Dissecting developmental disorders caused by CTCF mutation at R567 [SPARC-seq]
Direct links to NCBI, no account and no request form: the whole study as GSE214691_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 2 samples.
Also filed as BioProject PRJNA886686. Searching any of these in the dataset finder brings you back here.
The sample list for this study is not cached yet. Press Sort into groups and it will be fetched from NCBI.
+ 2 more — browse all 2 samples with per-sample file links →
- GSE72539 CTCF binding polarity determines chromatin looping [4C] 504 samples
- GSE301663 T cell-intrinsic cGAS-CTCF regulation maintains regulatory T cell development and function [Hi-C] 8 samples
- GSE247756 RNASeq, multiome, and genomic profiling of hematopoietic progenitors and B cells from mice with a point mutation in MYC [Multiome] 8 samples
- GSE255858 O-GlcNAcylation of CTCF regulates 3D chromatin structure [HiC] 6 samples
- GSE269224 Hoxblinc lncRNA reprograms CTCF-independent TADs to drive leukemic transcription and HSC dysregulation in NUP98 fusion transformed leukemia [ChIRP-seq] 6 samples
- GSE269218 Hoxblinc lncRNA reprograms CTCF-independent TADs to drive leukemic transcription and HSC dysregulation in NUP98 fusion transformed leukemia [Hi-C] 5 samples
- GSE255407 Single cell approaches define two mammalian oligodendrocyte precursor cell populations and their evolution over developmental time [Xenium In Situ Gene Expression] 3 samples
- GSE283303 Hoxblinc lncRNA reprograms CTCF-independent TADs to drive leukemic transcription and HSC dysregulation in NUP98 fusion transformed leukemia [CTCF-HiChIP-seq] 2 samples
Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.