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Items: 1 to 20 of 65

1.

Drug sensitivity screening and genomic characterization of 45 HPV-negative head and neck carcinoma cell lines for novel biomarkers of drug efficacy

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below. GSE107918 GSE108061
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array; Expression profiling by array
Platforms:
GPL10558 GPL9128
90 Samples
Download data: IDAT, TXT
Series
Accession:
GSE108062
ID:
200108062
2.

Drug sensitivity screening and genomic characterization of 45 HPV-negative head and neck carcinoma cell lines for novel biomarkers of drug efficacy [CGH]

(Submitter supplied) There is an unmet need for effective targeted therapies for patients with advanced head and neck squamous cell carcinoma (HNSCC). We correlated gene expression, gene copy numbers, and point mutations in 45 human papillomavirus-negative HNSCC cell lines with the sensitivity to 220 anticancer drugs to discover predictive associations to genetic alterations. The drug response profiles revealed diverse efficacy of the tested drugs across the cell lines. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9128
45 Samples
Download data: TXT
Series
Accession:
GSE107918
ID:
200107918
3.

Mapping alterations spatially and temporally during early stages of breast tumourigenesis

(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:
GPL6480 GPL9128
72 Samples
Download data: TXT
Series
Accession:
GSE72653
ID:
200072653
4.

Mapping alterations spatially and temporally during early stages of breast tumourigenesis [aCGH]

(Submitter supplied) Identifying genomic alterations that precede tumourigenesis of breast tumours will allow us to better understand tumour development and heterogeneity. In particular, by obtaining and profiling normal-epithelium samples at various distances from the tumour, we can draft both a spatial and temporal map of the genomic events and transcriptomic alterations that occur along the mammary duct (leading up to and including the tumour).
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9128
36 Samples
Download data: TXT
Series
Accession:
GSE72652
ID:
200072652
5.

Copy number profiling of 5-FU resistant gastric cancer cell line compared to the parental cell line

(Submitter supplied) Copy number profiling of MKN45T 5-FU resistant gastric cancer cell lines and its parental cell line MKN45. We hypothesized that a detailed fine-scale survey of genomic CNAs might reveal the mechanism for acquired resistant to 5-FU in gastric cancer.
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9128
1 Sample
Download data: TXT
Series
Accession:
GSE89191
ID:
200089191
6.

Genomic copy number aberrations in multiple synchronous lung cancer.

(Submitter supplied) In current study, we applied array-CGH analysis to detect somatic copy number aberrations across tumor genome to help separate multiple primary lung cancers from metastasis cancers.
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9128
23 Samples
Download data: TXT
Series
Accession:
GSE86607
ID:
200086607
7.

Genomic profiling of 49 gastric cancer cell lines by array-based comparative genomic hybridization

(Submitter supplied) In this study, we investigated amplifications and deletions of 49 gastric cancer cell lines by 244k oligonucleotide-based array comparative genomic hybridization.
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9128
49 Samples
Download data: TXT
Series
Accession:
GSE74839
ID:
200074839
8.

Genomic copy number aberrations of 11 gastric cancer cell lines

(Submitter supplied) Genomic copy number aberrations of 11 gastric cancer cell lines were analyzed by 244k CGH array from Agilent Technologies. Based on this results, we separated the 11 cell lines into 2 groups, with and without copy number increase at chromosome 20q13
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9128
11 Samples
Download data: TXT
Series
Accession:
GSE67604
ID:
200067604
9.

Genomic profiling of IPMN with an associated invasive carcinomas (IPMN-inv) and invasive ductal carcinomas (IDC) by array-based comparative genomic hybridization

(Submitter supplied) In this study, we aimed to identify gene abnormalities necessary for the transformation from carcinoma in situ (CIS) of pancreas to invasive PC. We compared the genomic profiles of paired samples from invasive region and CIS region of the identical IPMN-inv. We further determined genomic profiles of IDC.
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL9128
39 Samples
Download data: TXT, XLSX
Series
Accession:
GSE65181
ID:
200065181
10.

Translational compensation of genomic instability in neuroblastoma

(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; Non-coding RNA profiling by array
Platforms:
GPL6480 GPL9128 GPL8227
50 Samples
Download data: TXT
Series
Accession:
GSE56656
ID:
200056656
11.

aCGH profiling of MYCN-amplified Neuroblastoma cell lines

(Submitter supplied) Genome copy-number status has been profiled on 13 MYCN-amplified Neuroblastoma cell lines
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9128
13 Samples
Download data: TXT
Series
Accession:
GSE56654
ID:
200056654
12.

