| Literature DB >> 35478247 |
Fiorella C Grandi1,2,3, Hailey Modi1,2,3, Lucas Kampman1,2,3, M Ryan Corces4,5,6.
Abstract
The assay for transposase-accessible chromatin using sequencing (ATAC-seq) provides a simple and scalable way to detect the unique chromatin landscape associated with a cell type and how it may be altered by perturbation or disease. ATAC-seq requires a relatively small number of input cells and does not require a priori knowledge of the epigenetic marks or transcription factors governing the dynamics of the system. Here we describe an updated and optimized protocol for ATAC-seq, called Omni-ATAC, that is applicable across a broad range of cell and tissue types. The ATAC-seq workflow has five main steps: sample preparation, transposition, library preparation, sequencing and data analysis. This protocol details the steps to generate and sequence ATAC-seq libraries, with recommendations for sample preparation and downstream bioinformatic analysis. ATAC-seq libraries for roughly 12 samples can be generated in 10 h by someone familiar with basic molecular biology, and downstream sequencing analysis can be implemented using benchmarked pipelines by someone with basic bioinformatics skills and with access to a high-performance computing environment.Entities:
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Year: 2022 PMID: 35478247 PMCID: PMC9189070 DOI: 10.1038/s41596-022-00692-9
Source DB: PubMed Journal: Nat Protoc ISSN: 1750-2799 Impact factor: 17.021