80 series
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Accession Title Series type(s) Organism(s) Samples GDS Supplementary Contact Release date
Remove filtersFilter Remove filterGenome variation profiling by SNP array Remove filterCNCHP
GSE59244
Affymetrix SNP array data for 5q- myelodysplastic syndromes
4 Vera Adema Oct 07, 2014
GSE46594
The self-renewal of gastric cancer stem cells is regulated by a specific collaboration between the microenvironment and the genetic condition.
  • Genome variation profiling by SNP array
10 sujin Baek Dec 31, 2016
GSE46598
Integrated epigenomic analyses of enhancer as well as promoter regions in gastric cancer
37 sujin Baek Mar 29, 2016
GSE47914
Genomic instability of human embryonic stem cells in mechanic and enzymatic passaging culture
  • Genome variation profiling by SNP array
19 Qiang BAI Jun 01, 2015
GSE47917
Genome alterations in human pluripotent stem cells as very early events highly dependent on cell passaging conditions
30 Qiang BAI Jun 01, 2015
GSE21780
SNP arrays in matched diagnosis/remission samples of normal karyotype-acute myeloid leukemia
30 Vincenza Barresi Dec 31, 2010
GSE46969
Affymetrix SNP array data for 29 MCL cases
  • Genome variation profiling by SNP array
67 Sílvia Beà Nov 04, 2013
GSE108475
The REMBRANDT study – a large collection of genomic data from brain cancer patients [SNP]
  • Genome variation profiling by SNP array
1506 Krithika Bhuvaneshwar May 25, 2018
GSE108476
The REMBRANDT study – a large collection of genomic data from brain cancer patients
2056 Krithika Bhuvaneshwar May 25, 2018
GSE37977
SNP6.0 copy number analysis of eight diffuse large B-cell samples and one matched blood sample
  • Genome variation profiling by SNP array
9 Julie Støve Bødker Nov 26, 2012
GSE37979
Performance Comparison of the Affymetrix SNP6.0 and Cytogenetic 2.7M Whole-genome Microarrays in Complex Cancer Samples
  • Genome variation profiling by SNP array
18 Julie Støve Bødker Nov 26, 2012
GSE20564
Genotyping data from one patient with unexplained mental retardation and a deletion in 15q13
2 Michael Bonin Mar 05, 2011
GSE132453
Comorbidities - microcephaly, facial dysmorphia and epilepsy - increase the risk of the pathogenic CNV finding in patients with intellectual disability and autism
112 Zuzana Čapková Jun 11, 2019
GSE63630
The reversed evolution from multicellularity to unicellularity during carcinogenesis
12 Han Chen Nov 27, 2014
GSE29772
CNV analysis for Generation of isogenic pluripotent stem cells differing exclusively at two early onset Parkinson point mutations
  • Genome variation profiling by SNP array
6 Albert W Cheng Jul 26, 2011
GSE29774
Generation of isogenic pluripotent stem cells differing exclusively at two early onset Parkinson point mutations
18 Albert W Cheng Jul 26, 2011
GSE80460
SNP arrays in matched colorectal cancer and normal colonic mucosa.
  • Genome variation profiling by SNP array
97 Daniele F Condorelli Aug 31, 2018
GSE267025
SNP arrays in colorectal adenocarcinoma cell lines
  • Genome variation profiling by SNP array
3 Daniele F Condorelli Jun 05, 2024
GSE107507
The molecular basis of T-PLL is an actionable perturbation of TCL1/ATM- and epigenetically instructed damage responses [human SNP array]
  • Genome variation profiling by SNP array
113 Giuliano Crispatzu Nov 30, 2017
GSE107513
The molecular basis of T-PLL is an actionable perturbation of TCL1/ATM- and epigenetically instructed damage responses
276 Giuliano Crispatzu Nov 30, 2017