Abstract 3214: BART: An integrative bioinformatics toolkit and web server for functional transcription factor prediction

Author(s):  
Zhenjia Wang ◽  
Wenjing Ma ◽  
Yifan Zhang ◽  
Neal E. Magee ◽  
Yang Chen ◽  
...  
2008 ◽  
Vol 2008 ◽  
pp. 1-9 ◽  
Author(s):  
J. Sunil Rao ◽  
Suresh Karanam ◽  
Colleen D. McCabe ◽  
Carlos S. Moreno

Background. The computational identification of functional transcription factor binding sites (TFBSs) remains a major challenge of computational biology. Results. We have analyzed the conserved promoter sequences for the complete set of human RefSeq genes using our conserved transcription factor binding site (CONFAC) software. CONFAC identified 16296 human-mouse ortholog gene pairs, and of those pairs, 9107 genes contained conserved TFBS in the 3 kb proximal promoter and first intron. To attempt to predict in vivo occupancy of transcription factor binding sites, we developed a novel marginal effect isolator algorithm that builds upon Bayesian methods for multigroup TFBS filtering and predicted the in vivo occupancy of two transcription factors with an overall accuracy of 84%. Conclusion. Our analyses show that integration of chromatin immunoprecipitation data with conserved TFBS analysis can be used to generate accurate predictions of functional TFBS. They also show that TFBS cooccurrence can be used to predict transcription factor binding to promoters in vivo.


2015 ◽  
Vol 43 (W1) ◽  
pp. W283-W288 ◽  
Author(s):  
Mohamed Hamed ◽  
Christian Spaniol ◽  
Maryam Nazarieh ◽  
Volkhard Helms

2015 ◽  
Vol 44 (8) ◽  
pp. e72-e72 ◽  
Author(s):  
Stefan H. Lelieveld ◽  
Judith Schütte ◽  
Maurits J.J. Dijkstra ◽  
Punto Bawono ◽  
Sarah J. Kinston ◽  
...  

2013 ◽  
Vol 23 (8) ◽  
pp. 1319-1328 ◽  
Author(s):  
B. C. Haynes ◽  
E. J. Maier ◽  
M. H. Kramer ◽  
P. I. Wang ◽  
H. Brown ◽  
...  

2019 ◽  
Author(s):  
Timothy O’Connor ◽  
Charles E. Grant ◽  
Mikael Bodén ◽  
Timothy L. Bailey

AbstractMotivationIdentifying the genes regulated by a given transcription factor (its “target genes”) is a key step in developing a comprehensive understanding of gene regulation. Previously we developed a method for predicting the target genes of a transcription factor (TF) based solely on the correlation between a histone modification at the TF’s binding site and the expression of the gene across a set of tissues. That approach is limited to organisms for which extensive histone and expression data is available, and does not explicitly incorporate the genomic distance between the TF and the gene.ResultsWe present the T-Gene algorithm, which overcomes these limitations. T-Gene can be used to predict which genes are most likely to be regulated by a TF, and which of the TF’s binding sites are most likely involved in regulating particular genes. T-Gene calculates a novel score that combines distance and histone/expression correlation, and we show that this score accurately predicts when a regulatory element bound by a TF is in contact with a gene’s promoter, achieving median positive predictive value (PPV) above 50%. T-Gene is easy to use via its web server or as a command-line tool, and can also make accurate predictions (median PPV above 40%) based on distance alone when extensive histone/expression data is not available for the organism. T-Gene provides an estimate of the statistical significance of each of its predictions.AvailabilityThe T-Gene web server, source code, histone/expression data and genome annotation files are provided at http://[email protected]


2005 ◽  
Vol preprint (2006) ◽  
pp. e130
Author(s):  
Alan M. Moses ◽  
Daniel Pollard ◽  
David A Nix ◽  
Venky N. Iyer ◽  
Xiao-Yong Li ◽  
...  

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