Evidence map›Paper›PMID 21152003›Full record

ArticlePLoS computational biology2010

Assessing computational methods of cis-regulatory module prediction.

Jing Su, Sarah A Teichmann, Thomas A Down

Abstract readComparative Study
In one paragraph

Article in PLoS computational biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Article
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  3. Review
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  5. regCNN: identifyingComputational and structural biotechnology journal · 2022
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  6. Review
  7. Review
  8. Article
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  19. GAMI-CRM: Using de novo motif inference to detect cis-regulatory modules.Proceedings of the ... Congress on Evolutionary Computation. Congress on Evolutionary Computation · 2014
    Article
  20. 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.

Jing SuMRC Laboratory of Molecular Biology, Cambridge, United Kingdom.
Sarah A Teichmann
Thomas A Down

Funding

Medical Research Council MC_U105161047Wellcome TrustWellcome Trust 083563
6 · The paper itself

Abstract

Computational methods attempting to identify instances of cis-regulatory modules (CRMs) in the genome face a challenging problem of searching for potentially interacting transcription factor binding sites while knowledge of the specific interactions involved remains limited. Without a comprehensive comparison of their performance, the reliability and accuracy of these tools remains unclear. Faced with a large number of different tools that address this problem, we summarized and categorized them based on search strategy and input data requirements. Twelve representative methods were chosen and applied to predict CRMs from the Drosophila CRM database REDfly, and across the human ENCODE regions. Our results show that the optimal choice of method varies depending on species and composition of the sequences in question. When discriminating CRMs from non-coding regions, those methods considering evolutionary conservation have a stronger predictive power than methods designed to be run on a single genome. Different CRM representations and search strategies rely on different CRM properties, and different methods can complement one another. For example, some favour homotypical clusters of binding sites, while others perform best on short CRMs. Furthermore, most methods appear to be sensitive to the composition and structure of the genome to which they are applied. We analyze the principal features that distinguish the methods that performed well, identify weaknesses leading to poor performance, and provide a guide for users. We also propose key considerations for the development and evaluation of future CRM-prediction methods.

Indexed as

AlgorithmsModels, GeneticAnimalsArea Under CurveCluster AnalysisComputational BiologyDatabases, GeneticDrosophilaGenome, HumanGenome, InsectHumansPhylogenyRegulatory Elements, TranscriptionalROC CurveTranscription FactorsTranscription Factors

Identifiers

PMID21152003
PMCPMC2996316

What OpenQuestion holds

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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.