GEM

From SEQwiki
Jump to: navigation, search

Application data

Created by Yuchun Guo, Shaun Mahony & David K Gifford
Biological application domain(s) ChIP-seq
Principal bioinformatics method(s) Peak calling, Sequence motif discovery
Technology Illumina HiSeq, Illumina Solexa
Created at Massachusetts Institute of Technology (MIT)
Maintained? Yes
Input format(s) BED, SAM, BAM, Bowtie, ELAND
Software features probabilistic mixture model, motif prior, multi-threading
Programming language(s) Java
Licence Commercial, Freeware
Operating system(s) Cross-Platform

Summary: GEM is a java software tool to analyze transcription factor binding ChIP-seq/ChIP-exo data. It predicts binding events, performs de novo motif discovery and use the motif to improve the binding event calling. It calls binding events right at (or very close to ) the motif positions, deconvolves closely spaced homotypic binding events and accurately discovers binding motifs.

"Error: no local variable "counter" was set." is not a number.

Description

GEM is a software tool to study protein-DNA interaction using ChIP-seq/ChIP-exo data. GEM links binding event discovery and motif discovery with positional priors in the context of a generative probabilistic model of ChIP data and genome sequence, resolves ChIP data into explanatory motifs and binding events at unsurpassed spatial resolution .

GEM has following features:

  • Exceptionally high spatial resolution on binding event prediction (aka peak calling)
  • Highly accurate de novo motif discovery
  • Resolve closely spaced (less than 500bp) homotypic events that appear as a single cluster of reads
  • Enable analysis of spatial binding constraints of multiple transcription factors, for detecting TF dimer binding sites, enhanceosomes, etc.






Links


References

  1. . 2012. PLoS Comput Biol


To add a reference for GEM, enter the PubMed ID in the field below and click 'Add'.

 


Search for "GEM" in the SEQanswers forum / BioStar or:

Web Search Wiki Sites Scientific