BEGIN:VCALENDAR
VERSION:2.0
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:20200101T000000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20210401T120000
DTEND;TZID=Asia/Seoul:20210401T130000
DTSTAMP:20260510T122415
CREATED:20210331T003338Z
LAST-MODIFIED:20210406T075108Z
UID:4352-1617278400-1617282000@www.ibs.re.kr
SUMMARY:Yun Min Song\, A stochastic oscillator model simulates the entrainment of vertebrate cellular clocks by light
DESCRIPTION:We will discuss about “A stochastic oscillator model simulates the entrainment of vertebrate cellular clocks by light”\, Kumpost et al.\, bioRxiv (2021) \nThe circadian clock is a cellular mechanism that synchronizes various biological processes with respect to the time of the day. While much progress has been made characterizing the molecular mechanisms underlying this clock\, it is less clear how external light cues influence the dynamics of the core clock mechanism and thereby entrain it with the light-dark cycle. Zebrafish-derived cell cultures possess clocks that are directly light-entrainable\, thus providing an attractive laboratory model for circadian entrainment. Here\, we have developed a stochastic oscillator model of the zebrafish circadian clock\, which accounts for the core clock negative feedback loop\, light input\, and the proliferation of single-cell oscillator noise into population-level luminescence recordings. The model accurately predicts the entrainment dynamics observed in bioluminescent clock reporter assays upon exposure to a wide range of lighting conditions. Furthermore\, we have applied the model to obtain refitted parameter sets for cell cultures exposed to a variety of pharmacological treatments and predict changes in single-cell oscillator parameters. Our work paves the way for model-based\, large-scale screens for genetic or pharmacologically-induced modifications to the entrainment of circadian clock function.
URL:https://www.ibs.re.kr/bimag/event/2021-04-02/
LOCATION:B305 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:20210409T120000
DTEND;TZID=Asia/Seoul:20210409T130000
DTSTAMP:20260510T122415
CREATED:20210323T105030Z
LAST-MODIFIED:20210407T041048Z
UID:4304-1617969600-1617973200@www.ibs.re.kr
SUMMARY:Highly accurate fluorogenic DNA sequencing with information theory–based error correction
DESCRIPTION:We will discuss about “Highly accurate fluorogenic DNA sequencing with information theory–based error correction”\, Chen et al.\, Nature Biotechnology (2017) \nEliminating errors in next-generation DNA sequencing has proved challenging. Here we present error-correction code (ECC) sequencing\, a method to greatly improve sequencing accuracy by combining fluorogenic sequencing-by-synthesis (SBS) with an information theory–based error-correction algorithm. ECC embeds redundancy in sequencing reads by creating three orthogonal degenerate sequences\, generated by alternate dual-base reactions. This is similar to encoding and decoding strategies that have proved effective in detecting and correcting errors in information communication and storage. We show that\, when combined with a fluorogenic SBS chemistry with raw accuracy of 98.1%\, ECC sequencing provides single-end\, error-free sequences up to 200 bp. ECC approaches should enable accurate identification of extremely rare genomic variations in various applications in biology and medicine. \n  \n 
URL:https://www.ibs.re.kr/bimag/event/2021-04-09/
LOCATION:B305 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:20210415T110000
DTEND;TZID=Asia/Seoul:20210415T120000
DTSTAMP:20260510T122415
CREATED:20210314T044747Z
LAST-MODIFIED:20210412T021311Z
UID:4258-1618484400-1618488000@www.ibs.re.kr
SUMMARY:Dynamics-based data science in biology
DESCRIPTION:This talk will be presented online. Zoom link: 709 120 4849 (pw: 1234) \nAbstract: Life science has been a prosperous subject for a long time\, and is still developing with high speed now. One of its major aims is to study the mechanisms of various biological processes on the basis of biological big-data. Many statistics-based methods have been proposed to catch the essence by mining those data\, including the popular category classification\, variables regression\, group clustering\, statistical comparison\, dimensionality reduction\, and component analysis\, which\, however\, mainly elucidate static features or steady behavior of living organisms due to lack of temporal data. But\, a biological system is inherently dynamic\, and with increasingly accumulated time-series data\, dynamics-based approaches based on physical and biological laws are demanded to reveal dynamic features or complex behavior of biological systems. In this talk\, I will present a new concept “dynamics-based data science” and the approaches for studying dynamical bio-processes\, including dynamical network biomarkers (DNB)\, autoreservoir neural networks (ARNN) and partical cross-mapping. These methods are all data-driven or model-free approaches but based on the theoretical frameworks of nonlinear dynamics. We show the principles and advantages of dynamics-based data-driven approaches as explicable\, quantifiable\, and generalizable. In particular\, dynamics-based data science approaches exploit the essential features of dynamical systems in terms of data\, e.g. strong fluctuations near a bifurcation point\, low-dimensionality of a center manifold or an attractor\, and phase-space reconstruction from a single variable by delay embedding theorem\, and thus are able to provide different or additional information to the traditional approaches\, i.e. statistics-based data science approaches. The dynamical-based data science approaches will further play an important role in the systematical research of biology and medicine in future.
