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:20210101T000000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=Asia/Seoul:20220705T100000
DTEND;TZID=Asia/Seoul:20220705T110000
DTSTAMP:20260425T050442
CREATED:20220704T160000Z
LAST-MODIFIED:20220704T035619Z
UID:6122-1657015200-1657018800@www.ibs.re.kr
SUMMARY:AI Pontryagin or how artificial neural networks learn to control dynamical systems
DESCRIPTION:We will discuss about “AI Pontryagin or how artificial neural networks learn to control dynamical systems”\, Böttcher\, L.\, Antulov-Fantulin\, N. & Asikis\, T.\, Nat Commun 13\, 333 (2022). \nAbstract: The efficient control of complex dynamical systems has many applications in the natural and applied sciences. In most real-world control problems\, both control energy and cost constraints play a significant role. Although such optimal control problems can be formulated within the framework of variational calculus\, their solution for complex systems is often analytically and computationally intractable. To overcome this outstanding challenge\, we present AI Pontryagin\, a versatile control framework based on neural ordinary differential equations that automatically learns control signals that steer high-dimensional dynamical systems towards a desired target state within a specified time interval. We demonstrate the ability of AI Pontryagin to learn control signals that closely resemble those found by corresponding optimal control frameworks in terms of control energy and deviation from the desired target state. Our results suggest that AI Pontryagin is capable of solving a wide range of control and optimization problems\, including those that are analytically intractable
URL:https://www.ibs.re.kr/bimag/event/2022-07-05-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:20220705T160000
DTEND;TZID=Asia/Seoul:20220705T170000
DTSTAMP:20260425T050442
CREATED:20220704T220000Z
LAST-MODIFIED:20220625T051518Z
UID:6240-1657036800-1657040400@www.ibs.re.kr
SUMMARY:TENET+: a tool for reconstructing gene networks by integrating single cell expression and chromatin accessibility data
DESCRIPTION:Reconstruction of gene regulatory networks (GRNs) is a powerful approach to capture a prioritized gene set controlling cellular processes. In our previous study\, we developed TENET a GRN reconstructor from single cell RNA sequencing (scRNAseq). TENET has a superior capability to identify key regulators compared with other algorithms. However\, accurate inference of gene regulation is still challenging. Here\, we suggest an integrative strategy called TENET+ by combining single cell transcriptome and chromatin accessibility data. By applying TENET+ to a paired scRNAseq and scATACseq dataset of human peripheral blood mononuclear cells\, we found critical regulators and their epigenetic regulations for the differentiations of CD4 T cells\, CD8 T cells\, B cells and monocytes. Interestingly\, TENET+ predicted LRRFIP1 and ZBTB16 as top regulators of CD4 and CD8 T cells which were not predicted in a motif-based tool SCENIC. In sum\, TENET+ is a tool predicting epigenetic gene regulatory programs in unbiased way\, suggesting that novel epigenetic regulations can be identified by TENET+.
URL:https://www.ibs.re.kr/bimag/event/2022-07-05-seminar/
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
END:VCALENDAR