Evidence map›Paper›PMID 17286865›Full record

ArticleBMC bioinformatics2007

WeederH: an algorithm for finding conserved regulatory motifs and regions in homologous sequences.

Giulio Pavesi, Federico Zambelli, Graziano Pesole

Abstract read
In one paragraph

Article in BMC bioinformatics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Maser: one-stop platform for NGS big data from analysis to visualization.Database : the journal of biological databases and curation · 2018
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Exhaustive search for over-represented DNA sequence motifs with CisFinder.DNA research : an international journal for rapid publication of reports on genes and genomes · 2009
    Article
  14. Promoter analysis: gene regulatory motif identification with A-GLAM.Methods in molecular biology (Clifton, N.J.) · 2009
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review of Different Sequence Motif Finding Algorithms.Avicenna journal of medical biotechnology
    Review
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.

Giulio PavesiDipartimento di Scienze Biomolecolari e Biotecnologie, University of Milan, Milan, Italy. giulio.pavesi@unimi.it
Federico Zambelli
Graziano Pesole

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis work addresses the problem of detecting conserved transcription factor binding sites and in general regulatory regions through the analysis of sequences from homologous genes, an approach that is becoming more and more widely used given the ever increasing amount of genomic data available.

resultsWe present an algorithm that identifies conserved transcription factor binding sites in a given sequence by comparing it to one or more homologs, adapting a framework we previously introduced for the discovery of sites in sequences from co-regulated genes. Differently from the most commonly used methods, the approach we present does not need or compute an alignment of the sequences investigated, nor resorts to descriptors of the binding specificity of known transcription factors. The main novel idea we introduce is a relative measure of conservation, assuming that true functional elements should present a higher level of conservation with respect to the rest of the sequence surrounding them. We present tests where we applied the algorithm to the identification of conserved annotated sites in homologous promoters, as well as in distal regions like enhancers.

conclusionResults of the tests show how the algorithm can provide fast and reliable predictions of conserved transcription factor binding sites regulating the transcription of a gene, with better performances than other available methods for the same task. We also show examples on how the algorithm can be successfully employed when promoter annotations of the genes investigated are missing, or when regulatory sites and regions are located far away from the genes.

Indexed as

AlgorithmsSequence Homology, Nucleic AcidBase SequenceBinding SitesChromosome MappingConserved SequenceMolecular Sequence DataProtein BindingRegulatory Sequences, Nucleic AcidSequence Analysis, DNASoftwareTranscription FactorsTranscription Factors

Identifiers

PMID17286865
PMCPMC1803799

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.