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Single-nucleus RNA sequencing (snRNA-seq), where nuclear transcriptomes are a proxy to cellular transcriptomes, has been used to profile human brain. snRNA-seq is sensitive to tissue processing, tissue quality, postmortem interval time, and cellular debris. This protocol outlines steps for the isolation of high-quality nuclei from surgically resected human brain tissue followed by a sucrose gradient yielding neuronal and non-neuronal nuclei enabling unbiased analysis of various cell types. For complete details on the use and execution of this protocol, please refer to Ayhan et al. (2021).
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Fatma Ayhan
Batman University
Connor Douglas
Southwestern Medical Center
Bradley Lega
Neurological Surgery
SHILAP Revista de lepidopterología
STAR Protocols
The University of Texas Southwestern Medical Center
Southwestern Medical Center
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Ayhan et al. (Thu,) studied this question.
synapsesocial.com/papers/69df0821acbf09c32e61408a — DOI: https://doi.org/10.1016/j.xpro.2021.100844
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