Evidence map›Paper›PMID 17576669›Full record

ArticleNucleic acids research2007

A new systematic computational approach to predicting target genes of transcription factors.

Xinbin Dai, Ji He, Xuechun Zhao

Abstract readValidation Study
In one paragraph

Article in Nucleic acids research, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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.

Xinbin DaiPlant Biology Division, the Samuel Robert Noble Foundation, Ardmore, OK 73401, USA.
Ji He
Xuechun Zhao

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identifying transcription factor target genes (TFTGs) is a vital step towards understanding regulatory mechanisms of gene expression. Methods for the de novo identification of TFTGs are generally based on screening for novel DNA binding sites. However, experimental screening of new binding sites is a technically challenging, laborious and time-consuming task, while computational methods still lack accuracy. We propose a novel systematic computational approach for predicting TFTGs directly on a genome scale. Utilizing gene co-expression data, we modeled the prediction problem as a 'yes' or 'no' classification task by converting biological sequences into novel reverse-complementary position-sensitive n-gram profiles and implemented the classifiers with support vector machines. Our approach does not necessarily predict new DNA binding sites, which other studies have shown to be difficult and inaccurate. We applied the proposed approach to predict auxin-response factor target genes from published Arabidopsis thaliana co-expression data and obtained satisfactory results. Using ten-fold cross validations, the area under curve value of the receiver operating characteristic reaches around 0.73.

Indexed as

Promoter Regions, GeneticAlgorithmsArabidopsisArtificial IntelligenceBinding SitesComputational BiologyGene ExpressionGenomicsTranscription FactorsTranscription Factors

Identifiers

PMID17576669
PMCPMC1935008

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.