H3K4me3 ChIP-seq of primary human keratinocytes after 6 hours of differentiation induction

To determine as a proxy transcriptional activation after induction of differentiation, we performed H3K4me3 ChIP-seq experiment of primary human keratinocytes that were treated with EGFR inhibitor AG1478 and BMP2/7 for 6 hours. H3K4me3 data of control and 6h AG1478 treated primary human keratinocytes

为将分化诱导后的转录激活情况作为替代检测指标，我们对经表皮生长因子受体（Epidermal Growth Factor Receptor，EGFR）抑制剂AG1478与骨形态发生蛋白2/7（Bone Morphogenetic Protein 2/7，BMP2/7）处理6小时的原代人角质形成细胞，开展了H3K4me3染色质免疫共沉淀测序（Chromatin Immunoprecipitation sequencing，ChIP-seq）实验。本数据集包含对照组以及经6小时AG1478处理的原代人角质形成细胞的H3K4me3测序数据。