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:20220101T000000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20231201T140000
DTEND;TZID=Asia/Seoul:20231201T160000
DTSTAMP:20260425T052208
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:20231208T153000
DTEND;TZID=Asia/Seoul:20231208T173000
DTSTAMP:20260425T052208
CREATED:20231130T084548Z
LAST-MODIFIED:20231207T014408Z
UID:8751-1702049400-1702056600@www.ibs.re.kr
SUMMARY:Olive Cawiding\, Time delays modulate the stability of complex ecosystems
DESCRIPTION:We will discuss about “Time delays modulate the stability of complex ecosystems” Nature Ecology & Evolution 7.10 (2023): 1610-1619. \nAbstract \nWhat drives the stability\, or instability\, of complex ecosystems? This question sits at the heart of community ecology and has motivated a large body of theoretical work exploring how community properties shape ecosystem dynamics. However\, the overwhelming majority of current theory assumes that species interactions are instantaneous\, meaning that changes in the abundance of one species will lead to immediate changes in the abundances of its partners. In practice\, time delays in how species respond to one another are widespread across ecological contexts\, yet the impact of these delays on ecosystems remains unclear. Here we derive a new body of theory to comprehensively study the impact of time delays on ecological stability. We find that time delays are important for ecosystem stability. Large delays are typically destabilizing but\, surprisingly\, short delays can substantially increase community stability. Moreover\, in stark contrast to delay-free systems\, delays dictate that communities with more abundant species can be less stable than ones with less abundant species. Finally\, we show that delays fundamentally shift how species interactions impact ecosystem stability\, with communities of mixed interaction types becoming the most stable class of ecosystem. Our work demonstrates that time delays can be critical for the stability of complex ecosystems. \n 
URL:https://www.ibs.re.kr/bimag/event/2023-12-08-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:20231215T140000
DTEND;TZID=Asia/Seoul:20231215T160000
DTSTAMP:20260425T052208
CREATED:20231130T085305Z
LAST-MODIFIED:20231214T000605Z
UID:8758-1702648800-1702656000@www.ibs.re.kr
SUMMARY:Yun Min Song\, Pulsed stimuli entrain p53 to synchronize single cells and modulate cell-fate determination
DESCRIPTION:We will discuss about “Pulsed stimuli entrain p53 to synchronize single cells and modulate cell-fate determination” bioRxiv (2023): 2023-10. \nAbstract \n\n\nEntrainment to an external stimulus enables a synchronized oscillatory response across a population of cells\, increasing coherent responses by reducing cell-to-cell heterogeneity. It is unclear whether the property of entrainability extends to systems where responses are intrinsic to the individual cell\, rather than dependent on coherence across a population of cells. Using a combination of mathematical modeling\, time-lapse fluorescence microscopy\, and single-cell tracking\, we demonstrated that p53 oscillations triggered by DNA double-strand breaks (DSBs) can be entrained with a periodic damage stimulus\, despite such synchrony not known to function in effective DNA damage responses. Surprisingly\, p53 oscillations were experimentally entrained over a wider range of DSB frequencies than predicted by an established computational model for the system. We determined that recapitulating the increased range of entrainment frequencies required\, non-intuitively\, a less robust oscillator and wider steady-state valley on the energy landscape. Further\, we show that p53 entrainment can lead to altered expression dynamics of downstream targets responsible for cell fate in a manner dependent on target mRNA stability. Overall\, this study demonstrates that entrainment can occur in a biological oscillator despite the apparent lack of an evolutionary advantage conferred through synchronized responses and highlights the potential of externally entraining p53 dynamics to reduce cellular variability and synchronize cell-fate responses for therapeutic outcomes.
URL:https://www.ibs.re.kr/bimag/event/2023-12-15-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:20231229T140000
DTEND;TZID=Asia/Seoul:20231229T160000
DTSTAMP:20260425T052208
CREATED:20231130T085100Z
LAST-MODIFIED:20231228T025820Z
UID:8756-1703858400-1703865600@www.ibs.re.kr
SUMMARY:Hyun Kim\, MultiVI: deep generative model for the integration of multimodal data
DESCRIPTION:We will discuss about “MultiVI: deep generative model for the integration of multimodal data” Nature Methods 20.8 (2023): 1222-1231. \nAbstract \n\n\n\nJointly profiling the transcriptome\, chromatin accessibility and other molecular properties of single cells offers a powerful way to study cellular diversity. Here we present MultiVI\, a probabilistic model to analyze such multiomic data and leverage it to enhance single-modality datasets. MultiVI creates a joint representation that allows an analysis of all modalities included in the multiomic input data\, even for cells for which one or more modalities are missing. It is available at scvi-tools.org.
URL:https://www.ibs.re.kr/bimag/event/2023-12-29-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