Evidence map›Paper›PMID 28591841›Full record

ArticleNucleic acids research2017

RSAT matrix-clustering: dynamic exploration and redundancy reduction of transcription factor binding motif collections.

Jaime Abraham Castro-Mondragon, Sébastien Jaeger, Denis Thieffry, Morgane Thomas-Chollier, Jacques van Helden

Abstract read
In one paragraph

Article in Nucleic acids research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing 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

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3 · Its place in the literature

Who cites it

84 citing papers in PubMed.

  1. Article
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  3. AmalgaMo: flexible DNA motif merging.Bioinformatics advances · 2026
    Article
  4. The Binding Landscape of an Essential Nuclear Hormone Receptor inbioRxiv : the preprint server for biology · 2025
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24 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

5 authors.

Jaime Abraham Castro-MondragonAix Marseille Univ, INSERM, TAGC, Theory and Approaches of Genomic Complexity, UMR_S 1090, Marseille, France.
Sébastien JaegerAix Marseille Univ, CNRS, INSERM, CIML, Marseille, France.
Denis ThieffryIBENS, Département de Biologie, Ecole Normale Supérieure, CNRS, Inserm, PSL Research University, F-75005 Paris, France.
Morgane Thomas-ChollierIBENS, Département de Biologie, Ecole Normale Supérieure, CNRS, Inserm, PSL Research University, F-75005 Paris, France.
Jacques van HeldenAix Marseille Univ, INSERM, TAGC, Theory and Approaches of Genomic Complexity, UMR_S 1090, Marseille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transcription factor (TF) databases contain multitudes of binding motifs (TFBMs) from various sources, from which non-redundant collections are derived by manual curation. The advent of high-throughput methods stimulated the production of novel collections with increasing numbers of motifs. Meta-databases, built by merging these collections, contain redundant versions, because available tools are not suited to automatically identify and explore biologically relevant clusters among thousands of motifs. Motif discovery from genome-scale data sets (e.g. ChIP-seq) also produces redundant motifs, hampering the interpretation of results. We present matrix-clustering, a versatile tool that clusters similar TFBMs into multiple trees, and automatically creates non-redundant TFBM collections. A feature unique to matrix-clustering is its dynamic visualisation of aligned TFBMs, and its capability to simultaneously treat multiple collections from various sources. We demonstrate that matrix-clustering considerably simplifies the interpretation of combined results from multiple motif discovery tools, and highlights biologically relevant variations of similar motifs. We also ran a large-scale application to cluster ∼11 000 motifs from 24 entire databases, showing that matrix-clustering correctly groups motifs belonging to the same TF families, and drastically reduced motif redundancy. matrix-clustering is integrated within the RSAT suite (http://rsat.eu/), accessible through a user-friendly web interface or command-line for its integration in pipelines.

Indexed as

AlgorithmsAmino Acid MotifsAmino Acid SequenceAnimalsBinding SitesChromatin ImmunoprecipitationCluster AnalysisDatabases, ProteinHigh-Throughput Nucleotide SequencingHumansMiceProtein BindingSequence Analysis, ProteinTranscription FactorsTranscription Factors

Identifiers

PMID28591841
PMCPMC5737723

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LicenceCC BY-NC
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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.