Evidence map›Paper›PMID 39237524›Full record

ArticleNature communications2024

Spectral-based detection of chromatin loops in multiplexed super-resolution FISH data.

Michaël Liefsoens, Timothy Földes, Maria Barbi

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. The Biological Function of Genome Organization.International journal of molecular sciences · 2025
    Review
  3. 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

3 authors.

Michaël LiefsoensDepartment of Mathematics, KU Leuven, Celestijnenlaan 200B, 3001, Leuven, Belgium. michael.liefsoens@kuleuven.be.ORCID 0009-0004-9965-1002
Timothy FöldesLPTMC, Sorbonne Université, CNRS, F-75005, Paris, France. foldes@mit.edu.
Maria BarbiLPTMC, Sorbonne Université, CNRS, F-75005, Paris, France.ORCID 0000-0003-1977-6880

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-19-CE45-0016Fonds Wetenschappelijk Onderzoek (Research Foundation Flanders) 11PG324N
6 · The paper itself

Abstract

Involved in mitotic condensation, interaction of transcriptional regulatory elements and isolation of structural domains, loop formation has become a paradigm in the deciphering of chromatin architecture and its functional role. Despite the emergence of increasingly powerful genome visualization techniques, the high variability in cell populations and the randomness of conformations still make loop detection a challenge. We introduce an approach for determining the presence and frequency of loops in a collection of experimental conformations obtained by multiplexed super-resolution imaging. Based on a spectral approach, in conjunction with neural networks, this method offers a powerful tool to detect loops in large experimental data sets, both at the population and single-cell levels. The method's performance is confirmed on experimental FISH data where Hi-C and other loop detection results are available. The method is then applied to recently published experimental data, where it provides a detailed and statistically quantified description of the global architecture of the chromosomal region under study.

Indexed as

ChromatinIn Situ Hybridization, FluorescenceAnimalsChromosomesHumansNeural Networks, ComputerNucleic Acid ConformationChromatin

Identifiers

PMID39237524
PMCPMC11377450

What OpenQuestion holds

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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.