Human promoter genomic composition demonstrates non-random groupings that reflect general cellular function

Markey C McNutt¹^,2 , Ron Tongbai¹ , Wenwu Cui¹ , Irene Collins¹ , Wendy J Freebern¹^,3 , Idalia Montano¹ , Cynthia M Haggerty¹ , GVR Chandramouli and Kevin Gardner¹

¹The Advanced Technology Center, Laboratory of Receptor Biology and Gene Expression, National Cancer Institute, Bethesda, Maryland 20892-4605, USA

²The University of Texas Southwestern Medical Center at Dallas, TX, USA

³Bristol-Myers Squibb, Syracuse, NY, USA

author email corresponding author email

BMC Bioinformatics 2005, 6:259doi:10.1186/1471-2105-6-259


Published:	18 October 2005

Additional files

Additional file 1:

Supplemental Table 2, ontology terms associated with the 4 clusters in Figure 2

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Additional file 2:

Supplemental Table 3, representative genes from Clusters one, six and thirteen

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