Complete loss of H3K9 methylation dissolves mouse heterochromatin organization [RNA-seq 2]
收藏NIAID Data Ecosystem2026-03-12 收录
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE169636
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资源简介：
Establishment and characterization of mouse embryonic fibroblasts deficient for 6 H3K9 lysine methyltranswferases (KMT) RNA-seq of MEFs with following genotypes: wild type, Suv39h1/Suv39h2 KO, and G9a/Glp KO
创建时间：
2021-08-18
