Please use this identifier to cite or link to this item: https://doi.org/10.1093/hmg/ddac079
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dc.titleIntegrative multi-omics database (iMOMdb) of Asian pregnant women
dc.contributor.authorHong Pan
dc.contributor.authorPei Fang Tan
dc.contributor.authorIves Y. Lim
dc.contributor.authorJason Huan
dc.contributor.authorAi Ling Teh
dc.contributor.authorLi Chen
dc.contributor.authorMin Gong
dc.contributor.authorFelicia Tin
dc.contributor.authorSartaj Ahmad Mir
dc.contributor.authorKothandaraman Narasimhan
dc.contributor.authorChan, J.K.Y.
dc.contributor.authorTan, K.H.
dc.contributor.authorMichael S. Kobor
dc.contributor.authorPeter J. Meikle
dc.contributor.authorMarkus R. Wenk
dc.contributor.authorChong, Y.S.
dc.contributor.authorEriksson, J.G.
dc.contributor.authorPeter D. Gluckman
dc.contributor.authorKarnani, N.
dc.date.accessioned2022-07-08T08:12:22Z
dc.date.available2022-07-08T08:12:22Z
dc.date.issued2022
dc.identifier.citationHong Pan, Pei Fang Tan, Ives Y. Lim, Jason Huan, Ai Ling Teh, Li Chen, Min Gong, Felicia Tin, Sartaj Ahmad Mir, Kothandaraman Narasimhan, Chan, J.K.Y., Tan, K.H., Michael S. Kobor, Peter J. Meikle, Markus R. Wenk, Chong, Y.S., Eriksson, J.G., Peter D. Gluckman, Karnani, N. (2022). Integrative multi-omics database (iMOMdb) of Asian pregnant women. Human Molecular Genetics. ScholarBank@NUS Repository. https://doi.org/10.1093/hmg/ddac079
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/228137
dc.description.abstractAsians are underrepresented across many omics databases, thereby limiting the potential of precision medicine in nearly 60% of the global population. As such, there is a pressing need for multi-omics derived quantitative trait loci (QTLs) to fill the knowledge gap of complex traits in populations of Asian ancestry. Here, we provide the first blood-based multi-omics analysis of Asian pregnant women, constituting high-resolution genotyping (N = 1079), DNA methylation (N = 915) and transcriptome profiling (N = 238). Integrative omics analysis identified 219 154 CpGs associated with cis-DNA methylation QTLs (meQTLs) and 3703 RNAs associated with cis-RNA expression QTLs (eQTLs). Ethnicity was the largest contributor of inter-individual variation across all omics datasets, with 2561 genes identified as hotspots of this variation; 395 of these hotspot genes also contained both ethnicity-specific eQTLs and meQTLs. Gene set enrichment analysis of these ethnicity QTL hotspots showed pathways involved in lipid metabolism, adaptive immune system and carbohydrate metabolism. Pathway validation by profiling the lipidome (?480 lipids) of antenatal plasma (N = 752) and placenta (N = 1042) in the same cohort showed significant lipid differences among Chinese, Malay and Indian women, validating ethnicity-QTL gene effects across different tissue types. To develop deeper insights into the complex traits and benefit future precision medicine research in Asian pregnant women, we developed iMOMdb, an open-access database.
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.contributor.departmentDEAN'S OFFICE (DUKE-NUS MEDICAL SCHOOL)
dc.contributor.departmentDEAN'S OFFICE (MEDICINE)
dc.contributor.departmentOBSTETRICS & GYNAECOLOGY
dc.contributor.departmentBIOCHEMISTRY
dc.description.doi10.1093/hmg/ddac079
dc.description.sourcetitleHuman Molecular Genetics
dc.published.statePublished
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