E-GEOD-47753 - Transposition of native chromatin for fast and sensitive epigenomic profiling of open chromatin, DNA-binding proteins and nucleosome position

Released on 1 October 2013, last updated on 25 November 2013
Homo sapiens
Samples (13)
Protocols (3)
We describe an assay for transposase-accessible chromatin using sequencing (ATAC-seq), based on direct in vitro transposition of sequencing adaptors into native chromatin, as a rapid and sensitive method for integrative epigenomic analysis. ATAC-seq captures open chromatin sites using a simple two-step protocol with 500–50,000 cells and reveals the interplay between genomic locations of open chromatin, DNA-binding proteins, individual nucleosomes and chromatin compaction at nucleotide resolution. We discovered classes of DNA-binding factors that strictly avoided, could tolerate or tended to overlap with the nucleosome. Using ATAC-seq maps of human CD4+ T cells from a proband obtained on consecutive days, we demonstrated the feasibility of analyzing an individual’s epigenome on a timescale compatible with clinical decision-making. We examined chromatin structure using ATAC-seq in 2 cell types (GM12878 cell line, purified CD4+ T cells).
Experiment type
Howard Y Chang, Jason D Buenrostro, Lisa C Zaba, Paul G Giresi, William J Greenleaf
Exp. designProtocolsVariablesProcessedSeq. reads
Investigation descriptionE-GEOD-47753.idf.txt
Sample and data relationshipE-GEOD-47753.sdrf.txt
Additional data (1)E-GEOD-47753.additional.1.zip