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Links from GEO DataSets

Items: 20

1.

Gastric cancer tumor tissue samples and cell lines vs normal sample

(Submitter supplied) We analyzed DNA copy number alterations in 64 human gastric cancer samples and 8 gastric cancer cell lines using bacterial artificial chromosome (BAC) arrays based comparative genomic hybridisation (aCGH).
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL14846
72 Samples
Download data: TXT
Series
Accession:
GSE33501
ID:
200033501
2.

Cancer Samples vs. Matched Adjacent Noncancerous Samples

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by genome tiling array
Platforms:
GPL5175 GPL9128
77 Samples
Download data: CEL, TXT
Series
Accession:
GSE33429
ID:
200033429
3.

Copy number variation profiling of gastric tissues: Cancer Samples vs. Matched Adjacent Noncancerous Samples

(Submitter supplied) Copy number variation profiling of gastric tissues comparing gastric cancer tissues with matched adjacent noncancerous tissues. Goal was to determine the effects of chromosomal imbalances on gene expression and carcinogenesis or progression.
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9128
27 Samples
Download data: TXT
Series
Accession:
GSE33428
ID:
200033428
4.

Expression data from gastric tissues: Cancer Samples vs. Matched Adjacent Noncancerous Samples

(Submitter supplied) To elucidate gene expression associated with copy number changes, we performed a genome-wide copy number and expression microarray analysis of 25 pairs of gastric tissues.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5175
50 Samples
Download data: CEL
Series
Accession:
GSE33335
ID:
200033335
5.

Detection of novel amplification units in prostate cancer

(Submitter supplied) Genome-wide screening for regions of genetic gains and losses on nine prostate cancer cell lines (PC3, DU145, LNCaP, CWR22, and derived sublines) was carried out using comparative genomic hybridization on a 35 K longmer oligonucleotide microarray (arrayCGH). Compared to conventional chromosomal CGH more deletions and small regions of gains, particularly in pericentromeric regions and regions next to the telomers, were detected. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL5046
11 Samples
Download data: TXT
Series
Accession:
GSE7376
ID:
200007376
6.

Losses of chromosome 5q and 14q mark a subset of gastric cancers with good clinical outcome

(Submitter supplied) Purpose: To improve clinical outcome of gastric cancer patients, most emphasis is on improving therapeutic regimens, including more extensive surgery as well as (neo)adjuvant chemotherapy. The present study set out to identify, based on DNA copy number profiling, subgroups of patients with different clinical outcomes who thus would qualify for different therapy intensities. Experimental Design: DNA of 206 gastric cancer patients was isolated and analyzed by genome wide array comparative genomic hybridization. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
4 related Platforms
183 Samples
Download data: TXT
Series
Accession:
GSE26389
ID:
200026389
7.

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
8.

Global analysis of DNA methylation changes during progression of oral tumorigenesis

(Submitter supplied) Objectives: Earlier studies involving a priori gene selection have identified promoter regions deregulated by DNA methylation changes in oral squamous cell cancers (OSCCs) and precancers. Interrogation of global DNA methylation patterns for such specimens has not been reported, though such analyses are needed to uncover novel molecular factors driving disease. Materials and Methods: We evaluated global DNA methylation patterns for 30 biopsies obtained from 10 patients undergoing surgical removal of an OSCC or carcinoma in situ (CIS). more...
Organism:
Homo sapiens
Type:
Methylation profiling by array; Expression profiling by array
Platforms:
GPL6480 GPL8490
60 Samples
Download data: TXT
Series
Accession:
GSE46802
ID:
200046802
9.

Oral dysplasias and oral squamous cell carcinoma

(Submitter supplied) Analysis of DNA from 94 oral lesions by whole genome tiling-path array comparative genomic hybridization. Keywords: array comparative genomic hybridization
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platforms:
GPL2043 GPL2616
94 Samples
Download data: TXT
Series
Accession:
GSE9193
ID:
200009193
10.

Identification of Tumor Suppressors and Oncogenes from Genomic and Epigenetic Features in Ovarian Cancer

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Methylation profiling by genome tiling array; Genome variation profiling by genome tiling array
Platforms:
GPL8581 GPL96 GPL13248
139 Samples
Download data: CEL, FTR, GPR, TXT
Series
Accession:
GSE28015
ID:
200028015
11.

Representational Oligonucleotide Microarray Analysis (ROMA) array for Copy Number Variation Detection.

(Submitter supplied) The identification of genetic and epigenetic alterations from primary tumor cells has become a common method to identify genes critical to the development and progression of cancer. We provide a bioinformatic analysis of copy number variation and DNA methylation covering the genetic landscape of ovarian cancer tumor cells. We individually examined the copy number variation and DNA methylation for 44 primary ovarian cancer samples and 7 ovarian normal samples using our MOMA-ROMA technology and Affymetrix expression data as well as 379 tumor samples analyzed by The Cancer Genome Atlas. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL8581
42 Samples
Download data: GPR, TXT
Series
Accession:
GSE28013
ID:
200028013
12.

