Evidence map›Paper›PMID 30586358›Full record

ArticlePLoS genetics2018

Walking along chromosomes with super-resolution imaging, contact maps, and integrative modeling.

Guy Nir, Irene Farabella, Cynthia Pérez Estrada, Carl G Ebeling, Brian J Beliveau, Hiroshi M Sasaki, S Dean Lee, Son C Nguyen, Ruth B McCole, Shyamtanu Chattoraj and 19 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 160 papers.

0numbers the graph read from it
0cells of the map it votes in
160citing papers in PubMed
49.8field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

160 citing papers in PubMed, 285 citations in OpenAlex.

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  9. An electrostatic repulsion model of centromere organisation.bioRxiv : the preprint server for biology · 2025
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100 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

29 authors at 8 institutions in 2 countries.

Guy NirDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0001-9268-6596
Irene FarabellaCNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
Cynthia Pérez EstradaDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.
Carl G EbelingBruker Nano Inc., Salt Lake City, Utah, United States of America.ORCID 0000-0003-0536-026X
Brian J BeliveauDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0003-1314-3118
Hiroshi M SasakiWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, Massachusetts, United States of America.ORCID 0000-0001-9201-8766
S Dean LeeDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0001-6391-9821
Son C NguyenDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0003-2187-1027
Ruth B McColeDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0002-1861-7055
Shyamtanu ChattorajDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0001-8596-296X
Jelena ErcegDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.
Jumana AlHaj AbedDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0001-5388-1751
Nuno M C MartinsDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0003-3953-9313
Huy Q NguyenDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0003-4675-0520
Mohammed A HannanDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0001-9603-6283
Sheikh RussellCenter for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.ORCID 0000-0003-2998-7817
Neva C DurandCenter for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
Suhas S P RaoCenter for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
Jocelyn Y KishiWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, Massachusetts, United States of America.ORCID 0000-0003-4352-1159
Paula Soler-VilaCNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.ORCID 0000-0003-1741-6670
Michele Di PierroCenter for Theoretical Biological Physics, Rice University, Houston, Texas, United States of America.
José N OnuchicCenter for Theoretical Biological Physics, Rice University, Houston, Texas, United States of America.ORCID 0000-0002-9448-0388
Steven P CallahanZero Epsilon, LLC, Salt Lake City, Utah, United States of America.
John M SchreinerZero Epsilon, LLC, Salt Lake City, Utah, United States of America.ORCID 0000-0003-2829-4402
Jeff A StuckeyBruker Nano Inc., Middleton, Wisconsin, United States of America.ORCID 0000-0002-2130-9387
Peng YinWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, Massachusetts, United States of America.ORCID 0000-0002-4773-359X
Erez Lieberman AidenCenter for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
Marc A Marti-RenomCNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.ORCID 0000-0002-0151-4279
C-Ting WuDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0001-5525-871X
Harvard University · USBaylor College of Medicine · USBroad Institute · USBruker (United States) · USCenter for Theoretical Biological Physics · USCentre for Genomic Regulation · ESEpsilon Systems (United States) · USInstitució Catalana de Recerca i Estudis Avançats · ES

Funding

Culling the human genome of disease variants using ultraconserved elementsR01HD091797 · NICHD · HARVARD MEDICAL SCHOOL · PI WU, CHAO-TING · 2016 to 2020
$5.5M
GENOME WIDE MAPPING OF LOOPS USING IN SITU HI-CUM1HG009375 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI LIEBERMAN-AIDEN, EREZ · 2017 to 2021
$4.7M
The inheritance of position: It's not just who you are, it's where you areDP1GM106412 · NIGMS · HARVARD MEDICAL SCHOOL · PI WU, CHAO-TING · 2012 to 2016
$4.2M
Super-resolution imaging via programmable autonomous blinkingR01EB018659 · NIBIB · HARVARD MEDICAL SCHOOL · PI YIN, PENG · 2013 to 2017
$3.3M
Exploring how the genome folds through proximity ligation and sequencingDP2OD008540 · OD · BROAD INSTITUTE, INC. · PI LIEBERMAN-AIDEN, EREZ · 2011 to 2016
$3.0M
Technologies for visualizing the genome in situR01GM123289 · NIGMS · HARVARD MEDICAL SCHOOL · PI WU, CHAO-TING · 2017 to 2020
$2.5M
Supplement - Beyond pairwise DNA contacts: exploring higher-order genome structure using proximity ligationU01HL130010 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI LIEBERMAN-AIDEN, EREZ · 2015 to 2019
$2.3M
Ultra-Multiplexed Nanoscale In Situ Proteomics for Understanding Synapse TypesU01MH106011 · NIMH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BATHE, MARK, BOYDEN, EDWARD S. · 2014 to 2016
$2.2M
Howard Hughes Medical InstituteNHGRI NIH HHS UM1 HG009375NHLBI NIH HHS U01 HL130010NIBIB NIH HHS R01 EB018659NICHD NIH HHS R01 HD091797NIGMS NIH HHS DP1 GM106412NIGMS NIH HHS R01 GM123289NIH HHS DP2 OD008540NIMH NIH HHS U01 MH106011
6 · The paper itself

Abstract

Chromosome organization is crucial for genome function. Here, we present a method for visualizing chromosomal DNA at super-resolution and then integrating Hi-C data to produce three-dimensional models of chromosome organization. Using the super-resolution microscopy methods of OligoSTORM and OligoDNA-PAINT, we trace 8 megabases of human chromosome 19, visualizing structures ranging in size from a few kilobases to over a megabase. Focusing on chromosomal regions that contribute to compartments, we discover distinct structures that, in spite of considerable variability, can predict whether such regions correspond to active (A-type) or inactive (B-type) compartments. Imaging through the depths of entire nuclei, we capture pairs of homologous regions in diploid cells, obtaining evidence that maternal and paternal homologous regions can be differentially organized. Finally, using restraint-based modeling to integrate imaging and Hi-C data, we implement a method-integrative modeling of genomic regions (IMGR)-to increase the genomic resolution of our traces to 10 kb.

Indexed as

Models, GeneticCells, CulturedChromosome PaintingChromosomes, Human, Pair 19Chromosome StructuresChromosome WalkingFemaleFluorescent DyesHumansImaging, Three-DimensionalIn Situ Hybridization, FluorescenceMaleOligonucleotide ProbesPedigreeFluorescent DyesOligonucleotide Probes

Identifiers

PMID30586358
PMCPMC6324821
OpenAlexW2952052372

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.