Cohesin mutations suppress HLA class II gene expression to promote immune evasion during the progression to acute leukemia in children with Down syndrome
ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 180 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
- 180 samples: 180 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 GSE314941_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 PRJNA1393147 and SRA study SRP657765. 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 180 sample titles: 180 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.
- GSM9416399 2351914_CMY_ATAC_1
- GSM9416400 2351915_CMY_ATAC_2
- GSM9416401 2351916_CMY_ATAC_3
- GSM9416402 2351920_CMY_2B10_ATAC_1
- GSM9416403 2351921_CMY_2B10_ATAC_2
- GSM9416404 2351922_CMY_2B10_ATAC_3
- GSM9416405 2351923_CMY_3D11_ATAC_1
- GSM9416406 2351924_CMY_3D11_ATAC_2
- GSM9416407 2351925_CMY_3D11_ATAC_3
- GSM9416408 CMK_STAG2_R305X_Het_project.Miller-Plate55-F01-AAATACGCAG-GCATCA
- GSM9416409 CMK_STAG2_R305X_Het_project.Miller-Plate55-F03-CTCGGTACAC-GCATCA
- GSM9416410 CMK_STAG2_R305X_Het_project.Miller-Plate55-F07-CTCTAGAATG-GCATCA
- GSM9416411 CMY_CIITA_KO.Miller-Plate106-D01-GTCAGAAGGT-CTAGTC
- GSM9416412 CMY_CIITA_KO.Miller-Plate106-D02-TGAAATATAC-CTAGTC
- GSM9416413 CMY_CIITA_KO.Miller-Plate106-D03-CTCAACTGAG-CTAGTC
- GSM9416414 CMY_CIITA_KO.Miller-Plate106-D04-CGACATGATA-CTAGTC
- GSM9416415 CMY_CIITA_KO.Miller-Plate106-D05-TGCAAATTCA-CTAGTC
- GSM9416416 CMY_CIITA_KO.Miller-Plate106-D06-GTAATGTTTG-CTAGTC
- GSM9416417 CMY_CIITA_KO.Miller-Plate106-D07-TCAATATGAT-CTAGTC
- GSM9416418 CMY_CIITA_KO.Miller-Plate106-D08-GGGCAAGGTT-CTAGTC
- GSM9416419 CMY_CIITA_KO.Miller-Plate106-D09-AAGTTCTTGA-CTAGTC
- GSM9416420 CMY_CIITA_KO.Miller-Plate106-D10-ATCGATCACG-CTAGTC
- GSM9416421 CMY_CIITA_KO.Miller-Plate106-D11-ATTTCTTTAA-CTAGTC
- GSM9416422 CMY_CIITA_KO.Miller-Plate106-D12-GCCTTGCCAT-CTAGTC
- GSM9416423 CMY_CIITA_KO.Miller-Plate106-E01-TCTTGGCTAA-CTAGTC
- GSM9416424 CMY_CIITA_KO.Miller-Plate106-E02-ACTGCTTTCT-CTAGTC
- GSM9416425 CMY_CIITA_KO.Miller-Plate106-E03-TCCTTTCAGG-CTAGTC
- GSM9416426 CMY_CIITA_KO.Miller-Plate106-E04-CGCATGGTTG-CTAGTC
- GSM9416427 CMY_CIITA_KO.Miller-Plate106-E05-AGTGATGACC-CTAGTC
- GSM9416428 CMY_CIITA_KO.Miller-Plate106-E06-ATCCTCTCCT-CTAGTC
- GSM9416429 CMY_CIITA_KO.Miller-Plate106-E07-AACCTCGAGG-CTAGTC
- GSM9416430 CMY_CIITA_KO.Miller-Plate106-E08-CAGTCTTAAC-CTAGTC
- GSM9416431 CMY_CIITA_KO.Miller-Plate106-E09-ACCGACTCAC-CTAGTC
- GSM9416432 CMY_CIITA_KO.Miller-Plate106-E10-GCGCTGTTGT-CTAGTC
- GSM9416433 CMY_CIITA_KO.Miller-Plate106-E11-AGCGCGCTTT-CTAGTC
- GSM9416434 CMY_CIITA_KO.Miller-Plate106-E12-CCATGGTAGT-CTAGTC
- GSM9416435 CMY_CIITA_KO.Miller-Plate106-F01-CCCGCAACAT-CTAGTC
- GSM9416436 CMY_CIITA_KO.Miller-Plate106-F02-CAGTCCTGGG-CTAGTC
- GSM9416437 CMY_CIITA_KO.Miller-Plate106-F03-TCGCTAAGTG-CTAGTC
- GSM9416438 CMY_PPP1R12C_KO.Miller-Plate106-A01-ATAGAGCCAG-CTAGTC
+ 140 more — browse all 180 samples with per-sample file links →
- GSE268035 STAG2 Mutations Reshape the Cohesin-Structured Spatial Chromatin Architecture to Drive Gene Regulation in Acute myeloid Leukemia 541 samples shares mutations, leukemia, cohesin
- GSE270787 ZIC2 and ZIC3 promote SWI/SNF recruitment to safeguard progression towards human primed pluripotency 205 samples shares progression, promote
- GSE180791 Proteogenomic characterization reveals that lipid droplet formation promotes esophageal squamous cell cancer progression 102 samples shares progression, promote
- GSE234558 Tracking rare single donor and recipient immune and leukemia cells after allogeneic hematopoietic cell transplantation using mitochondrial DNA mutations 85 samples shares mutations, leukemia
- GSE240497 Activation of a nongenetic AHR-ELMSAN1 axis optimizes BET-targeting therapy and suppresses leukemia stem cells in preclinical models 66 samples shares suppress, leukemia
- GSE234552 Tracking of donor and recipient immune and leukemia phenotypes after allogeneic stem cell transplantation using mitochondrial DNA mutations. [ASAP-Seq 2] 30 samples shares mutations, leukemia
- GSE296187 Interleukin-23 promotes a pro-inflammatory Th17 cell state by stabilizing RORγt and suppressing glucocorticoid receptor activity I 28 samples shares suppress, promote
- GSE234555 Tracking of donor and recipient immune and leukemia phenotypes after allogeneic stem cell transplantation using mitochondrial DNA mutations. [ASAP-Seq 3] 14 samples shares mutations, leukemia
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.