| Literature DB >> 35755130 |
Zechuan Shi1, Sudeshna Das1, Samuel Morabito2, Emily Miyoshi1, Vivek Swarup3.
Abstract
Single-nucleus ATAC sequencing (snATAC-seq) employs a hyperactive Tn5 transposase to gain precise information about the cis-regulatory elements in specific cell types. However, the standard protocol of snATAC-seq is not optimized for all tissues, including the brain. Here, we present a modified protocol for single-nuclei isolation from postmortem frozen human brain tissue, followed by snATAC-seq library preparation and sequencing. We also describe an integrated bioinformatics analysis pipeline using an R package (ArchRtoSignac) to robustly analyze snATAC-seq data. For complete details on the use and execution of this protocol, please refer to Morabito et al. (2021).Entities:
Keywords: Bioinformatics; Genomics; Health Sciences; Neuroscience; Sequence analysis; Sequencing
Mesh:
Substances:
Year: 2022 PMID: 35755130 PMCID: PMC9218237 DOI: 10.1016/j.xpro.2022.101491
Source DB: PubMed Journal: STAR Protoc ISSN: 2666-1667