URL:https://www.ibs.re.kr/bimag/event/2021-04-15/
LOCATION:ZOOM ID: 709 120 4849 (ibsbimag)\, (pw: 1234)
CATEGORIES:Biomedical Mathematics Online Colloquium
ATTACH;FMTTYPE=image/jpeg:https://www.ibs.re.kr/bimag/cms/wp-content/uploads/2021/03/LC_profile2.jpg
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20210415T163000
DTEND;TZID=Asia/Seoul:20210415T170000
DTSTAMP:20260510T122415
CREATED:20210411T124649Z
LAST-MODIFIED:20210412T013301Z
UID:4426-1618504200-1618506000@www.ibs.re.kr
SUMMARY:Mathematical modeling for infectious disease using epidemiological data
DESCRIPTION:Abstract: TBA
URL:https://www.ibs.re.kr/bimag/event/2021-04-15_1/
LOCATION:B305 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Biomedical Mathematics Seminar
ATTACH;FMTTYPE=image/jpeg:https://www.ibs.re.kr/bimag/cms/wp-content/uploads/2021/04/HJL_profile5.jpg
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20210415T170000
DTEND;TZID=Asia/Seoul:20210415T173000
DTSTAMP:20260510T122415
CREATED:20210411T124935Z
LAST-MODIFIED:20210412T012752Z
UID:4429-1618506000-1618507800@www.ibs.re.kr
SUMMARY:Practical considerations for measuring the effective reproductive number
DESCRIPTION:Abstract: TBA
URL:https://www.ibs.re.kr/bimag/event/2021-04-15_2/
LOCATION:B305 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Biomedical Mathematics Seminar
ATTACH;FMTTYPE=image/jpeg:https://www.ibs.re.kr/bimag/cms/wp-content/uploads/2021/04/SHC_profile2.jpg
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20210416T120000
DTEND;TZID=Asia/Seoul:20210416T130000
DTSTAMP:20260510T122415
CREATED:20210412T110458Z
LAST-MODIFIED:20210412T110458Z
UID:4423-1618574400-1618578000@www.ibs.re.kr
SUMMARY:Synthetic multistability in mammalian cells
DESCRIPTION:We will discuss about “Synthetic multistability in mammalian cells”\, Zhu et al.\, bioRxiv (2021) \nIn multicellular organisms\, gene regulatory circuits generate thousands of molecularly distinct\, mitotically heritable states\, through the property of multistability. Designing synthetic multistable circuits would provide insight into natural cell fate control circuit architectures and allow engineering of multicellular programs that require interactions among cells in distinct states. Here we introduce MultiFate\, a naturally-inspired\, synthetic circuit that supports long-term\, controllable\, and expandable multistability in mammalian cells. MultiFate uses engineered zinc finger transcription factors that transcriptionally self-activate as homodimers and mutually inhibit one another through heterodimerization. Using model-based design\, we engineered MultiFate circuits that generate up to seven states\, each stable for at least 18 days. MultiFate permits controlled state-switching and modulation of state stability through external inputs\, and can be easily expanded with additional transcription factors. Together\, these results provide a foundation for engineering multicellular behaviors in mammalian cells. \n  \n 
URL:https://www.ibs.re.kr/bimag/event/2021-04-16/
LOCATION:B305 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:20210421T170000
DTEND;TZID=Asia/Seoul:20210421T183000
DTSTAMP:20260510T122415
CREATED:20210324T050549Z
LAST-MODIFIED:20210421T074343Z
UID:4307-1619024400-1619029800@www.ibs.re.kr
SUMMARY:Advice to my younger self
DESCRIPTION:This talk will be presented online. Zoom link: 709 120 4849 (pw: 1234) \nFacebook live streaming: https://www.facebook.com/10226475900150025/videos/10226475902790091 \nAge brings the benefit of experience and looking back at my job as a professor\, there are a couple of things that fall into the category “I wish someone had told me that earlier”. In this seminar\, I would like to share some of the things I learned and which\, I hope\, will be useful for younger scientists. \nThe questions I will touch upon include \n\n\n\nWhat is productivity\, for a scientist?\nWhat are qualities of successful people?\nHow can one create motivation and success?\nHow to organize myself? (project management; getting things done)\nHow to communicate effectively?\nSeeking fulfillment\n\n\n\nThe seminar is targeted at PhD students\, postdocs\, and junior group leaders. \n \n 
URL:https://www.ibs.re.kr/bimag/event/2021-04-21/
LOCATION:ZOOM ID: 709 120 4849 (ibsbimag)\, (pw: 1234)
CATEGORIES:Biomedical Mathematics Online Colloquium
ATTACH;FMTTYPE=image/jpeg:https://www.ibs.re.kr/bimag/cms/wp-content/uploads/2021/03/olaf-wolkenhauer-e1617756681631.jpg
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20210422T120000
DTEND;TZID=Asia/Seoul:20210422T130000
