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PHASE II", "@type": ["Award", "Item"], "uuid": "71171a4e-dca1-44cb-8375-fafd896c6923", "status": "current", "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin"]}}, "filetype": "md", "name": "delaat-ext-grant-note", "lab": {"status": "current", "uuid": "828cd4fe-ebb0-4b36-a94a-d2e3a36cc989", "@id": "/labs/4dn-dcic-lab/", "@type": ["Lab", "Item"], "display_title": "4DN DCIC, HMS", "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin", "role.lab_submitter", "submits_for.828cd4fe-ebb0-4b36-a94a-d2e3a36cc989"]}}, "content_as_html": "<div class=\"markdown-container\"><p>This work was supported by Fondation Leducq (14CVD01) Transatlantic Network grant: \u2018Deciphering the genomic topology of atrial fibrillation\u2019</p></div>", "status": "released", "@id": "/static-sections/5ea459cc-cbfa-4d8e-897c-29bebbfd3c33/", "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin", "role.owner", "userid.986b362f-4eb6-4a9c-8173-3ab267227777"]}}, "location": "tab:attribution"}], "static_headers": [{"lab": {"display_title": "4DN DCIC, HMS", "@id": "/labs/4dn-dcic-lab/", "@type": ["Lab", "Item"], "uuid": "828cd4fe-ebb0-4b36-a94a-d2e3a36cc989", "status": "current", "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin", "role.lab_submitter", "submits_for.828cd4fe-ebb0-4b36-a94a-d2e3a36cc989"]}}, "body": "<b>In Situ Hi-C</b>\n\n<p>\n   In situ Hi-C is a method to detect and quantify the pairwise interactions between chromosome regions across the entire genome. 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(2019) doi:10.1101/705715", "uuid": "395b511a-5db1-4080-b5a7-b180769b7328", "authors": ["Bianchi V", "Geeven G", "Tucker N", "Hilvering CRE", "Hall AW", "Roselli C", "Hill MC", "Martin JF", "Margulies KB", "Ellinor PT", "deLaat W"], "date_published": "2019-07-17", "short_attribution": "Bianchi V et al. (2019)", "abstract": "Most disease-associated variants identified by population based genetic studies are non-coding, which compromises finding causative genes and mechanisms. Presumably they interact through looping with nearby genes to modulate transcription. Hi-C provides the most complete and unbiased method for genome-wide identification of potential regulatory interactions, but finding chromatin loops in Hi-C data remains difficult and tissue specific data are limited. We have generated Hi-C data from primary cardiac tissue and developed a method, peakHiC, for sensitive and quantitative loop calling to uncover the human heart regulatory interactome. We identify complex CTCF-dependent and -independent contact networks, with loops between coding and non-coding gene promoters, shared enhancers and repressive sites. Across the genome, enhancer interaction strength correlates with gene transcriptional output and loop dynamics follows CTCF, cohesin and H3K27Ac occupancy levels. Finally, we demonstrate that intersection of the human heart regulatory interactome with cardiovascular disease variants facilitates prioritizing disease-causative genes.", "ID": "doi:10.1101/705715", "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin"]}}, "pubs_using": [], "publications_of_set": [{"date_published": "2019-07-17", "ID": "doi:10.1101/705715", "status": "current", "@type": ["Publication", "Item"], "@id": "/publications/395b511a-5db1-4080-b5a7-b180769b7328/", "authors": ["Bianchi V", "Geeven G", "Tucker N", "Hilvering CRE", "Hall AW", "Roselli C", "Hill MC", "Martin JF", "Margulies KB", "Ellinor PT", "deLaat W"], "uuid": "395b511a-5db1-4080-b5a7-b180769b7328", "title": "Detailed Regulatory Interaction Map of the Human Heart Facilitates Gene Discovery for Cardiovascular Disease", "display_title": "Bianchi V et al. 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Across the genome, enhancer interaction strength correlates with gene transcriptional output and loop dynamics follows CTCF, cohesin and H3K27Ac occupancy levels. Finally, we demonstrate that intersection of the human heart regulatory interactome with cardiovascular disease variants facilitates prioritizing disease-causative genes.", "journal": "bioRxiv", "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin"]}}], "number_of_experiments": 2, "@context": "/terms/", "aggregated-items": {"badges": []}, "validation-errors": []}