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Integration of partially observed multimodal and multiscale neural signals for estimating a neural circuit using dynamic causal modeling
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kang, Jiyoung | - |
| dc.contributor.author | Park, Hae-Jeong | - |
| dc.date.accessioned | 2025-04-17T08:18:11Z | - |
| dc.date.available | 2025-04-17T08:18:11Z | - |
| dc.date.created | 2025-03-31 | - |
| dc.date.issued | 2024-12 | - |
| dc.identifier.issn | 1553-734X | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/204557 | - |
| dc.description.abstract | Integrating multiscale, multimodal neuroimaging data is essential for a comprehensive understanding of neural circuits. However, this is challenging due to the inherent trade-offs between spatial coverage and resolution in each modality, necessitating a computational strategy that combines modality-specific information effectively. This study introduces a dynamic causal modeling (DCM) framework designed to address the challenge of combining partially observed, multiscale signals across a larger-scale neural circuit by employing a shared neural state model with modality-specific observation models. The proposed method achieves robust circuit inference by iteratively integrating parameter estimates from local microscale and global meso- or macroscale circuits, derived from signals across various scales and modalities. Parameters estimated from high-resolution data within specific regions inform global circuit estimation by constraining neural properties in unobserved regions, while large-scale circuit data help elucidate detailed local circuitry. Using a virtual ground truth system, we validated the method across diverse experimental settings, combining calcium imaging (CaI), voltage-sensitive dye imaging (VSDI), and blood-oxygen-level-dependent (BOLD) signals-each with distinct coverage and resolution. Our reciprocal and iterative parameter estimation approach markedly improves the accuracy of neural property and connectivity estimates compared to traditional one-step estimation methods. This iterative integration of local and global parameters presents a reliable approach to inferring extensive, complex neural circuits from partially observed, multimodal, and multiscale data, showcasing how information from different scales reciprocally enhances entire circuit parameter estimation. | - |
| dc.description.statementOfResponsibility | open | - |
| dc.language | English | - |
| dc.publisher | Public Library of Science | - |
| dc.relation.isPartOf | PLOS COMPUTATIONAL BIOLOGY | - |
| dc.relation.isPartOf | PLOS COMPUTATIONAL BIOLOGY | - |
| dc.rights | CC BY-NC-ND 2.0 KR | - |
| dc.title | Integration of partially observed multimodal and multiscale neural signals for estimating a neural circuit using dynamic causal modeling | - |
| dc.type | Article | - |
| dc.contributor.college | College of Medicine (의과대학) | - |
| dc.contributor.department | Dept. of Nuclear Medicine (핵의학교실) | - |
| dc.contributor.googleauthor | Kang, Jiyoung | - |
| dc.contributor.googleauthor | Park, Hae-Jeong | - |
| dc.identifier.doi | 10.1371/journal.pcbi.1012655 | - |
| dc.relation.journalcode | J02537 | - |
| dc.identifier.eissn | 1553-7358 | - |
| dc.identifier.pmid | 39715262 | - |
| dc.contributor.alternativeName | Park, Hae Jeong | - |
| dc.contributor.affiliatedAuthor | Park, Hae-Jeong | - |
| dc.identifier.scopusid | 2-s2.0-85213324341 | - |
| dc.identifier.wosid | 001381882100011 | - |
| dc.citation.volume | 20 | - |
| dc.citation.number | 12 | - |
| dc.identifier.bibliographicCitation | PLOS COMPUTATIONAL BIOLOGY, Vol.20(12), 2024-12 | - |
| dc.identifier.rimsid | 85849 | - |
| dc.type.rims | ART | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.subject.keywordPlus | VSDI | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalWebOfScienceCategory | Biochemical Research Methods | - |
| dc.relation.journalWebOfScienceCategory | Mathematical & Computational Biology | - |
| dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
| dc.relation.journalResearchArea | Mathematical & Computational Biology | - |
| dc.identifier.articleno | e1012655 | - |
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