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:20230602T140000
DTEND;TZID=Asia/Seoul:20230602T160000
DTSTAMP:20260425T235747
CREATED:20230529T032114Z
LAST-MODIFIED:20230529T032114Z
UID:7803-1685714400-1685721600@www.ibs.re.kr
SUMMARY:Eui Min Jung\, Uncovering specific mechanisms across cell types in dynamical models
DESCRIPTION:We will discuss about “Uncovering specific mechanisms across cell types in dynamical models”\, Hauber\, Adrian Lukas\, Marcus Rosenblatt\, and Jens Timmer.\, bioRxiv (2023): 2023-01. \nAbstract \nOrdinary differential equations are frequently employed for mathematical modeling of biological systems. The identification of mechanisms that are specific to certain cell types is crucial for building useful models and to gain insights into the underlying biological processes. Regularization techniques have been proposed and applied to identify mechanisms specific to two cell types\, e.g.\, healthy and cancer cells\, including the LASSO (least absolute shrinkage and selection operator). However\, when analyzing more than two cell types\, these approaches are not consistent\, and require the selection of a reference cell type\, which can affect the results. \nTo make the regularization approach applicable to identifying cell-type specific mechanisms in any number of cell types\, we propose to incorporate the clustered LASSO into the framework of ordinary differential equation modeling by penalizing the pairwise differences of the logarithmized fold-change parameters encoding a specific mechanism in different cell types. The symmetry introduced by this approach renders the results independent of the reference cell type. We discuss the necessary adaptations of state-of-the-art numerical optimization techniques and the process of model selection for this method. We assess the performance with realistic biological models and synthetic data\, and demonstrate that it outperforms existing approaches. Finally\, we also exemplify its application to published biological models including experimental data\, and link the results to independent biological measurements.
URL:https://www.ibs.re.kr/bimag/event/2023-06-02-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:20230608T110000
DTEND;TZID=Asia/Seoul:20230608T120000
DTSTAMP:20260425T235747
CREATED:20230601T080809Z
LAST-MODIFIED:20230605T043518Z
UID:7870-1686222000-1686225600@www.ibs.re.kr
SUMMARY:Seonjin Kim\, Nonparametric vs Parametric Regression
DESCRIPTION:To understand nonparametric regression\, we should know first what the parametric model is. Simply speaking\, the parametric regression model consists of many assumptions and the nonparametric regression model eases the assumptions. I will introduce what assumptions the parametric regression model has and how the nonparametric regression model relieves them. In addition\, their pros and cons will be also presented.
URL:https://www.ibs.re.kr/bimag/event/nonparametric-vs-parametric-regression/
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:20230609T110000
DTEND;TZID=Asia/Seoul:20230609T120000
DTSTAMP:20260425T235747
CREATED:20230218T033305Z
LAST-MODIFIED:20230529T011204Z
UID:7356-1686308400-1686312000@www.ibs.re.kr
SUMMARY:Sushmita Roy\, Deciphering gene regulatory networks underlying cell-fate specification
DESCRIPTION:Abstract: Cell fate specification is a dynamic process during which gene regulatory networks (GRNs) transition between different states and define cell type-specific patterns of gene expression. Identifying such cell type-specific gene regulatory networks is important for understanding how cells differentiate to diverse lineages from a progenitor state\, how differentiated cells can be reprogrammed\, and how these networks get disrupted in diseases such as cancer and developmental disorders. The advent of single cell omics has enabled us to perform high-throughput molecular phenotyping of individual cells at different omic levels. These technologies have revolutionized our understanding of cell type composition across diverse normal and disease conditions; however inferring cell type-specific networks and their dynamics from single cell omic datasets is an open challenge. I will present some of our recent efforts for inference and analysis of cell type-specific regulatory networks from single cell omic datasets. Application of our approach to hematopoietic differentiation and mouse cellular reprogramming predicted key regulatory nodes likely important for establishing different cell-type specific expression programs.
URL:https://www.ibs.re.kr/bimag/event/tbd-2/
LOCATION:ZOOM ID: 997 8258 4700 (Biomedical Mathematics Online Colloquium)\, (pw: 1234)
CATEGORIES:Biomedical Mathematics Online Colloquium
ATTACH;FMTTYPE=image/png:https://www.ibs.re.kr/bimag/cms/wp-content/uploads/2023/02/srpic-1.png
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230609T140000
DTEND;TZID=Asia/Seoul:20230609T160000
DTSTAMP:20260425T235747
CREATED:20230529T032327Z
LAST-MODIFIED:20230608T050231Z
UID:7805-1686319200-1686326400@www.ibs.re.kr
SUMMARY:Seokjoo Chae\, The energy cost and optimal design of networks for biological discrimination
DESCRIPTION:We will discuss about “The energy cost and optimal design of networks for biological discrimination”\, Yu\, Qiwei\, Anatoly B. Kolomeisky\, and Oleg A. Igoshin.\, Journal of the Royal Society Interface 19.188 (2022): 20210883. \nAbstract \n\n\nMany biological processes discriminate between correct and incorrect substrates through the kinetic proofreading mechanism that enables lower error at the cost of higher energy dissipation. Elucidating physico-chemical constraints for global minimization of dissipation and error is important for understanding enzyme evolution. Here\, we identify theoretically a fundamental error–cost bound that tightly constrains the performance of proofreading networks under any parameter variations preserving the rate discrimination between substrates. The bound is kinetically controlled\, i.e. completely determined by the difference between the transition state energies on the underlying free energy landscape. The importance of the bound is analysed for three biological processes. DNA replication by T7 DNA polymerase is shown to be nearly optimized\, i.e. its kinetic parameters place it in the immediate proximity of the error–cost bound. The isoleucyl-tRNA synthetase (IleRS) of E. coli also operates close to the bound\, but further optimization is prevented by the need for reaction speed. In contrast\, E. coli ribosome operates in a high-dissipation regime\, potentially in order to speed up protein production. Together\, these findings establish a fundamental error–dissipation relation in biological proofreading networks and provide a theoretical framework for studying error–dissipation trade-off in other systems with biological discrimination.
URL:https://www.ibs.re.kr/bimag/event/2023-06-09-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:20230612T120000
DTEND;TZID=Asia/Seoul:20230612T130000
DTSTAMP:20260425T235747
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
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20230619T120000
DTEND;TZID=Asia/Seoul:20230619T130000
DTSTAMP:20260425T235747
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:20230622T140000
DTEND;TZID=Asia/Seoul:20230622T160000
DTSTAMP:20260425T235747
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
END:VCALENDAR