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Links from GEO DataSets

Items: 20

1.

Affymetrix SNP array data for Sézary Syndrome (SS) samples

(Submitter supplied) This study used tumour and paired normal samples from 28 Sézary Syndrome (SS) patients to define recurrent regions of chromosomal aberrations. Our data identified recurrent losses of 17p13.2-p11.2 and 10p12.1-q26.3 occurring in 71 and 68% of cases respectively; common gains were detected for 17p11.2-q25.3 (64%) and chromosome 8/8q (50%). Moreover, we identified novel genomic lesions recurring in more than 30% of tumours: loss of 9q13-q21.33 and gain of 10p15.3-10p12.2. more...
Organism:
Homo sapiens
Type:
SNP genotyping by SNP array; Genome variation profiling by SNP array
Platforms:
GPL1266 GPL2641
56 Samples
Download data: CEL
Series
Accession:
GSE17595
ID:
200017595
2.

Identification of regions and genes important in Sézary syndrome pathogenesis using genomic and expression microarrays

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
SNP genotyping by SNP array; Genome variation profiling by SNP array; Expression profiling by array
Platforms:
GPL1266 GPL96 GPL2641
88 Samples
Download data: CEL
Series
Accession:
GSE17602
ID:
200017602
3.

Affymetrix Gene Expression array data for Sézary Syndrome (SS) samples

(Submitter supplied) This study used tumour and paired normal samples from 28 Sézary Syndrome (SS) patients to define recurrent regions of chromosomal aberrations. Our data identified recurrent losses of 17p13.2-p11.2 and 10p12.1-q26.3 occurring in 71 and 68% of cases respectively; common gains were detected for 17p11.2-q25.3 (64%) and chromosome 8/8q (50%). Moreover, we identified novel genomic lesions recurring in more than 30% of tumours: loss of 9q13-q21.33 and gain of 10p15.3-10p12.2. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
32 Samples
Download data: CEL
Series
Accession:
GSE17601
ID:
200017601
4.

Novel and highly recurrent chromosomal alterations in Sézary syndrome

(Submitter supplied) This study was designed to identify highly recurrent genetic alterations typical of Sézary syndrome (Sz), an aggressive cutaneous T-cell lymphoma/leukemia, possibly revealing pathogenetic mechanisms and novel therapeutic targets. High-resolution array-based comparative genomic hybridization was done on malignant T cells from 20 patients. Expression levels of selected biologically relevant genes residing within loci with frequent copy number alteration were measured using quantitative PCR. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL8634
20 Samples
Download data: GPR
Series
Accession:
GSE16384
ID:
200016384
5.

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
6.

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
7.

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
8.

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
9.

Genome-wide multi-omics profiling reveals extensive genetic complexity in 8p11-p12 amplified breast carcinomas [expression]

(Submitter supplied) Transcriptomic profiling of human breast tumors. Genomic and expression profiling using 38K BAC array-CGH and Illumina HT-12 beadchips were performed on 53 invasive breast tumors to assess the impact of gene dosage on gene expression patterns and the effect of other mechanisms on transcriptional levels. Array-CGH results was validated by FISH using tumors showing 8p11-p12 DNA amplification and expression profiling was confirmed using qPCR for 11 transcripts. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6947
53 Samples
Download data: IDAT, TXT
Series
Accession:
GSE97177
ID:
200097177
10.

Clinical implications of gene dosage and gene expression patterns in diploid breast carcinoma

(Submitter supplied) Genomic and expression profiling using 38K BAC array-CGH and Illumina HT-12 beadchips were performed on 97 diploid invasive breast tumors to assess the impact of gene dosage on gene expression patterns and the effect of other mechanisms on transcriptional levels. Patient stratification was performed according to axillary lymph node status (node-negative, pN0; node-positive, pN1) and overall survival (>8-year survivors; breast cancer-specific mortality within 8 years of diagnosis). more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by array
Platforms:
GPL6947 GPL9077
194 Samples
Download data: CSV, GPR, IDAT
Series
Accession:
GSE20486
ID:
200020486
11.

Clinical implications of gene dosage and gene expression patterns in diploid breast carcinoma (CGH)

(Submitter supplied) Genomic and expression profiling using 38K BAC array-CGH and Illumina HT-12 beadchips were performed on 97 diploid invasive breast tumors to assess the impact of gene dosage on gene expression patterns and the effect of other mechanisms on transcriptional levels. Patient stratification was performed according to axillary lymph node status (node-negative, pN0; node-positive, pN1) and overall survival (>8-year survivors; breast cancer-specific mortality within 8 years of diagnosis). more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL9077
97 Samples
Download data: GPR
Series
Accession:
GSE20483
ID:
200020483
12.

Clinical implications of gene dosage and gene expression patterns in diploid breast carcinoma (transcriptomic profiling)

(Submitter supplied) Genomic and expression profiling using 38K BAC array-CGH and Illumina HT-12 beadchips were performed on 97 diploid invasive breast tumors to assess the impact of gene dosage on gene expression patterns and the effect of other mechanisms on transcriptional levels. Patient stratification was performed according to axillary lymph node status (node-negative, pN0; node-positive, pN1) and overall survival (>8-year survivors; breast cancer-specific mortality within 8 years of diagnosis). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6947
97 Samples
Download data: CSV, IDAT, TXT
Series
Accession:
GSE20462
ID:
200020462
13.

Affymetrix 250K StyI SNP array data from PBMCs and cell lines of metastatic melanoma patients

(Submitter supplied) Allele call files from on 250K StyI SNP array using DNA from 60 human cell lines from metastasized melanoma and from 44 corresponding peripheral blood mononuclear cells (CEL and CHP files provided).
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array; SNP genotyping by SNP array
Platform:
GPL3720
104 Samples
Download data: CEL, CHP
Series
Accession:
GSE17534
ID:
200017534
14.

SNP array genomic profiling of PTCL NOS

(Submitter supplied) DNA extracted from frozen tissue of 47 peripheral T-cell lymphomas–not otherwise specified [PTCL-NOS] was hybridized to 250k StyI SNP arrays
Organism:
Homo sapiens
Type:
SNP genotyping by SNP array; Genome variation profiling by SNP array
Platform:
GPL3720
67 Samples
Download data: CEL, CHP
Series
Accession:
GSE15842
ID:
200015842
15.

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
16.

Effect of genomic imbalances on gene expression in rhabdomyosarcoma

(Submitter supplied) Rhabdomyosarcoma (RMS) is the most common paediatric soft-tissue sarcoma and resembles developing skeletal muscle. Specific genomic alterations including translocations, deletions and amplification events have been associated with the alveolar and embryonal subtypes of RMS. Characterizing these changes has led to increased understanding of the underlying molecular biology. However, further aberrations and their significance remain to be defined. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
13 Samples
Download data: CEL, CHP
Series
Accession:
GSE8840
ID:
200008840
17.

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 GPL7394 GPL5477
28 Samples
Download data
Series
Accession:
GSE12951
ID:
200012951
18.

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
19.

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
20.

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
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