DTSTAMP:20260510T122415
CREATED:20210417T101617Z
LAST-MODIFIED:20210419T021327Z
UID:4477-1619092800-1619096400@www.ibs.re.kr
SUMMARY:A Simple and Flexible Computational Framework for Inferring Sources of Heterogeneity from Single-Cell Dynamics
DESCRIPTION:We will discuss about “A Simple and Flexible Computational Framework for\nInferring Sources of Heterogeneity from Single-Cell\nDynamics”\, Dharmarajan et al.\, Cell Systems (2019) \nSingle-cell time-lapse data provide the means for disentangling sources of cell-to-cell and intra-cellular variability\, a key step for understanding heterogeneity in cell populations. However\, single-cell analysis with dynamic models is a challenging open problem: current inference methods address only single-gene expression or neglect parameter correlations. We report on a simple\, flexible\, and scalable method for estimating cell-specific and population-average parameters of non-linear mixed-effects models of cellular networks\, demonstrating its accuracy with a published model and dataset. We also propose sensitivity analysis for identifying which biological sub-processes quantitatively and dynamically contribute to cell-to-cell variability. Our application to endocytosis in yeast demonstrates that dynamic models of realistic size can be developed for the analysis of single-cell data and that shifting the focus from single reactions or parameters to nuanced and time-dependent contributions of sub-processes helps biological interpretation. Generality and simplicity of the approach will facilitate customized extensions for analyzing single-cell dynamics
URL:https://www.ibs.re.kr/bimag/event/2021-04-22/
LOCATION:B305 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:20210429T120000
DTEND;TZID=Asia/Seoul:20210429T130000
DTSTAMP:20260510T122415
CREATED:20210425T180554Z
LAST-MODIFIED:20210425T180554Z
UID:4499-1619697600-1619701200@www.ibs.re.kr
SUMMARY:Introduction to Bayesian ML/DL\, with Application to Parameter Inference of Coupled Non-linear ODEs - Part 1
DESCRIPTION:In this talk\, the speaker will present introductory materials about Bayesian Machine Learning. \nAbstract\nGaussian process(GP) is a stochastic process such that the joint distribution of an arbitrary finite subset of the random variables is a multivariate normal. It plays a fundamental role in Bayesian machine learning as it can be interpreted as a prior over functions (Rasmussen and Williams\, 2006)\, hence providing a nonparametric approach to various tasks. In the first part\, I will introduce the general framework of GP and some underlying theory\, accompanied by an illustrative example of GP regression\, also known as Kringing. In the second part\, I will introduce some recent works on applying GP to parameter inference of coupled non-linear ODEs arising in various biological contexts.
URL:https://www.ibs.re.kr/bimag/event/introduction-to-bayesian-ml-dl-with-application-to-parameter-inference-of-coupled-non-linear-odes-part-1/
LOCATION:B305 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:20210430T160000
DTEND;TZID=Asia/Seoul:20210430T170000
DTSTAMP:20260510T122415
CREATED:20210319T021820Z
LAST-MODIFIED:20210412T013739Z
UID:4282-1619798400-1619802000@www.ibs.re.kr
SUMMARY:What is the role of oscillatory signals in intracellular systems?
DESCRIPTION:Oscillatory signals are ubiquitously observed in many different intracellular systems such as immune systems and DNA repair processes. While we know how oscillatory signals are created\, we do not fully understand what a critical role they play to regulate signal pathway systems in cells. Recently by using a stochastic nucleosome system\, we found that a special signal (NFkB signal) in an immune cell can enhance the variability of the immune response to inflammatory stimulations when the signal is oscillatory. Hence in this talk\, we discuss the roles of oscillatory and non-oscillatory NFkB signals in an inflammatory system of immune cells as the main example for revealing the role of oscillatory signals. And then we will talk about how this finding can be generalized for other intra- or extra-cellular systems to study why cells use oscillations.
URL:https://www.ibs.re.kr/bimag/event/2021-04-30/
LOCATION:B305 Seminar room\, IBS\, 55 Expo-ro Yuseong-gu\, Daejeon\, 34126\, Korea\, Republic of
CATEGORIES:Biomedical Mathematics Seminar
ATTACH;FMTTYPE=image/jpeg:https://www.ibs.re.kr/bimag/cms/wp-content/uploads/2021/03/Jinsu-Kim-9-e1617756454410.jpeg
ORGANIZER;CN="Jae Kyoung Kim":MAILTO:jaekkim@kaist.ac.kr
END:VEVENT
END:VCALENDAR