{"lab": {"title": "Job Dekker, UMMS", "@id": "/labs/job-dekker-lab/", "status": "current", "display_title": "Job Dekker, UMMS", "@type": ["Lab", "Item"], "correspondence": [{"contact_email": "am9iLmRla2tlckB1bWFzc21lZC5lZHU=", "@id": "/users/83b5073a-069b-4162-9b30-6f42d5551e34/", "display_title": "Job Dekker"}], "uuid": "3c577664-affb-41c4-bf27-9e21c2fc1554", "pi": {"error": "no view permissions"}, "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin", "role.lab_submitter", "submits_for.3c577664-affb-41c4-bf27-9e21c2fc1554"]}}, "award": {"uuid": "ae6c618f-7a8c-441e-a886-e30bbbe591da", "@id": "/awards/1U54DK107980-01/", "@type": ["Award", "Item"], "project": "4DN", "center_title": "NOFIC - Dekker", "description": "NOFIC: The spatial organization of the genome impinges on all genomic processes, including gene regulation, maintenance of genome stability and chromosome transmission to daughter cells. A detailed understanding of the spatial arrangement of the human genome, referred to as the 4D nucleome, and the biological and physical principles that drive chromosome folding requires combining approaches from the fields of molecular and cell biology, imaging, genetics and genomics with approaches from physics, computational biology, and computer simulation. We have assembled a highly interdisciplinary center with the goal of generating extensively validated maps of the 4D nucleome, its physical and dynamic properties and its role in regulating the activity of the genome. First, the center will further optimize and extensively validate a suite of genome-wide molecular methodologies, based on chromosome conformation capture (3C) that can probe the folding of chromosomes at the scale of single nucleosomes, chromatin fibers, chromosomes and the entire nucleus, across cell populations and in single cells. Given that chromosome and nuclear organization is tightly linked to biological state of the cell, the center will map the 4D nucleome for four key biological states representing different conformations during the cell cycle (interphase and mitosis), and during cell differentiation (pluripotent and differentiated states). We will obtain complementary data regarding the structure and dynamics of chromatin, at different length scales and in single cells using extensive high-throughput imaging, live cell imaging and super resolution microscopy. Data obtained with all approaches will be analyzed, integrated and modeled using a set of methods we will further develop to gain insights into the structure, physics and dynamics of chromosome folding over different length scales. Finally, a critical component of our proposal is the biological validation and further elaboration of the chromatin interaction maps that are generated from our conformational analyses. This validation will be achieved through site-specific editing of genomic sequence and epigenetic marks, the creation of new contact points within the genome, and the identification of factors (both protein and nucleic acid) that facilitat or restrict these interactions. 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Nuclei were purified before performing Hi-C 2.0.", "study_group": "Disrupted or Atypical Cells", "date_created": "2019-06-04T14:11:56.942967+00:00", "submitted_by": {"error": "no view permissions"}, "dataset_label": "Liquified Chromatin Hi-C on K562 cells", "last_modified": {"modified_by": {"error": "no view permissions"}, "date_modified": "2021-02-23T14:46:01.112028+00:00"}, "public_release": "2019-11-04", "replicate_exps": [{"bio_rep_no": 1, "tec_rep_no": 1, "replicate_exp": {"display_title": "in situ Hi-C on K562 (Tier 2) with HindIII - 4DNEXN2AO8PE", "@id": "/experiments-hi-c/4DNEXN2AO8PE/", "@type": ["ExperimentHiC", "Experiment", "Item"], "accession": "4DNEXN2AO8PE", "uuid": "9494dc72-6bfe-4a37-b5b2-47352055b5dc", "status": "released", "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin"]}}}], "schema_version": "2", "static_content": [{"content": {"contributing_labs": [], "display_title": "4DNESR93N4E3 - Processed files", "name": "ad34f9ff-36fc-4ca1-a858-4f8901166f03", "description": "4DNESR93N4E3 (These are biological replicate in which we performed Liquid chromatin Hi-C on K652 cells. 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Compared to standard dilution Hi-C, this technique reduces the frequency of random ligation because the ligation is performed <i>in situ</i> inside the nucleus, a constrained space, instead of in solution, where DNA fragments are floating freely. In addition, this protocol can be done more quickly in the lab and was the first to introduce the use of 4-cutter restriction enzymes as opposed to the previous 6-cutters, providing higher resolution.