Evidence map›Paper›PMID 29382556›Full record

ArticleMethods (San Diego, Calif.)2018

Using DNase Hi-C techniques to map global and local three-dimensional genome architecture at high resolution.

Wenxiu Ma, Ferhat Ay, Choli Lee, Gunhan Gulsoy, Xinxian Deng, Savannah Cook, Jennifer Hesson, Christopher Cavanaugh, Carol B Ware, Anton Krumm and 5 more

Open access · greenAbstract read
In one paragraph

Article in Methods (San Diego, Calif.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. The macro and micro of chromosome conformation capture.Wiley interdisciplinary reviews. Developmental biology · 2021
    Review
  6. A cookbook for DNase Hi-C.Epigenetics & chromatin · 2021
    Article
  7. Article
  8. Targeted DNase Hi-C.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  9. Methods for mapping 3D chromosome architecture.Nature reviews. Genetics · 2020
    Review
  10. Article
  11. Article
  12. Article
  13. Article
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

15 authors at 3 institutions in 1 country.

Wenxiu MaDepartment of Genome Sciences, University of Washington, USA.
Ferhat AyDepartment of Genome Sciences, University of Washington, USA.
Choli LeeDepartment of Genome Sciences, University of Washington, USA.
Gunhan GulsoyDepartment of Genome Sciences, University of Washington, USA.
Xinxian DengDepartment of Pathology, University of Washington, USA.
Savannah CookInstitute for Stem Cell and Regenerative Medicine, University of Washington, USA; Department of Comparative Medicine, University of Washington, USA.
Jennifer HessonInstitute for Stem Cell and Regenerative Medicine, University of Washington, USA; Department of Comparative Medicine, University of Washington, USA.
Christopher CavanaughInstitute for Stem Cell and Regenerative Medicine, University of Washington, USA; Department of Comparative Medicine, University of Washington, USA.
Carol B WareInstitute for Stem Cell and Regenerative Medicine, University of Washington, USA; Department of Comparative Medicine, University of Washington, USA.
Anton KrummDepartment of Radiation Oncology, University of Washington, USA.
Jay ShendureDepartment of Genome Sciences, University of Washington, USA; Howard Hughes Medical Institute, Seattle, WA 98195-8056, USA.
C Anthony BlauInstitute for Stem Cell and Regenerative Medicine, University of Washington, USA; Division of Hematology, Department of Medicine, University of Washington, USA.
Christine M DistecheDepartment of Pathology, University of Washington, USA.
William S NobleDepartment of Genome Sciences, University of Washington, USA. Electronic address: william-noble@uw.edu.
ZhiJun DuanInstitute for Stem Cell and Regenerative Medicine, University of Washington, USA; Division of Hematology, Department of Medicine, University of Washington, USA. Electronic address: zjduan@uw.edu.
University of Washington · USCalifornia Institute for Regenerative Medicine · USHoward Hughes Medical Institute · US

Funding

University of Washington Center for Nuclear Organization and FunctionU54DK107979 · NIDDK · UNIVERSITY OF WASHINGTON · PI NOBLE, WILLIAM STAFFORD · 2015 to 2019
$11.8M
Intellectual and Developmental Disabilities Research CenterU54HD083091 · NICHD · UNIVERSITY OF WASHINGTON · PI GURALNICK, MICHAEL J · 2014 to 2019
$7.9M
Howard Hughes Medical InstituteNICHD NIH HHS U54 HD083091NIDDK NIH HHS U54 DK107979
6 · The paper itself

Abstract

The folding and three-dimensional (3D) organization of chromatin in the nucleus critically impacts genome function. The past decade has witnessed rapid advances in genomic tools for delineating 3D genome architecture. Among them, chromosome conformation capture (3C)-based methods such as Hi-C are the most widely used techniques for mapping chromatin interactions. However, traditional Hi-C protocols rely on restriction enzymes (REs) to fragment chromatin and are therefore limited in resolution. We recently developed DNase Hi-C for mapping 3D genome organization, which uses DNase I for chromatin fragmentation. DNase Hi-C overcomes RE-related limitations associated with traditional Hi-C methods, leading to improved methodological resolution. Furthermore, combining this method with DNA capture technology provides a high-throughput approach (targeted DNase Hi-C) that allows for mapping fine-scale chromatin architecture at exceptionally high resolution. Hence, targeted DNase Hi-C will be valuable for delineating the physical landscapes of cis-regulatory networks that control gene expression and for characterizing phenotype-associated chromatin 3D signatures. Here, we provide a detailed description of method design and step-by-step working protocols for these two methods.

Indexed as

Cell Culture TechniquesCell NucleusChromatinChromosome MappingCross-Linking ReagentsDeoxyribonuclease IDNA Restriction EnzymesFormaldehydeGene LibraryHigh-Throughput Nucleotide SequencingImaging, Three-DimensionalMolecular ImagingTissue Culture TechniquesWhole Genome SequencingChromatinCross-Linking ReagentsDeoxyribonuclease IDNA Restriction EnzymesFormaldehydeChromatinChromosomeChromosome conformation capture (3C)DNase Hi-CHi-CThree-dimensional (3D) genome architecture

Identifiers

PMID29382556
PMCPMC5993575
OpenAlexW2950042474

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.