Cutting down steroid biosynthesis through SIRT6 induced H3K56ac deacetylation Fuels the osteogenic commitment of MSCs (ChIP-Seq)
ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 10 samples
- What it is
- ChIP-seq / ATAC-seq (genome binding and open chromatin)Where proteins bind the genome, or which regions are open and active.
- Organism
- Homo sapiens (human)
- Samples
- 10 samples: 10 samples, each with a distinct title — no replicated groupsGroups are read from the sample names, not from the paper. Check the list below.
- Data you can get
- A processed table (series matrix) and supplementary files from NCBI; the raw sequencing reads from ENA. Which of these hold counts depends on the study, so check the file list.
Direct links to NCBI and ENA, no account and no request form. Pick by what you want to do: take the small processed table to look, the supplementary files to re-analyse, or the original raw data to start over.
Processed table
The series matrix: one table of values per sample as the submitters processed it. The smallest download, and it opens in Excel or R. Start here to see what the data look like.
Supplementary files
The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE232534_RAW.tar (it can run to tens of gigabytes).
Raw sequencing reads
The original FASTQ files, straight from the sequencer, held at ENA. Large, and you align them yourself, so only choose this if you need to re-process the study from scratch.
What the files usually look like: Look for peak files (.bed, .narrowPeak) and signal tracks (.bigWig) among the supplementary files; the raw reads are on ENA.
Also filed as BioProject PRJNA972689 and SRA study SRP437708. Searching any of these in the dataset finder brings you back here.
Any grouping that defines a comparison lives in the sample characteristics, which GEO records separately from the titles.
How we read this: Read from 10 sample titles: 10 distinct titles with little repetition. These groups are guessed from the sample names, not taken from the paper, so check them against the sample list below before relying on them.
- GSM7349952 HDPCs, IgG, Millipore
- GSM7349953 HDPCs, cross-linked and sonicated only Input
- GSM7349954 HDPC, anti-H3K9ac, abcam, bio rep1 K9ac8_1
- GSM7349955 HDPC, anti-H3K9ac, abcam, bio rep2 K9ac8_2
- GSM7349956 HDPC, anti-H3K9ac, abcam, bio rep1 K9acD_1
- GSM7349957 HDPC, anti-H3K9ac, abcam, bio rep2 K9acD_2
- GSM7349958 HDPC, anti-H3K56ac, abcam, bio rep1 K56ac8_1
- GSM7349959 HDPC, anti-H3K56ac, abcam, bio rep2 K56ac8_2
- GSM7349960 HDPC, anti-H3K56ac, abcam, bio rep1 K56acD_1
- GSM7349961 HDPC, anti-H3K56ac, abcam, bio rep2 K56acD_2
- GSE232537 Cutting down steroid biosynthesis through SIRT6 induced H3K56ac deacetylation Fuels the osteogenic commitment of MSCs 22 samples shares h3k56ac, sirt6, deacetylation, biosynthesis, osteogenic, commitment, cutting
- GSE232535 Cutting down steroid biosynthesis through SIRT6 induced H3K56ac deacetylation Fuels the osteogenic commitment of MSCs (RNA-Seq) 12 samples shares h3k56ac, sirt6, deacetylation, biosynthesis, osteogenic, commitment, cutting
- GSE315635 ChIP-Seq analysis of SIRT6 and KDM5C in pancreatic cancer cell line 3 samples shares sirt6, chip-seq
- GSE270024 RCOR2 downregulates CIITA via HDAC1-mediated histone deacetylation in cancer cells [ChIP-seq] 12 samples shares deacetylation, chip-seq
- GSE261903 SIRT6-dependent functional switch via K494 modifications of RE-1 Silencing Transcription factor [REST_experiment_2] 30 samples shares sirt6
- GSE261902 SIRT6-dependent functional switch via K494 modifications of RE-1 Silencing Transcription factor [REST_experiment_1] 24 samples shares sirt6
- GSE295913 Genomic Profiling of Sirt6 binding sites in the neuroblastoma cell line ShSy-5y under normal culture conditions. 7 samples shares sirt6
- GSE296003 Histone 3 lysine 56 acetylation (H3K56ac) regulates extrachromosomal DNA (ecDNA) hub biogenesis 6 samples shares h3k56ac
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.