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.

caArray_notte-00422: Molecular Dissection of Colon Cancer

(Submitter supplied) RNA expression data was generated as part of a colon cancer study. Samples were obtained from patients, including primary colon cancer, polyps, metastases, and matched normal mucosa (obtained from the margins of the resection). The RNA was extracted from tissue samples obtained from resections and hybridized to Affymetrix HG-U133 arrays. RNA expression data was also obtained for a few cell lines.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
390 Samples
Download data: CEL, CHP
Series
Accession:
GSE68468
ID:
200068468
2.

Expression data from colorectal cancer patients

(Submitter supplied) The study consist of patients who presented at Memorial Sloan-Kettering Cancer Center with a colonic neoplasm between 1992 and 2004. Biological specimens used in this study include primary colon adenocarcinomas, adenomas, metastasis and corresponding normal mucosae.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
390 Samples
Download data: CEL, TXT
Series
Accession:
GSE41258
ID:
200041258
3.

Multiple genes at the chromosome 20q amplicon contribute to colorectal adenoma to carcinoma progression

(Submitter supplied) Chromosomal instability (CIN) is the hallmark of colorectal adenoma to carcinoma progression in 85% of cases, with 20q gain as the most prominent aberration. Yet, the oncogenes at this chromosomal gain are still largely unknown. Here, we aimed to identify oncogenes at 20q involved in colorectal adenoma to carcinoma progression by measuring the effect of 20q gain on gene expression in this amplicon. more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by genome tiling array
5 related Platforms
217 Samples
Download data
Series
Accession:
GSE8067
ID:
200008067
4.

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
5.

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
6.

Candidate driver genes in focal chromosomal aberrations of stage II colon cancer

(Submitter supplied) Chromosomal instable colorectal cancer is marked by specific large chromosomal copy number aberrations. Recently, focal aberrations of 3Mb or smaller have been identified as a common phenomenon in cancer. Inherent to their limited size, these aberrations harbour one or few genes. The aim of this study is to identify recurrent focal chromosomal aberrations and their candidate driver genes in a well defined series of stage II colon cancers and assess their potential clinical relevance. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array; Expression profiling by array
4 related Platforms
61 Samples
Download data: PAIR, TXT
Series
Accession:
GSE17047
ID:
200017047
7.

Genomic Profiles Associated with Early Micrometastasis in Lung Cancer: Relevance of 4q Deletion

(Submitter supplied) PURPOSE: Bone marrow (BM) is a common homing organ for early disseminated tumor cells (DTC) and their presence can predict the subsequent occurrence of overt metastasis and survival in lung cancer. It is still unclear whether the shedding of DTC from the primary tumor is a random process or a selective release driven by a specific genomic pattern. EXPERIMENTAL DESIGN: DTCs were identified in BM from lung cancer patients by an immunocytochemical cytokeratin assay. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platforms:
GPL3055 GPL2819
30 Samples
Download data
Series
Accession:
GSE13191
ID:
200013191
8.

Gene expression profile of lung tumors

(Submitter supplied) We have investigated whether the early dissemination of tumor cells into bone marrow is associated with a specific molecular pattern in primary lung cancer Keywords: primary lung tumor tissue and normal bronchial epithelial tissue
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
19 Samples
Download data: CEL
Series
Accession:
GSE10799
ID:
200010799
9.

A Genome-wide Study of Cytogenetic Changes in Colorectal Cancer Using SNP Microarrays: Possibilities for Future Personalized Treatment

(Submitter supplied) In colorectal cancer (CRC), chromosomal instability (CIN) is typically studied using comparative-genomic hybridization (CGH) arrays. We studied paired (tumor and surrounding healthy) fresh-frozen tissue from 86 CRC patients using Illumina’s Infinium-based SNP array. This method allowed us to study CIN in CRC, with simultaneous analysis of copy number (CN) and B-allele frequency (BAF), which is a representation of allelic composition. more...
Organism:
Homo sapiens
Type:
SNP genotyping by SNP array; Genome variation profiling by SNP array
Platforms:
GPL8887 GPL13829
172 Samples
Download data: TXT
Series
Accession:
GSE34678
ID:
200034678
10.

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
11.
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
12.

SNP array analysis of chromosomal instability patterns discriminates rectal adenomas from carcinomas

(Submitter supplied) Total mesorectal excision (TME) is the standard treatment for rectal cancer, while transanal endoscopic microsurgery (TEM) is a recently introduced surgical approach for the treatment of rectal adenomas. Incorrect preoperative staging before TEM is a problem. To identify genetic changes that might correlate with tumour stage and could lead to optimized treatment selection we performed a genome-wide chromosomal instability search in a homogeneous, clinical cohort of rectal tumours. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array; SNP genotyping by SNP array
Platforms:
GPL1266 GPL2641
97 Samples
Download data: CEL, CHP
Series
Accession:
GSE7946
ID:
200007946
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.

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
15.

Integrating chromosomal aberrations and gene expression profiles to dissect rectal cancer

(Submitter supplied) Accurate staging of rectal tumors is essential for making the correct treatment choice. In a previous study, we found that loss of 17p, 18q and gain of 8q, 13q and 20q could distinguish adenoma from carcinoma tissue and that loss of 1q was related to lymph node metastasis. In order to find markers for tumor staging, we searched for candidate genes on these specific chromosomes. We performed gene expression microarray analysis on 79 rectal tumors and integrated these data with genomic data from the same sample series (Series GSE7946, Samples GSM194994-GSM195028). more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by SNP array; SNP genotyping by SNP array
Platforms:
GPL3676 GPL2641
114 Samples
Download data: CEL, CHP, GPR
Series
Accession:
GSE12225
ID:
200012225
16.

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 GPL2843 GPL5477
28 Samples
Download data
Series
Accession:
GSE12951
ID:
200012951
17.

SNP expression data from breast cancer

(Submitter supplied) SNP Expression profiling of human breast cancer: 29 tumor samples, 4 pure normal breat samples and 8 lymphocytes samples Keywords: Human Cancer
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platform:
GPL2005
41 Samples
Download data
Series
Accession:
GSE5927
ID:
200005927
18.

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
19.

caArray_jacks-00113: Murine KRASLA lung cancer gene expression

(Submitter supplied) Tumors from 5-6 month old KrasLA mice were dissected. Gene expression analysis on U74A affy chips. 19 normal lungs from age matched controls were also includeed **NOTE: Migrated from caArray 1.x, identifier='gov.nih.nci.ncicb.caarray:Experiment:1015897590231167:1'
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL81
58 Samples
Download data: CEL
Series
Accession:
GSE70271
ID:
200070271
20.

DNA copy number changes in colorectal flat adenomas

(Submitter supplied) Background & aim: Flat adenomas form a specific phenotype of colorectal adenomas that has been associated with more severe molecular changes and consequently a more aggressive clinical behavior compared to their polypoid counterparts. In the present study we set out to compare one of the molecular changes most explicitly associated with adenoma to carcinoma progression, i.e. chromosomal instability, between flat and polypoid colorectal adenomas. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL8687
118 Samples
Download data
Series
Accession:
GSE30479
ID:
200030479
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=1|qty=3|blobid=MCID_674c5437d82608403851f7fd|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