PRISM predicts interactions between transcription factors and their regulated genes from binding motifs.

Understanding vertebrate development requires unraveling the cis-regulatory architecture of gene regulation. PRISM provides accurate genome-wide computational predictions of transcription factor binding sites for the human and mouse genomes, and integrates the predictions with GREAT to provide functional biological context. Together, accurate computational binding site prediction and GREAT produce for each transcription factor: 1. putative binding sites, 2. putative target genes, 3. putative biological roles of the transcription factor, and 4. putative cis-regulatory elements through which the factor regulates each target in each functional role.


News

  • June 2022: We updated our computationally predicted PRISM conserved transcription factor binding sites (TFBSs) for the human (Homo sapiens GRCh38 and GRCh37) and mouse (Mus musculus GRCm38 and NCBIM37) genomes as a part of our recent WhichTF study. The latest PRISM prediction tracks are available at figshare.
  • February 2013: PRISM is published as a resource article in Genome Research.

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Species Assembly

(UCSC hg18, Mar 2006)
(UCSC mm9, Jul 2007)

Perspective

Transcription factor regulator
(e.g. "HOXA1")
Biological role
(e.g. "DNA modification")
Target gene
(e.g. "fox")
Target genomic region
(e.g. "chr1:2-30,000,000")