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Links from GEO DataSets

Items: 20

1.

Array CGH data of 64 prostate cancer specimens

(Submitter supplied) The dataset comprises array CGH data of 64 prostate cancer specimens performed on Stanford cDNA microarrays, to accompany the study of J Lapointe et al (2007). For each array, Channel 2 represents Cy5-labeled prostate genomic DNA, and Channel 1 Cy3-labeled normal male genomic DNA. Set of arrays organized by shared biological context, such as organism, tumors types, processes, etc. Keywords: Logical Set, array CGH
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platforms:
GPL4640 GPL4639
64 Samples
Download data
Series
Accession:
GSE6469
ID:
200006469
2.

Integrative Analysis of Genomic Aberrations Associated with Prostate Cancer Progression

(Submitter supplied) Genome-wide copy number changes were monitored using array comparative genomic hybridization (aCGH) of laser-capture microdissected prostate cancer samples spanning stages of prostate cancer progression including precursor lesions, clinically localized disease and metastatic disease. A total of 62 specific cell populations from 38 patients were profiled. Keywords: Disease state analysis using array-based comparatavie genomic hybridization
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL2013
64 Samples
Download data: GPR
Series
Accession:
GSE8026
ID:
200008026
3.

Genome-wide screening for complete genetic loss in PCa by CGH onto cDNA arrays

(Submitter supplied) We demonstrate that comparative genomic hybridisation (CGH) onto cDNA microarrays may be used to carry out genome-wide screens for regions of genetic loss, including homozygous (complete) deletions that may represent the possible location of tumour suppressor genes in human cancer. Screening of the prostate cancer cell lines LNCaP, PC3 and DU145 allowed the mapping of specific regions where genome copy number appeared altered and led to the identification of two novel regions of complete loss at 17q21.31 (500 kb spanning STAT3) and at 10q23.1 (50-350 kb spanning SFTPA2) in the PC3 cell line. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL3898
8 Samples
Download data
Series
Accession:
GSE6138
ID:
200006138
4.

CGH profiling of 26 Ewing Sarcoma tumour samples

(Submitter supplied) Ewing’s Sarcoma (ES) is characterized by specific chromosomal translocations, the most common being t(11;22)(q24;q12). Additionally, other types of genetic abnormalities may occur and be relevant to explain the variable tumoural biology and clinical outcome. We have carried out a high-resolution array CGH and expression profiling on 25 ES tumour samples to characterize the DNA copy number aberrations (CNA) occurring in these tumours and to determine their association with gene expression profiles (GEO Series accession number: GSE8303) and their clinical outcome. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL2879
25 Samples
Download data: TXT
Series
Accession:
GSE8398
ID:
200008398
5.

Gene expression profiling and array CGH in Ewing's sarcoma

(Submitter supplied) According to array-CGH data tumors were segregated in two different groups: one genomic stable and other genomic unstable. The genomic unstable group showed a statistically significant shorter overall survival ans was more refractory to chemotherapy. Gene expression profile revealed that genes related with chromosome segregation, DNA repair pathways and cell cycle control were upregulated in the genomic unstable group Keywords: Tumor comparison
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL2891
14 Samples
Download data: TXT
Series
Accession:
GSE8303
ID:
200008303
6.

CGH profiling of 87 indolent non-hodgkin’s lymphoma (NHL)

(Submitter supplied) BACKGROUND AND OBJECTIVES: Low-grade B-cell lymphomas include several subtypes of tumors with different degrees of histological, biological or clinical features. Differential diagnosis is frequently compromised by the lack of specific cytogenetic or molecular features. As a consequence, therapies remain in many lymphoma types largely based in common protocols with largely variable success. Our objectives were to describe and to compare the genomic profile of a series of samples from the most prevalent low-grade lymphoma subtypes; all of them systematically analyzed with the same approach. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL2879
87 Samples
Download data: TXT
Series
Accession:
GSE8918
ID:
200008918
7.

Gene profiling of primary cultures from human prostate tumors

(Submitter supplied) The histopathological and molecular heterogeneity of prostate cancer and the limited availability of human tumor tissue make unraveling the mechanisms of prostate carcinogenesis a challenging task. Our goal was to develop an ex vivo model that could be reliably utilized to define a prognostic signature based on gene expression profiling of cell cultures that maintained the tumor phenotype. To this end, we derived epithelial cultures from tissue explanted from 59 patients undergoing radical prostatectomy or cistoprostatectomy because of Prostate Benign Hyperplasia/Prostate Cancer or Bladder Carcinoma. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1746
Platform:
GPL96
30 Samples
Download data
Series
Accession:
GSE3868
ID:
200003868
8.
Full record GDS1746

Primary epithelial cell cultures from prostate tumors

Analysis of epithelial cell cultures from prostate tumor explants. Results identify an epithelial-restricted transcription profile that can be integrated with tumor grade and clinical information with the aim of discriminating indolent and aggressive prostate tumors that are histologically similar.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 7 disease state, 2 protocol sets
Platform:
GPL96
Series:
GSE3868
30 Samples
Download data
DataSet
Accession:
GDS1746
ID:
1746
9.

