Evidence map›Paper›PMID 22198700›Full record

ArticleNature biotechnology2011

Genome architectures revealed by tethered chromosome conformation capture and population-based modeling.

Reza Kalhor, Harianto Tjong, Nimanthi Jayathilaka, Frank Alber, Lin Chen

Abstract read
In one paragraph

Article in Nature biotechnology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 336 papers.

0numbers the graph read from it
0cells of the map it votes in
336citing papers in PubMed
17.3field-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

336 citing papers in PubMed, 569 citations in OpenAlex.

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  7. Advancements and future directions in single-cell Hi-C based 3D chromatin modeling.Computational and structural biotechnology journal · 2024
    Review
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276 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Reza KalhorMolecular and Computational Biology, Department of Biological Sciences, University of Southern California, Los Angeles, California, USA.
Harianto Tjong
Nimanthi Jayathilaka
Frank Alber
Lin Chen
University of Southern California · US

Funding

NEW TOOLS FOR EXPLORING THE DYNAMIC INTERACTOME(RMI)U54RR022220 · NCRR · ROCKEFELLER UNIVERSITY · PI ROUT, MICHAEL P · 2005 to 2011
$19.3M
Structural and Functional Versatility of NFATR01GM064642 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHEN, LIN · 2005 to 2014
$2.5M
Computational Methods Towards the Spatio-Temporal Organization of the ProteomeR01GM096089 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ALBER, FRANK · 2011 to 2015
$1.6M
Structure and Function of the FOXP Family of Transcription FactorsR01GM077320 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHEN, LIN · 2006 to 2009
$959k
NCRR NIH HHS RR022220NCRR NIH HHS U54 RR022220NIGMS NIH HHS GM064642NIGMS NIH HHS GM077320NIGMS NIH HHS GM096089NIGMS NIH HHS R01 GM064642NIGMS NIH HHS R01 GM077320NIGMS NIH HHS R01 GM096089
6 · The paper itself

Abstract

We describe tethered conformation capture (TCC), a method for genome-wide mapping of chromatin interactions. By performing ligations on solid substrates rather than in solution, TCC substantially enhances the signal-to-noise ratio, thereby facilitating a detailed analysis of interactions within and between chromosomes. We identified a group of regions in each chromosome in human cells that account for the majority of interchromosomal interactions. These regions are marked by high transcriptional activity, suggesting that their interactions are mediated by transcriptional machinery. Each of these regions interacts with numerous other such regions throughout the genome in an indiscriminate fashion, partly driven by the accessibility of the partners. As a different combination of interactions is likely present in different cells, we developed a computational method to translate the TCC data into physical chromatin contacts in a population of three-dimensional genome structures. Statistical analysis of the resulting population demonstrates that the indiscriminate properties of interchromosomal interactions are consistent with the well-known architectural features of the human genome.

Indexed as

Genome, HumanTranscription, GeneticCell LineChromatinChromatin Assembly and DisassemblyChromosomes, HumanHumansIn Situ Hybridization, FluorescenceModels, MolecularMolecular ConformationSignal-To-Noise RatioChromatin

Identifiers

PMID22198700
PMCPMC3782096
OpenAlexW2170696599

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.