Difference between revisions of "Computational Regulatory Genomics"

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We have recently made significant progress in understanding the DNA sequence features which control cell-type specific mammalian enhancer activity by using kmer-based SVM machine learning approaches.  For details, see:
 
We have recently made significant progress in understanding the DNA sequence features which control cell-type specific mammalian enhancer activity by using kmer-based SVM machine learning approaches.  For details, see:
  
This work uses functional genomics DNase-seq, ChIP-seq, RNA-seq, and chromatin state data to computationally identify combinations of transcription factor binding sites which operate to define a set of cell-specific enhancers.  We are currently focused on:
+
* '''[http://www.horizonpress.com/genomeanalysis Mammalian Enhancer Prediction.]''' Lee D, Beer MA. 2014. Genome Analysis: Current Procedures and Applications. Horizon Press (in press)
1) improving this methodology by including more diverse constraints and features
+
 
2) predicting the impact of SNPs on enhancer activity (delta-SVM) and GWAS disease association
+
* '''[http://www.ncbi.nlm.nih.gov/pubmed/23861010 Robust k-mer Frequency Estimation Using Gapped k-mers.]''' Ghandi M, Mohammad-Noori M, and Beer MA. 2013. Journal of Mathematical Biology. (Epub ahead of print)
3) experimentally characterizing the predicted impact of regulatory element mutation in mammalian cells
+
 
4) systematically determining regulatory elements from ENCODE human and mouse data
+
* '''[http://www.ncbi.nlm.nih.gov/pubmed/23771147 kmer-SVM: a web server for identifying predictive regulatory sequence features in genomic datasets.]''' Fletez-Brant C*, Lee D*, McCallion AS and Beer MA. 2013. Nucleic Acids Research 41: W544–W556.
5) using the inferred regulatory code to assess common modes of regulatory element evolution and variation
+
 
 +
* '''[http://www.ncbi.nlm.nih.gov/pubmed/23019145 Integration of ChIP-seq and Machine Learning Reveals Enhancers and a Predictive Regulatory Sequence Vocabulary in Melanocytes.]''' Gorkin DU, Lee D, Reed X, Fletez-Brant C, Blessling SL, Loftus SK, Beer MA, Pavan WJ, and McCallion AS. 2012. Genome Research 22:2290-2301.
 +
 
 +
* '''[http://www.ncbi.nlm.nih.gov/pubmed/21875935 Discriminative prediction of mammalian enhancers from DNA sequence.]''' Lee D, Karchin R, and Beer MA. 2011. Genome Research 21:2167-2180.
 +
 
 +
This work uses functional genomics DNase-seq, ChIP-seq, RNA-seq, and chromatin state data to computationally identify combinations of transcription factor binding sites which operate to define the activity of a set of cell-type specific enhancers.  We are currently focused on:
 +
 
 +
* improving this methodology by including more diverse constraints and features
 +
* predicting the impact of SNPs on enhancer activity (delta-SVM) and GWAS disease association
 +
* experimentally characterizing the predicted impact of regulatory element mutation in mammalian cells
 +
* systematically determining regulatory elements from ENCODE human and mouse data
 +
* using the inferred regulatory code to assess common modes of regulatory element evolution and variation
 
</h3>
 
</h3>
  
 
<h3>[[Lab Members]]</h3>
 
<h3>[[Lab Members]]</h3>
 
<h3>[[Publications]]</h3>
 
<h3>[[Publications]]</h3>

Revision as of 23:47, 1 December 2013

Welcome to the Beer Lab!

Beer lab plate art.jpg

Research Interests:

The ultimate goal of our research is to understand how genomic DNA sequence specifies gene regulation.

We have recently made significant progress in understanding the DNA sequence features which control cell-type specific mammalian enhancer activity by using kmer-based SVM machine learning approaches. For details, see:

This work uses functional genomics DNase-seq, ChIP-seq, RNA-seq, and chromatin state data to computationally identify combinations of transcription factor binding sites which operate to define the activity of a set of cell-type specific enhancers. We are currently focused on:

  • improving this methodology by including more diverse constraints and features
  • predicting the impact of SNPs on enhancer activity (delta-SVM) and GWAS disease association
  • experimentally characterizing the predicted impact of regulatory element mutation in mammalian cells
  • systematically determining regulatory elements from ENCODE human and mouse data
  • using the inferred regulatory code to assess common modes of regulatory element evolution and variation

Lab Members

Publications