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Links from GEO DataSets

Items: 20

1.

human medulloblastoma

(Submitter supplied) Whole-genome screening of DNA-copy number changes by array-based or matrix comparative genomic hybridization (matrix-CGH). Tumor DNA was hybridized against a single standard reference DNA-pool of the opposite sex than the patient. Every experiment was performed as dye-swap. Keywords: repeat sample
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL1432
94 Samples
Download data
Series
Accession:
GSE2139
ID:
200002139
2.

Array-CGH screening of medulloblastoma

(Submitter supplied) DNA copy-number profiling of 80 primary medulloblastomas of different histologies Keywords: Genetic modification
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL5685
80 Samples
Download data: GPR
Series
Accession:
GSE8634
ID:
200008634
3.

Human ependymomas.

(Submitter supplied) Whole-genome screening of DNA-copy number changes by array-based or matrix comparative genomic hybridization (matrix-CGH). Keywords: Repeat sample.
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL2920
68 Samples
Download data
Series
Accession:
GSE3435
ID:
200003435
4.

DKFZ Homo sapiens 6k-array, version 3/4, upgrade

(Submitter supplied) Whole-genome BAC-array. Isolated BAC-DNA was amplified by two-step DOP-PCR. PCR products were dissolved in 3xSSC, 1.5M betaine and spotted as triplicates on epoxysilane-coated slides.
Organism:
Homo sapiens
1 Series
68 Samples
Download data
Platform
Accession:
GPL2920
ID:
100002920
5.

Integrative Genomic Analysis of Medulloblastoma Identifies a Molecular Subgroup That Drives Poor Clinical Outcome [DNA copy number]

(Submitter supplied) Medulloblastomas are heterogeneous tumors that collectively represent the most common malignant brain tumor in children. To understand the molecular characteristics underlying their heterogeneity and to identify whether such characteristics represent risk factors for patients with this disease, we performed an integrated genomic analysis of a large series of primary tumors. Identified are six molecular subgroups of medulloblastoma, each with a unique combination of numerical and structural chromosomal aberrations that globally influence mRNA and miRNA expression. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platforms:
GPL3720 GPL6801
121 Samples
Download data: CEL, TXT
Series
Accession:
GSE207762
ID:
200207762
6.

Integrative Genomic Analysis of Medulloblastoma Identifies a Molecular Subgroup That Drives Poor Clinical Outcome

(Submitter supplied) Medulloblastomas are heterogeneous tumors that collectively represent the most common malignant brain tumor in children. To understand the molecular characteristics underlying their heterogeneity and to identify whether such characteristics represent risk factors for patients with this disease, we performed an integrated genomic analysis of a large series of primary tumors. Identified are six molecular subgroups of medulloblastoma, each with a unique combination of numerical and structural chromosomal aberrations that globally influence mRNA and miRNA expression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL3921
214 Samples
Download data: CEL, GCT, XLS, XLSX
Series
Accession:
GSE202043
ID:
200202043
7.

MiR-1253 exerts tumor-suppressive effects in medulloblastoma via inhibition of CDK6 and CD276 (B7-H3)

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Methylation profiling by genome tiling array
Platforms:
GPL21145 GPL21697
216 Samples
Download data: IDAT
Series
Accession:
GSE148390
ID:
200148390
8.

MiR-1253 exerts tumor-suppressive effects in medulloblastoma via inhibition of CDK6 and CD276 (B7-H3) (RNA-seq dataset)

(Submitter supplied) Of the four primary subgroups of medulloblastoma, the most frequent cytogenetic abnormality, i17q, distinguishes Groups 3 and 4 which carry the highest mortality; haploinsufficiency of 17p13.3 is a marker for particularly poor prognosis. At the terminal end of this locus lies miR-1253, a brain-enriched microRNA that regulates bone morphogenic proteins during cerebellar development. We hypothesized miR-1253 confers novel tumor-suppressive properties in medulloblastoma. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21697
160 Samples
Download data: CSV
9.

MiR-1253 exerts tumor-suppressive effects in medulloblastoma via inhibition of CDK6 and CD276 (B7-H3) (Infinium MethylationEPIC dataset)

(Submitter supplied) Of the four primary subgroups of medulloblastoma, the most frequent cytogenetic abnormality, i17q, distinguishes Groups 3 and 4 which carry the highest mortality; haploinsufficiency of 17p13.3 is a marker for particularly poor prognosis. At the terminal end of this locus lies miR-1253, a brain-enriched microR that regulates bone morphogenic proteins during cerebellar development. We hypothesized miR-1253 confers novel tumor-suppressive properties in medulloblastoma. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL21145
56 Samples
Download data: IDAT, TXT
Series
Accession:
GSE148388
ID:
200148388
10.

mRNA expression data of 62 human medulloblastoma tumors

(Submitter supplied) To identify molecular subtypes of medulloblastoma we have profiled a series of 62 medulloblastoma tumors. Unsupervised hierarchical cluster analysis of these data identified 5 distinct molecular subtypes. Manuscript submitted. Title: Identification of medulloblastoma subtypes with distinct genetic profiles, pathway signatures and clinicopathological features. Authors: Marcel Kool, Jan Koster, Jens Bunt, Nancy E. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
62 Samples
Download data: CEL, CHP
Series
Accession:
GSE10327
ID:
200010327
11.