Gene Expression Array of Human Ovarian Cancer.

(Submitter supplied) The identification of genetic and epigenetic alterations from primary tumor cells has become a common method to identify genes critical to the development and progression of cancer. We provide a bioinformatic analysis of copy number variation and DNA methylation covering the genetic landscape of ovarian cancer tumor cells. We individually examined the copy number variation and DNA methylation for 44 primary ovarian cancer samples and 7 ovarian normal samples using our MOMA-ROMA technology and Affymetrix expression data as well as 379 tumor samples analyzed by The Cancer Genome Atlas. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
46 Samples
Download data: CEL
Series
Accession:
GSE27943
ID:
200027943
13.

Methylation detection Oligonucleotide Microarray Analysis: high resolution method for CpG island methylation detection 3.

(Submitter supplied) The identification of genetic and epigenetic alterations from primary tumor cells has become a common method to identify genes critical to the development and progression of cancer. We provide a bioinformatic analysis of copy number variation and DNA methylation covering the genetic landscape of ovarian cancer tumor cells. We individually examined the copy number variation and DNA methylation for 44 primary ovarian cancer samples and 7 ovarian normal samples using our MOMA-ROMA technology and Affymetrix expression data as well as 379 tumor samples analyzed by The Cancer Genome Atlas. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13248
51 Samples
Download data: FTR, TXT
Series
Accession:
GSE27940
ID:
200027940
14.

Integrative Genomics Reveals Mechanisms of Copy Number Alterations Responsible for Transcriptional Deregulation in Colorectal Cancer

(Submitter supplied) To evaluate the mechanisms and consequences of chromosomal aberrations in colorectal cancer (CRC), we used a combination of spectral karyotyping, array comparative genomic hybridization (aCGH), and array-based global gene expression profiling on 31 primary carcinomas and 15 established cell lines. Importantly, aCGH showed that the genomic profiles of primary tumors are recapitulated in the cell lines. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL6848 GPL6480
50 Samples
Download data: TXT
Series
Accession:
GSE126053
ID:
200126053
15.

cis-Expression QTL Analysis of Established Risk Variants for Colorectal Cancer

(Submitter supplied) Genome-wide association studies (GWAS) have identified 19 risk variants associated with colorectal cancer. As most of these risk variants reside outside the coding regions of genes, we conducted cis-expression quantitative trait loci (cis-eQTL) analyses to investigate possible regulatory functions on the expression of neighboring genes.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5175
80 Samples
Download data: CEL
Series
Accession:
GSE31737
ID:
200031737
16.

Identification of novel candidate oncogenes in chromosomal region 17p11.2-p12 in human osteosarcoma

(Submitter supplied) in 25% - 30% of all OS cases the chromosome region 17p11.2-p12 is aberrant. Using SNP array in conjunction with expression microarrays we try to identify genes which can be classified as oncogens or are in someway benificial to the survival of the tumor.
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array; Expression profiling by array; SNP genotyping by SNP array
Platforms:
GPL6947 GPL6985
68 Samples
Download data: TXT
Series
Accession:
GSE32964
ID:
200032964
17.

Molecular profiling of primary lung carcinomas

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by genome tiling array
Platforms:
GPL6947 GPL4723
150 Samples
Download data: GPR
Series
Accession:
GSE29066
ID:
200029066
18.

Landscape of somatic allelic imbalances and copy number alterations in human lung carcinoma

(Submitter supplied) Lung cancer is the worldwide leading cause of death from cancer. This GEO series correspond to one of the BAC aCGH data sets used as validation cohort for the study: Landscape of somatic allelic imbalances and copy number alterations in human lung cancer, Int J Cancer 2013.
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL4723
78 Samples
Download data: GPR, XLS
Series
Accession:
GSE29065
ID:
200029065
19.

Gene expression profiles of tumor and paired normal lung tissues from primary non-small cell lung cancer (NSCLC) patients in Taiwan.

(Submitter supplied) Genome-wide expression profiling of NSCLC patients were done using Phalanx Human OneArray chip. The surgically resected tumor tissue and corresponding normal tissue were collected from 21 patients diagnosed with primary NSCLC admitted to Taipei Veterans General Hospital, Taiwan.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6254
42 Samples
Download data: GPR
Series
Accession:
GSE21933
ID:
200021933
20.

Novel Lung Cancer-Related Genes Identified by a Non-Gapped Array-Comparative Genomic Hybridization Microarray in Asian and Caucasian Populations

(Submitter supplied) This study constructed a non-gapped bacterial artificial chromosomes (BAC) array containing 3604 BAC clones covering 18 lung cancer-related chromosome imbalance hotspot regions. Using this specialized array, DNA from tumor and normal tissues of 40 Asian and 20 Caucasian non-small cell lung cancer (NSLCL) patients was analyzed by array-comparative genomic hybridization (array-CGH). Block-wise normalization and a Bayes regression approach were used to refine the chromosomal imbalance regions identified by array-CGH. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL10303
60 Samples
Download data: GPR
Series
Accession:
GSE21276
ID:
200021276
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