro S. Matsuzaki\, and Hiroshi Masuya.\, Proceedings of the National Academy of Sciences 119.42 (2022): e2204405119. \n  \nAbstract \n\nEcosystems are complex systems of various physical\, biological\, and chemical processes. Since ecosystem dynamics are composed of a mixture of different levels of stochasticity and nonlinearity\, handling these data is a challenge for existing methods of time series–based causal inferences. Here\, we show that\, by harnessing contemporary machine learning approaches\, the concept of Granger causality can be effectively extended to the analysis of complex ecosystem time series and bridge the gap between dynamical and statistical approaches. The central idea is to use an ensemble of fast and highly predictive artificial neural networks to select a minimal set of variables that maximizes the prediction of a given variable. It enables decomposition of the relationship among variables through quantifying the contribution of an individual variable to the overall predictive performance. We show how our approach\, EcohNet\, can improve interaction network inference for a mesocosm experiment and simulated ecosystems. The application of the method to a long-term lake monitoring dataset yielded interpretable results on the drivers causing cyanobacteria blooms\, which is a serious threat to ecological integrity and ecosystem services. Since performance of EcohNet is enhanced by its predictive capabilities\, it also provides an optimized forecasting of overall components in ecosystems. EcohNet could be used to analyze complex and hybrid multivariate time series in many scientific areas not limited to ecosystems.
URL:https://www.ibs.re.kr/bimag/event/2023-08-11-jc/
LOCATION:B232 Seminar Room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Journal Club
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230804T140000
DTEND;TZID=Asia/Seoul:20230804T160000
DTSTAMP:20260423T162152
CREATED:20230729T064450Z
LAST-MODIFIED:20230730T231258Z
UID:8131-1691157600-1691164800@www.ibs.re.kr
SUMMARY:Seokhwan Moon\, The Internal Model Principle for Biomolecular Control Theory
DESCRIPTION:We will discuss about “ The Internal Model Principle for Biomolecular Control Theory ”\, Gupta\, Ankit\, and Mustafa Khammash.\, IEEE Open Journal of Control Systems 2 (2023): 63-69. \n  \nAbstract \nThe well-known Internal Model Principle (IMP) is a cornerstone of modern control theory. It stipulates the necessary conditions for asymptotic robustness of disturbance-prone dynamical systems by asserting that such a system must embed a subsystem in a feedback loop\, and this subsystem must be able to reduplicate the dynamic disturbance using only the regulated variable as the input. The insights provided by IMP can help in both designing suitable controllers and also in analysing the regulatory mechanisms in complex systems. So far the application of IMP in biology has been case-specific and ad hoc\, primarily due to the lack of generic versions of the IMP for biomolecular reaction networks that model biological processes. In this short article we highlight the need for an IMP in biology and discuss a recently developed version of it for biomolecular networks that exhibit maximal Robust Perfect Adaptation (maxRPA) by being robust to the maximum number of disturbance sources.
URL:https://www.ibs.re.kr/bimag/event/2023-08-04-jc/
LOCATION:B232 Seminar Room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Journal Club
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230731T120000
DTEND;TZID=Asia/Seoul:20230731T130000
DTSTAMP:20260423T162152
CREATED:20230629T055843Z
LAST-MODIFIED:20230731T143536Z
UID:7966-1690804800-1690808400@www.ibs.re.kr
SUMMARY:Yun Min Song and Seokjoo Chae
DESCRIPTION:Yun Min Song: Noisy delay denoises biochemical oscillators \nSeokjoo Chae: Reduction of spatiotemporal model and its validity condition
URL:https://www.ibs.re.kr/bimag/event/2023-07-31-lls/
LOCATION:Tea Room\, IBS\, Daejeon\, Daejeon\, 34141\, Korea\, Republic of
CATEGORIES:Lunch Lab Meeting Seminar
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230728T100000
DTEND;TZID=Asia/Seoul:20230728T110000
DTSTAMP:20260423T162152
CREATED:20230619T074840Z
LAST-MODIFIED:20230726T042649Z
UID:7948-1690538400-1690542000@www.ibs.re.kr
SUMMARY:Yun Min Song\, The singularity response reveals entrainment properties of the plant circadian clock
DESCRIPTION:We will discuss about “The singularity response reveals entrainment properties of the plant circadian clock”\, Masuda\, Kosaku\, et al.\, Nature Communications 12.1 (2021): 864. \nAbstract \n\n\n\n\n\n\nCircadian clocks allow organisms to synchronize their physiological processes to diurnal variations. A phase response curve allows researchers to understand clock entrainment by revealing how signals adjust clock genes differently according to the phase in which they are applied. Comprehensively investigating these curves is difficult\, however\, because of the cost of measuring them experimentally. Here we demonstrate that fundamental properties of the curve are recoverable from the singularity response\, which is easily measured by applying a single stimulus to a cellular network in a desynchronized state (i.e. singularity). We show that the singularity response of Arabidopsis to light/dark and temperature stimuli depends on the properties of the phase response curve for these stimuli. The measured singularity responses not only allow the curves to be precisely reconstructed but also reveal organ-specific properties of the plant circadian clock. The method is not only simple and accurate\, but also general and applicable to other coupled oscillator systems as long as the oscillators can be desynchronized. This simplified method may allow the entrainment properties of the circadian clock of both plants and other species in nature.