Chromosomal aberrations in benign and malignant salivary gland myoepitheliomas

(Submitter supplied) Salivary gland myoepithelial tumors are relatively uncommon tumors with an unpredictable clinical course. More knowledge about their genetic profiles is necessary to identify novel predictors of disease. In this study, we subjected 27 primary tumors (15 myoepitheliomas and 12 myoepithelial carcinomas) to genome-wide microarray-based comparative genomic hybridization (array CGH). We set out to delineate known chromosomal aberrations in more detail and to unravel chromosomal differences between benign myoepitheliomas and myoepithelial carcinomas. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platforms:
GPL7394 GPL5477 GPL2843
28 Samples
Download data
Series
Accession:
GSE12951
ID:
200012951
10.

Genomic copy number alterations as predictive markers in breast cancer

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL5772
118 Samples
Download data: GPR
Series
Accession:
GSE10181
ID:
200010181
11.

Genomic copy number alterations as predictive markers of neoadjuvant chemotherapy response in breast cancer

(Submitter supplied) Array CGH containing 4,044 human bacterial artificial chromosome clones was used to assess different copy number changes between chemotherapy responsive and non-resposive breast cancer tissues. Keywords: Array CGH
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL5772
56 Samples
Download data: GPR
Series
Accession:
GSE10129
ID:
200010129
12.

Genomic copy number alterations as predictive markers of systemic recurrence in breast cancer

(Submitter supplied) Array CGH containing 4,044 human bacterial artificial chromosome clones was used to assess copy number changes in 31 pairs of clinicopathologically well matched recurred / nonrecurred breast cancer tissues. Keywords: array CGH
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL5772
62 Samples
Download data: GPR
Series
Accession:
GSE10128
ID:
200010128
13.

Integrative Genome-wide Analysis of Glioblastoma.

(Submitter supplied) Glioblastoma multiforme shows multiple chromosomal aberrations, the impact of which on gene expression remains unclear. To investigate this relationship and to identify putative initiating genomic events, we integrated a paired copy number and gene expression survey in glioblastoma using whole human genome arrays. Loci of recurrent copy number alterations were combined with gene expression profiles obtained on the same tumor samples. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array; Expression profiling by genome tiling array
Platforms:
GPL6480 GPL2879
60 Samples
Download data: TXT
Series
Accession:
GSE10878
ID:
200010878
14.

Expression profile of ovarian tumour samples

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
295 Samples
Download data: CEL, CSV
Series
Accession:
GSE9899
ID:
200009899
15.

Expression profile of 285 ovarian tumour samples

(Submitter supplied) We used microarrays to profile the expression levels of 285 ovarian samples in order to identify molecular subtypes of the tumour Keywords: disease state analysis
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
285 Samples
Download data: CEL, CSV
Series
Accession:
GSE9891
ID:
200009891
16.

Expression profile of 5 ovarian tumour samples (two different cell types from each sample profiles)

(Submitter supplied) We used microarrays to profile the expression levels of 5 tumour samples Keywords: expression difference of cell types in tumour samples
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
10 Samples
Download data: CEL, CSV
Series
Accession:
GSE9890
ID:
200009890
17.

Gene expression profile of Transgenic Adenocarcinoma of the Mouse Prostate (TRAMP)

(Submitter supplied) Gene expression profile of Transgenic Adenocarcinoma of the Mouse Prostate (TRAMP) reveals murine targets for preclinical development of human prostate cancer therapy In this study, we have generated an open source TRAMP microarray dataset to identify differentially expressed genes from human prostate cancer that have concordant expression in TRAMP tumors, and thereby represent lead targets for preclinical therapy development. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
18 Samples
Download data: CEL
Series
Accession:
GSE10525
ID:
200010525
18.

Gene expression profiling of prostate cancer

(Submitter supplied) To better understand the molecular mechanism that underlay tumorigenesis and progression of prostate cancer (PCa), we studied the gene expression profiles of sixteen PCa compared to their matched normal tissues. Using Significance Analysis of Microarrays, we identified 53 genes differentially expressed that were more than 2 fold up- or down-regulated in at least 50 % of the tumors. Keywords: disease state analysis
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1998
16 Samples
Download data: GPR
Series
Accession:
GSE9347
ID:
200009347
19.

Comparative analyses of chromosome alterations in metastases in castration-resistant prostate cancer patients

(Submitter supplied) Androgen deprivation is the mainstay of therapy for progressive prostate cancer. Despite initial and dramatic tumor inhibition, most men eventually fail therapy and die of metastatic castration-resistant (CR) disease. Here, we characterize the profound degree of genomic alteration found in CR tumors using array CGH, gene expression arrays, and FISH. By cluster analysis, we show that the similarity of the genomic profiles from primary and metastatic tumors is driven by the patient. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL6737
54 Samples
Download data: GPR
Series
Accession:
GSE18259
ID:
200018259
20.

High-resolution genome-wide copy-number analysis suggests a monoclonal origin of multi-focal prostate cancer

(Submitter supplied) Many human cancers present as multi-focal lesions. Understanding the clonal origin of multi-focal cancers is of both etiological and clinical importance. The molecular basis of multi-focal prostate cancer has previously been explored using only a limited number of isolated markers and, although independent origin is widely believed, the clonal origin of multi-focal prostate cancer is still debatable. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array; SNP genotyping by SNP array
Platform:
GPL6801
66 Samples
Download data: CEL, CHP
Series
Accession:
GSE29569
ID:
200029569
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