Squamous cell carcinoma of the lung

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array; Expression profiling by array
Platforms:
GPL6480 GPL9128
48 Samples
Download data: TXT
Series
Accession:
GSE40089
ID:
200040089
13.

Agilent 244A aCGH array for squamous cell carcinoma of the lung

(Submitter supplied) 24 SCC tumors were profiled for copy-number alterations with the high-resolution Agilent 244A aCGH Array
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9128
24 Samples
Download data: TXT
Series
Accession:
GSE40048
ID:
200040048
14.

Drug screening and genomic analyses of HER2 positive breast cancer cell lines reveal predictors for treatment response

(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:
GPL18850 GPL9128
17 Samples
Download data: CEL, TXT
Series
Accession:
GSE58887
ID:
200058887
15.

Drug screening and genomic analyses of HER2 positive breast cancer cell lines reveal predictors for treatment response [CGH]

(Submitter supplied) Thirteen HER2 positive breast cancer cell lines were screened with 22 commercially available compounds, mainly targeting proteins in the ErbB2 signaling pathway, and the molecular mechanisms related to treatment response were sought. To search for response predictors, genomic and transcriptomic profiling, PIK3CA mutations and PTEN status were associated to the drug responses and several genes involved in the response of the compounds were identified. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9128
4 Samples
Download data: TXT
Series
Accession:
GSE58886
ID:
200058886
16.

Somatic copy number alterations associated with populations and clinical characteristics in ovarian clear cell adenocarcinoma

(Submitter supplied) Background: Clinical characteristics of ovarian clear cell adenocarcinoma (CCC) include 1) higher incidence among Japanese, 2) association with endometriosis, 3) poor prognosis in advanced stage, 4) higher incidence of thrombosis as complication. We applied high resolution comparative genomic hybridization (CGH) array to screen somatic copy number alterations (SCNAs) associated with these clinical characteristics. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9128
117 Samples
Download data: TXT
Series
Accession:
GSE58342
ID:
200058342
17.

Hepatosplenic T cell lymphoma

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Expression profiling by high throughput sequencing; Genome variation profiling by SNP array; Genome variation profiling by genome tiling array
4 related Platforms
24 Samples
Download data: CEL, CYCHP, TXT
Series
Accession:
GSE57944
ID:
200057944
18.

aCGH data of 5 cases of Hepatosplenic T-cell lymphoma

(Submitter supplied) Hepatosplenic T-cell lymphoma (HSTL) is an aggressive lymphoma cytogenetically characterized by isochromosome 7q [i(7)(q10)], of which the molecular consequences remain unknown. We report here results of an integrative genomic and transcriptomic (expression microarray and RNA-sequencing) study of six HSTL cases with i(7)(q10) and three cases with ring 7 [r(7)], a rare variant aberration. Using high resolution array CGH, we prove that HSTL is characterized by the common loss of a 34.88 Mb region at 7p22.1p14.1 (3506316-38406226 bp) and duplication/amplification of a 38.77 Mb region at 7q22.11q31.1 (86259620-124892276 bp). more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9128
5 Samples
Download data: TXT
Series
Accession:
GSE57942
ID:
200057942
19.

Follicular lymphoma in situ and partial involvement by follicular lymphoma are clona lesions that carry the t(14;18) and lack genetic secondary alterations

(Submitter supplied) Follicular lymphoma (FL) is characterized by the t(14;18)(q32;q21), frequent numerical chromosomal alterations, and recurrent somatic mutations. However, no genetic studies are available for FL in situ (FLIS), a putative precursor lesion of FL. In this study, we analyzed cases of FLIS without manifest (m)FL, partial involvement by FL (PFL), and paired cases of FLIS and mFL to detect possible early chromosomal imbalances, as well as DNA-methylation patterns of genomic regions of selected genes. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL9128
20 Samples
Download data: TXT
Series
Accession:
GSE48548
ID:
200048548
20.

Drug Synergy Screen and Network Modeling in Dedifferentiated Liposarcoma (DDLS)

(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:
GPL9128 GPL6947
8 Samples
Download data: TXT
Series
Accession:
GSE50751
ID:
200050751
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