URL:https://www.ibs.re.kr/bimag/event/2023-07-28/
LOCATION:B232 Seminar Room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Journal Club
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230707T140000
DTEND;TZID=Asia/Seoul:20230707T160000
DTSTAMP:20260423T162152
CREATED:20230529T032440Z
LAST-MODIFIED:20230707T034944Z
UID:7807-1688738400-1688745600@www.ibs.re.kr
SUMMARY:Hyun Kim\, scPrisma infers\, filters and enhances topological signals in single-cell data using spectral template matching
DESCRIPTION:We will discuss about “scPrisma infers\, filters and enhances topological signals in single-cell data using spectral template matching”\, Karin\, Jonathan\, Yonathan Bornfeld\, and Mor Nitzan.\, Nature Biotechnology (2023): 1-10. \nAbstract \n\n\n\nSingle-cell RNA sequencing has been instrumental in uncovering cellular spatiotemporal context. This task is challenging as cells simultaneously encode multiple\, potentially cross-interfering\, biological signals. Here we propose scPrisma\, a spectral computational method that uses topological priors to decouple\, enhance and filter different classes of biological processes in single-cell data\, such as periodic and linear signals. We apply scPrisma to the analysis of the cell cycle in HeLa cells\, circadian rhythm and spatial zonation in liver lobules\, diurnal cycle in Chlamydomonas and circadian rhythm in the suprachiasmatic nucleus in the brain. scPrisma can be used to distinguish mixed cellular populations by specific characteristics such as cell type and uncover regulatory networks and cell–cell interactions specific to predefined biological signals\, such as the circadian rhythm. We show scPrisma’s flexibility in incorporating prior knowledge\, inference of topologically informative genes and generalization to additional diverse templates and systems. scPrisma can be used as a stand-alone workflow for signal analysis and as a prior step for downstream single-cell analysis.
URL:https://www.ibs.re.kr/bimag/event/2023-07-07-jc/
LOCATION:B232 Seminar Room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Journal Club
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230705T120000
DTEND;TZID=Asia/Seoul:20230705T130000
DTSTAMP:20260423T162152
CREATED:20230629T055533Z
LAST-MODIFIED:20230704T011831Z
UID:7964-1688558400-1688562000@www.ibs.re.kr
SUMMARY:Hyukpyo Hong and Seokmin Ha
DESCRIPTION:Hyukpyo Hong: Advancing Infectious Disease Modeling: Estimating Reproduction Number with Realistic Latent and Infectious Periods \nSeokmin Ha: Systematic inference-driven experiments reveal a fundamental mechanism governing clock protein interactions in plants
URL:https://www.ibs.re.kr/bimag/event/2023-07-05-lls/
LOCATION:Tea Room\, IBS\, Daejeon\, Daejeon\, 34141\, Korea\, Republic of
CATEGORIES:Lunch Lab Meeting Seminar
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230622T140000
DTEND;TZID=Asia/Seoul:20230622T160000
DTSTAMP:20260423T162152
CREATED:20230615T052932Z
LAST-MODIFIED:20230615T052932Z
UID:7932-1687442400-1687449600@www.ibs.re.kr
SUMMARY:Dae Wook kim\, "Wearable data science for personalized digital medicine"
DESCRIPTION:We will discuss about “Wearable data science for personalized digital medicine” \nAbstract \nMillions of people currently use wearables such as the Apple Watch to monitor their physical activity\, heart rate\, and other physiological signals\, generating an unprecedented amount of wearable data. This presents an opportunity for digital medicine to advance precision medicine. However\, the noisy nature of this wearable data makes it appear unusable without new mathematical techniques to extract key signals from it. In this talk\, I will discuss several techniques we have developed for analyzing this noisy time-series data\, including the level-set Kalman filter-based data assimilation technique – a new state space estimation method that can estimate the phase of circadian rhythms. Additionally\, I will introduce a Kalman filter-assisted autoencoder used for anomaly detection in time-series data\, as well as feature engineering based on persistent homology and mathematical modeling. These techniques have practical applications\, such as sleep scoring\, detection of physiological changes related to COVID-19\, and daily mood prediction.
URL:https://www.ibs.re.kr/bimag/event/2023-06-22-jc/
LOCATION:B378 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Journal Club
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230619T120000
DTEND;TZID=Asia/Seoul:20230619T130000
DTSTAMP:20260423T162152
CREATED:20230529T074802Z
LAST-MODIFIED:20230619T031311Z
UID:7837-1687176000-1687179600@www.ibs.re.kr
SUMMARY:Abbas Abbasli and Hyeongjun Jang
DESCRIPTION:Abbas Abbasli: Accurate prediction of in-vivo drug interaction mediated by cytochrome P450 inhibition \nHyeongjun Jang: Comparison of the inhibition constant approximation methods
URL:https://www.ibs.re.kr/bimag/event/2023-06-19-lls/
LOCATION:Tea Room\, IBS\, Daejeon\, Daejeon\, 34141\, Korea\, Republic of
CATEGORIES:Lunch Lab Meeting Seminar
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230612T120000
DTEND;TZID=Asia/Seoul:20230612T130000
DTSTAMP:20260423T162152
CREATED:20230529T074201Z
LAST-MODIFIED:20230529T110236Z
UID:7834-1686571200-1686574800@www.ibs.re.kr
SUMMARY:Hyun Kim
DESCRIPTION:TBD
URL:https://www.ibs.re.kr/bimag/event/2023-06-12-llb/
LOCATION:Tea Room\, IBS\, Daejeon\, Daejeon\, 34141\, Korea\, Republic of
CATEGORIES:Lunch Lab Meeting Seminar
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
END:VCALENDAR