U.S. flag

An official website of the United States government

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO DataSets

Items: 20

1.

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:
GPL2879 GPL6480
60 Samples
Download data: TXT
Series
Accession:
GSE10878
ID:
200010878
2.

Combined arrayCGH and SNP-loss of heterozygosity analysis in cervical cancer

(Submitter supplied) BACKGROUND: Cervical carcinoma develops as a result of multiple genetic alterations. Different studies investigated genomic alterations in cervical cancer mainly by means of metaphase comparative genomic hybridization (mCGH) and microsatellite marker analysis for the detection of loss of heterozygosity (LOH). Currently, high throughput methods such as array comparative genomic hybridization (array CGH), single nucleotide polymorphism array (SNP array) and gene expression arrays are available to study genome-wide alterations. more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by genome tiling array; Genome variation profiling by SNP array; SNP genotyping by SNP array
Platforms:
GPL2641 GPL4012 GPL201
40 Samples
Download data: CEL, GPR
Series
Accession:
GSE8605
ID:
200008605
3.

Classification of neuroblastoma by integrating gene expression pattern with regional alterations in DNA copy number

(Submitter supplied) The specific genes that influence neuroblastoma biology and are targeted by genomic alterations remain largely unknown. We quantified mRNA expression in a highly annotated series of 101 prospectively collected diagnostic neuroblastoma primary tumors and the expression profiles were determined using Affymetrix U95Av2 arrays. Comparisons between the sample groups allow the identification of genes with localized expression patterns. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL8300
102 Samples
Download data: CEL
Series
Accession:
GSE3960
ID:
200003960
4.

A SNP microarray and FISH-based procedure to detect allelic imbalances in multiple myeloma

(Submitter supplied) A SNP microarray and FISH-based procedure to detect allelic imbalances in multiple myeloma: an integrated genomics approach reveals a wide dosage effect on gene and microRNA expression This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by SNP array
Platforms:
GPL96 GPL2005
203 Samples
Download data: CEL
Series
Accession:
GSE16122
ID:
200016122
5.

Integrated genomics approach to detect allelic imbalances in multiple myeloma, SNP data

(Submitter supplied) A SNP microarray and FISH-based procedure to detect allelic imbalances in multiple myeloma: an integrated genomics approach reveals a wide dosage effect on gene and microRNA expression Multiple myeloma (MM) is characterized by marked genomic instability. Beyond structural rearrangements, a relevant role in its biology is represented by allelic imbalances leading to significant variations in ploidy status. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platform:
GPL2005
45 Samples
Download data: CEL
Series
Accession:
GSE16121
ID:
200016121
6.

Integrated genomics approach to detect allelic imbalances in multiple myeloma

(Submitter supplied) Multiple myeloma (MM) is characterized by marked genomic instability. Beyond structural rearrangements, a relevant role in its biology is represented by allelic imbalances leading to significant variations in ploidy status. To better elucidate the genomic complexity of MM, we analyzed a panel of 45 patients using combined FISH and microarray approaches. Using a self-developed procedure to infer exact local copy numbers for each sample, we identified a significant fraction of patients showing marked aneuploidy. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
158 Samples
Download data: CEL
Series
Accession:
GSE13591
ID:
200013591
7.

Non Small Cell Lung Cancer

(Submitter supplied) This series contain 36 samples obtained from human lung tissue and includes the following: 7 Adenocarcinoma samples. 16 Squamous cell carcinoma samples. 1 AdenoSquamous sample. 2 Renal Metastasis. 1 Colon metastasis. 7 normal lung tissue adjacent to the tumors. 2 commercial normal lung RNA. Keywords = Lung Keywords = Non Small Cell Lung Cancer Keywords = Adenocarcinoma Keywords = Squamous Cell Carcinoma Keywords = Normal Lung. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL91
37 Samples
Download data
Series
Accession:
GSE1987
ID:
200001987
8.

Genome-wide characterization of gene expression variations and DNA copy number changes in prostate cancer cell lines

(Submitter supplied) Abstract: BACKGROUND: The aim of this study was to characterize gene expression and DNA copy number profiles in androgen sensitive (AS) and androgen insensitive (AI) prostate cancer cell lines on a genome-wide scale. METHODS: Gene expression profiles and DNA copy number changes were examined using DNA microarrays in eight commonly used prostate cancer cell lines. Chromosomal regions with DNA copy number changes were identified using cluster along chromosome (CLAC). more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by array
Platforms:
GPL3355 GPL3341
16 Samples
Download data
Series
Accession:
GSE4396
ID:
200004396
9.

DNA copy number changes in prostate cancer cell lines

(Submitter supplied) Abstract: BACKGROUND: The aim of this study was to characterize gene expression and DNA copy number profiles in androgen sensitive (AS) and androgen insensitive (AI) prostate cancer cell lines on a genome-wide scale. METHODS: Gene expression profiles and DNA copy number changes were examined using DNA microarrays in eight commonly used prostate cancer cell lines. Chromosomal regions with DNA copy number changes were identified using cluster along chromosome (CLAC). more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL3355
8 Samples
Download data
Series
Accession:
GSE4017
ID:
200004017
10.