\n</p>\n<p>\nThe protocol involves cross-linking the cells with formaldehyde to form links between physically adjacent DNA regions. The cells are then permeabilized with their nuclei intact. A 4-cutter restriction enzyme is used to digest the chromatin into multiple DNA fragments. The resulting fragments are biotinylated by end filling of the fragments ends. The fragments are then ligated and the DNA is purified and sheared. 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This duplication does not affect the higlass display of these files, howevver, downstream analyses using this file may encounter issues due to this pixel duplication.  The counts from the duplicate pixels can be aggregated to determine the correct count value at that location. If this issue is problematic for your needs you should consider regenerating the matrices from the merged pairs file of the associated dataset using a more recent version of cooler.  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Liquid chromatin Hi-C provides a genome-wide view of chromosome interaction dynamics.", "uuid": "f9f934ef-245e-4f66-9a1c-7287f36b0c80", "date_published": "2021-02-11", "url": "https://www.ncbi.nlm.nih.gov/pubmed/33574602", "journal": "Nature genetics", "title": "Liquid chromatin Hi-C characterizes compartment-dependent chromatin interaction dynamics.", "status": "current", "short_attribution": "Belaghzal H et al. (2021)", "ID": "PMID:33574602", "display_title": "Belaghzal H et al. (2021) PMID:33574602", "@id": "/publications/f9f934ef-245e-4f66-9a1c-7287f36b0c80/", "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin"]}}, "pubs_using": [], "publications_of_set": [{"title": "Liquid chromatin Hi-C characterizes compartment-dependent chromatin interaction dynamics.", "journal": "Nature genetics", "@type": ["Publication", "Item"], "display_title": "Belaghzal H et al. (2021) PMID:33574602", "authors": ["Belaghzal H", "Borrman T", "Stephens AD", "Lafontaine DL", "Venev SV", "Weng Z", "Marko JF", "Dekker J"], "abstract": "Nuclear compartmentalization of active and inactive chromatin is thought to occur through microphase separation mediated by interactions between loci of similar type. The nature and dynamics of these interactions are not known. We developed liquid chromatin Hi-C to map the stability of associations between loci. Before fixation and Hi-C, chromosomes are fragmented, which removes strong polymeric constraint, enabling detection of intrinsic locus-locus interaction stabilities.  Compartmentalization is stable when fragments are larger than 10-25 kb. Fragmentation of chromatin into pieces smaller than 6 kb leads to gradual loss of genome organization. Lamin-associated domains are most stable, whereas interactions for speckle- and polycomb-associated loci are more dynamic. Cohesin-mediated loops dissolve after fragmentation. Liquid chromatin Hi-C provides a genome-wide view of chromosome interaction dynamics.", "date_published": "2021-02-11", "uuid": "f9f934ef-245e-4f66-9a1c-7287f36b0c80", "status": "current", "@id": "/publications/f9f934ef-245e-4f66-9a1c-7287f36b0c80/", "ID": "PMID:33574602", "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin"]}}], "number_of_experiments": 1, "@context": "/terms/", "aggregated-items": {"badges": [{"parent": "/biosamples/4DNBSA1HHFHR/", "embedded_path": "experiments_in_set.biosample.badges", "item": {"messages": ["Biosample missing morphology_image"], "badge": {"commendation": null, "warning": "Biosample Metadata Incomplete", "uuid": "2b2cc7ff-b7a8-4138-9a6c-22884fc71690", "@id": "/badges/biosample-metadata-incomplete/", "badge_icon": "/static/img/badges/biosample-icon.svg", "description": "Biosample is missing metadata information required as part of the standards implemented by the 4DN Samples working group."}}}, {"parent": "/experiment-set-replicates/4DNESR93N4E3/", "embedded_path": "badges", "item": {"messages": ["Replicate set contains only a single biological replicate"], "badge": {"commendation": null, "warning": "Replicate Numbers", "uuid": "24a64a84-3c33-4d76-aaf2-e5ef45eff347", "@id": "/badges/replicate-numbers/", "badge_icon": "/static/img/badges/replicates-orange-circle.svg", "description": "Issues with replicate numbers"}}}]}, "validation-errors": []}