Genomic Analysis of Epigenetic Regulation

We leverage the strength of ATAC-seq to profile open chromatin landscape with as few as 50 thousand cells, and have

optimized an "on-plate" protocol for adherent cells without the need of trypsinization. We further integrate the data analysis 

of ATAC-seq, ChIP-seq, and RNA-seq to elucidate gene regulation mechanism. 


Using 3'READS+ (3' Region Extraction and Deep Sequencing plus), we have recently mapped the transcriptome-wide termination sites in primary human keratinocytes. In particular, 2739 of these termination sites are mapped to introns! We are currently characterizing the function and regulation of these intronic sites. 

We uncover novel protein-protein interactions, both stable and transient associations, via both conventional affinity purification as well as the BirA purification system. We are also interested in deciphering the roles of post-translational modifications such as phosphorylation and methylation. 

Proteomic Identification of Interactome and Modifications

TAP

Rapid Genetic Characterization in Intact Human Tissue

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Our characterization of gene function within 3-dimensional organotypic human tissue can be achieved in less than a week. We have further developed a "Stem Cell Competition Assay" to label and track living human cells in vivo by grafting self-renewing human epidermal tissue. 

​​Organotypic Human Tissue Regeneration (~ 1 week)

Bao Lab         

Gene Regulation of Stem Cell Maintenance and Differentiation 

Stem Cell Competition Assay in vivo

Email: xbchromatin@gmail.com