Dissecting developmental disorders caused by CTCF mutation at R567 [Hi-C]. Dissecting developmental disorders caused by CTCF mutation at R567 [Hi-C]
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下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA886690
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资源简介：
In this study, we performed BL-Hi-C experiments to investigate the influence of CTCF mutation on higher-order chromatin structures. Overall design: BL-Hi-C experiments were performed using wild-type and Ctcf homozygous mutated tissues from E18.5 mouse embryo.
创建时间：
2022-10-03