Human medulloblastoma samples

(Submitter supplied) Purpose Integrated genomics approaches have identified at least four distinct biological variants in medulloblastoma: WNT, SHH, group C, and group D. Non-WNT/Non-SHH tumors are associated with metastatic dissemination and an unfavorable prognosis. Additional markers may enhance outcome prediction in Non-WNT/Non-SHH medulloblastomas. Experimental Design We combined transcriptomic and DNA copy-number analyses for 64 primary medulloblastomas. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
64 Samples
Download data: TXT
Series
Accession:
GSE28245
ID:
200028245
12.

Molecular subgroups of adult medulloblastoma: a long-term single-institution study

(Submitter supplied) Background. Recent transcriptomic approaches have demonstrated that there are at least 4 distinct subgroups in medulloblastoma (MB); however, survival studies of molecular subgroups in adult MB have been inconclusive because of small sample sizes. The aim of this study is to investigate the molecular subgroups in adult MB and identify their clinical and prognostic implications in a large, single-institution cohort. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
13 Samples
Download data: TXT
Series
Accession:
GSE116028
ID:
200116028
13.

Microarray-based DNA methylation profiling of medulloblastoma and normal cerebellum samples

(Submitter supplied) Robust molecular subgrouping and copy-number profiling of medulloblastoma from small amounts of archival tumor material. Validation of patterns identified by whole-genome bisulphite sequencing in a larger cohort.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
284 Samples
Download data: TXT
Series
Accession:
GSE54880
ID:
200054880
14.

Genomics of medulloblastoma identifies four distinct molecular variants

(Submitter supplied) Recent genomic approaches have suggested the existence of multiple distinct subtypes of medulloblastoma. We studied a large cohort of medulloblastomas to determine how many subgroups of the disease exist, how they differ, and the extent of overlap between subgroups. We determined gene expression profiles and DNA copy number aberrations for 103 primary medulloblastomas. Bioinformatic tools were used for class discovery of medulloblastoma subgroups based on the most informative genes in the dataset. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5175
103 Samples
Download data: CEL
Series
Accession:
GSE21140
ID:
200021140
15.

Integrated analysis of genome-wide copy number and matched expression data reveals novel genes in esophageal adenocarcinoma

(Submitter supplied) The incidence of esophageal and junctional adenocarcinoma has increased 6-fold in the west in the last 30 years and 5 year survival remains <14%. We aimed to characterize genome-wide aberrations in esophageal adenocarcinoma to further understand disease pathogenesis and ultimately identify groups with differential survivals with implications for clinical management. Oligo-array-based high-resolution analysis of copy number changes in 89 fresh frozen esophageal adenocarcinoma resection sections with long-term clinical follow-up data was performed. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platform:
GPL8856
9 Samples
Download data: TXT
Series
Accession:
GSE25201
ID:
200025201
16.

Array CGH characterization of esophago-gastric adenocarcinoma

(Submitter supplied) The incidence of esophageal and junctional adenocarcinoma has increased 6-fold in the west in the last 30 years and 5 year survival remains <14%. We aimed to characterize genome-wide aberrations in esophageal adenocarcinoma to further understand disease pathogenesis and ultimately identify groups with differential survivals with implications for clinical management. Oligo-array-based high-resolution analysis of copy number changes in 89 fresh frozen esophageal adenocarcinoma resection sections with long-term clinical follow-up data was performed. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL10001
56 Samples
Download data: GPR
Series
Accession:
GSE20154
ID:
200020154
17.

Integrated array-CGH and expression microarray analyses on medulloblastomas in heterozygous Ptch1 mice

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Genome variation profiling by genome tiling array
Platforms:
GPL7202 GPL9727 GPL9729
30 Samples
Download data: TXT
Series
Accession:
GSE19384
ID:
200019384
18.

Integrated array-CGH and expression microarray analyses on medulloblastomas in heterozygous Ptch1 mice, aCGH 2

(Submitter supplied) Genomic radiation signature illuminates low-dose effects with sharply reflected transcriptome in Ptch1-deficient medulloblastomas. Cancer risks of low-dose radiation are of great concern especially in relation to rapidly increasing medical exposures; however, their accurate assessments cope with many challenges and difficulties, partly due to the inability to distinguish radiation-induced tumors from spontaneous ones. more...
Organism:
Mus musculus
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9729
3 Samples
Download data: TXT
Series
Accession:
GSE19382
ID:
200019382
19.

Integrated array-CGH and expression microarray analyses on medulloblastomas in heterozygous Ptch1 mice, aCGH 1

(Submitter supplied) Genomic radiation signature illuminates low-dose effects with sharply reflected transcriptome in Ptch1-deficient medulloblastomas. Cancer risks of low-dose radiation are of great concern especially in relation to rapidly increasing medical exposures; however, their accurate assessments cope with many challenges and difficulties, partly due to the inability to distinguish radiation-induced tumors from spontaneous ones. more...
Organism:
Mus musculus
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9727
12 Samples
Download data: TXT
Series
Accession:
GSE19381
ID:
200019381
20.

Integrated array-CGH and expression microarray analyses on medulloblastomas in heterozygous Ptch1 mice, expression

(Submitter supplied) Genomic radiation signature illuminates low-dose effects with sharply reflected transcriptome in Ptch1-deficient medulloblastomas. Cancer risks of low-dose radiation are of great concern especially in relation to rapidly increasing medical exposures; however, their accurate assessments cope with many challenges and difficulties, partly due to the inability to distinguish radiation-induced tumors from spontaneous ones. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
15 Samples
Download data: TXT
Series
Accession:
GSE19360
ID:
200019360
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