Gene expression variations in prostate cancer cell lines

(Submitter supplied) Abstract: BACKGROUND: The aim of this study was to characterize gene expression and DNA copy number profiles in androgen sensitive (AS) and androgen insensitive (AI) prostate cancer cell lines on a genome-wide scale. METHODS: Gene expression profiles and DNA copy number changes were examined using DNA microarrays in eight commonly used prostate cancer cell lines. Chromosomal regions with DNA copy number changes were identified using cluster along chromosome (CLAC). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1699
Platform:
GPL3341
8 Samples
Download data
Series
Accession:
GSE4016
ID:
200004016
11.
Full record GDS1699

Androgen sensitive and insensitive prostate cancer cell lines: expression profiles

Analysis of androgen sensitive (AS) and insensitive (AI) prostate cancer cell lines. Despite the wide use of these cell lines as model systems, a global genotypic characterization of these cell lines is currently lacking. Results identify differences in gene expression profiles.
Organism:
Homo sapiens
Type:
Expression profiling by array, log2 ratio, 8 cell line, 2 cell type sets
Platform:
GPL3341
Series:
GSE4016
8 Samples
Download data
DataSet
Accession:
GDS1699
ID:
1699
12.

Array CGH reveals genetic homogeneity and frequent copy number increases encompassing CCNE1 in Fallopian tube carcinoma

(Submitter supplied) Fallopian tube carcinoma (FTC) is a rare, poorly studied and aggressive cancer, associated with poor survival. Since tumorigenesis is related to acquisition of genetic changes, we used genome-wide array CGH to analyze copy number aberrations occurring in FTC in order to obtain a better understanding of FTC carcinogenesis and to identify prognostic events and targets for therapy. We used arrays of 2464 genomic clones, providing ~1.4 Mb resolution across the genome to quantitatively map genomic DNA copy number aberrations from fourteen FTC onto the human genome sequence. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL4896
14 Samples
Download data: TXT
Series
Accession:
GSE7180
ID:
200007180
13.

SCLC cell line profiling on HG-U133A arrays

(Submitter supplied) RNA expression analysis was performed to compare patterns to DNA copy number changes and sensitivity to BCL2 inhibitors. Keywords: cell line comparison
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3029
Platform:
GPL571
34 Samples
Download data: CEL
Series
Accession:
GSE7097
ID:
200007097
14.
Full record GDS3029

Small-cell lung carcinoma cell lines of varying sensitivity to a Bcl-2 antagonist

Analysis of small-cell lung carcinoma cell (SCLC) lines. Expression profiles compared to the cell lines' sensitivity to the Bcl-2 antagonist ABT-737 and chromosomal gains that include changes in Bcl-2 gene copy number. ABT-737 induces the regression of a fraction of SCLC solid tumors.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 cell type, 4 genotype/variation sets
Platform:
GPL571
Series:
GSE7097
34 Samples
Download data: CEL
DataSet
Accession:
GDS3029
ID:
3029
15.

Array-CGH in human glial brain tumors

(Submitter supplied) Set of arrays organized by shared biological context, such as organism, tumors types, processes, etc. Characterization of DNA copy number changes in 54 glial brain tumors using a cDNA microarray-based comparative genomic hybridization method. Tumors: 54 fresh-frozen glioma specimens subjected to standard WHO classification. Specimens included astrocytic [3 juvenile pilocytic astrocytomas, 1 low-grade astrocytic glioma, 3 anaplastic astrocytomas, 31 glioblastomas (of these 3 secondary glioblastomas and 2 gliosarcomas)], oligodendroglial [5 oligodendrogliomas, 3 anaplastic oligodendrogliomas], and 7 anaplastic oligoastrocytomas tumors. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL1715
54 Samples
Download data
Series
Accession:
GSE1991
ID:
200001991
16.

Multi-dimensional genomic analysis in breast cancer patients

(Submitter supplied) Multi-dimensional genomic analysis identifies a class of breast cancer patients with high metastatic outcome and differential response to chemotherapeutic drugs The application of multi-dimensional genomic analyses might provide a more refined risk assessment of breast tumor aggressiveness and improve the selection of patients for personalized medicine. Our study demonstrates the feasibility of using CNAs to predict patient outcome. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platforms:
GPL2004 GPL2005
626 Samples
Download data: CEL
Series
Accession:
GSE10099
ID:
200010099
17.

High resolution array-CGH and expression profiling identifies a novel genomic subtype of ER negative breast cancer

(Submitter supplied) An oligo array based high-resolution analysis of copy number alterations in 171 primary breast tumors of relatively small size and low NPI, and 49 breast cancer cell-lines. Objectives of the study were to study the molecular taxonomy and the genomic aberration patterns in a breast cancer cohort representative of breast cancer demographics. Keywords: array comparative genomic hybridisation
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL5737
220 Samples
Download data: TXT
Series
Accession:
GSE8757
ID:
200008757
18.

Human myeloma cell lines gene expression profiling

(Submitter supplied) In order to investigate the patterns of genetic lesions in a panel of 23 Human Multiple Myeloma Cell Lines (HMCLs), we made a genomic integrative analysis involving FISH and both gene expression and genome-wide profiling approaches. The expression profiles of the genes targeted by the main IGH translocations showed that the WHSC1/MMSET gene involved in t(4;14)(p16;q32) was expressed at different levels in all of the HMCLs, and that the expression of the MAF gene was not restricted to the HMCLs carrying t(14;16)(q32;q23). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
23 Samples
Download data: CEL
Series
Accession:
GSE6205
ID:
200006205
19.

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
20.

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:
GPL2843 GPL5477 GPL7394
28 Samples
Download data
Series
Accession:
GSE12951
ID:
200012951
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=1|qty=2|blobid=MCID_6748d37f43705129cf49f471|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
   Taxonomic Groups  [List]
Tree placeholder
    Top Organisms  [Tree]

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center