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Links from GEO DataSets

Items: 20

1.

Copy number alteration in Murine Tumor Cells: primary inoculated tumor cells vs. out-growing tumor cells [Fig3b]

(Submitter supplied) Copy number alteration in out-growing mouse tumor cells comparing that in the original tumor cells that was primarily inoculated into the indicated mice. Goal is to determine the effects of IFN-gamma producing tumor-specific CTL on targeted tumor cell gene expression.
Organism:
Mus musculus
Type:
Genome variation profiling by genome tiling array
Platform:
GPL10449
10 Samples
Download data: TXT
Series
Accession:
GSE92266
ID:
200092266
2.

Copy number alteration in Murine Tumor Cells: primary inoculated tumor cells vs. out-growing tumor cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome variation profiling by genome tiling array
Platform:
GPL10449
63 Samples
Download data: TXT
Series
Accession:
GSE92271
ID:
200092271
3.

Copy number alteration in Murine Tumor Cells: primary inoculated tumor cells vs. out-growing tumor cells [Fig8b]

(Submitter supplied) Copy number alteration in out-growing mouse tumor cells comparing that in the original tumor cells that was primarily inoculated into the indicated mice. Goal is to determine the effects of IFN-gamma producing tumor-specific CTL on targeted tumor cell gene expression.
Organism:
Mus musculus
Type:
Genome variation profiling by genome tiling array
Platform:
GPL10449
6 Samples
Download data: TXT
Series
Accession:
GSE92270
ID:
200092270
4.

Copy number alteration in Murine Tumor Cells: primary inoculated tumor cells vs. out-growing tumor cells [Fig7b]

(Submitter supplied) Copy number alteration in out-growing mouse tumor cells comparing that in the original tumor cells that was primarily inoculated into the indicated mice. Goal is to determine the effects of IFN-gamma producing tumor-specific CTL on targeted tumor cell gene expression.
Organism:
Mus musculus
Type:
Genome variation profiling by genome tiling array
Platform:
GPL10449
10 Samples
Download data: TXT
Series
Accession:
GSE92269
ID:
200092269
5.

Copy number alteration in Murine Tumor Cells: primary inoculated tumor cells vs. out-growing tumor cells [Fig5b]

(Submitter supplied) Copy number alteration in out-growing mouse tumor cells comparing that in the original tumor cells that was primarily inoculated into the indicated mice. Goal is to determine the effects of IFN-gamma producing tumor-specific CTL on targeted tumor cell gene expression.
Organism:
Mus musculus
Type:
Genome variation profiling by genome tiling array
Platform:
GPL10449
8 Samples
Download data: TXT
Series
Accession:
GSE92268
ID:
200092268
6.

Copy number alteration in Murine Tumor Cells: primary inoculated tumor cells vs. out-growing tumor cells [Fig5a]

(Submitter supplied) Copy number alteration in out-growing mouse tumor cells comparing that in the original tumor cells that was primarily inoculated into the indicated mice. Goal is to determine the effects of IFN-gamma producing tumor-specific CTL on targeted tumor cell gene expression.
Organism:
Mus musculus
Type:
Genome variation profiling by genome tiling array
Platform:
GPL10449
9 Samples
Download data: TXT
Series
Accession:
GSE92267
ID:
200092267
7.

Copy number alteration in Murine Tumor Cells: primary inoculated tumor cells vs. out-growing tumor cells [Fig3a-b]

(Submitter supplied) Copy number alteration in out-growing mouse tumor cells comparing that in the original tumor cells that was primarily inoculated into the indicated mice. Goal is to determine the effects of IFN-gamma producing tumor-specific CTL on targeted tumor cell gene expression.
Organism:
Mus musculus
Type:
Genome variation profiling by genome tiling array
Platform:
GPL10449
10 Samples
Download data: TXT
Series
Accession:
GSE92265
ID:
200092265
8.

Copy number alteration in Murine Tumor Cells: primary inoculated tumor cells vs. out-growing tumor cells [Fig3a-a]

(Submitter supplied) Copy number alteration in out-growing mouse tumor cells comparing that in the original tumor cells that was primarily inoculated into the indicated mice. Goal is to determine the effects of IFN-gamma producing tumor-specific CTL on targeted tumor cell gene expression.
Organism:
Mus musculus
Type:
Genome variation profiling by genome tiling array
Platform:
GPL10449
10 Samples
Download data: TXT
Series
Accession:
GSE92264
ID:
200092264
9.

Gene-expression profiles of ovarian cancer regarding its microenvironment

(Submitter supplied) PD-L1 suppresses host immunity and promotes tumor growth. We investigated how IFN-γ regulates PD-L1 in the ovarian cancer microenvironment. In clinical samples, the number of stromal CTLs in peritoneally disseminated tumors was correlated with PD-L1 expression on the tumor cells, and the lymphocyte number was significantly related to the IFN-γ signature score. In mouse models, PD-L1 was induced in peritoneal disseminated tumors, where lymphocytes were prominent, but not in subcutaneous tumors. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
12 Samples
Download data: CEL
Series
Accession:
GSE55512
ID:
200055512
10.

Gene-expression profiles of IFN-gamma-affected HOSE cells

(Submitter supplied) The source of IFN-γ in ovarian cancer microenvironment and its biological effect to the tumor cells is unclear. The immortalized human ovarian surface epithelial cell line, HOSE-E7/hTERT (HOSE) was treated with IFN-γ and expression microarray analysis was performed, and probes showing significantly higher values in IFN-γ-added group were termed “IFN-γ signature genes (295 probes)”. We then applied this signature to our ovarian cancer microarray data, which included 75 ovarian cancer clinical samples, by means of ss-GSEA. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
8 Samples
Download data: CEL
Series
Accession:
GSE55510
ID:
200055510
11.

Functional genomic landscape of cancer-intrinsic immune evasion to cytotoxic T lymphocyte killing [CRISPRseq]

(Submitter supplied) The genetic circuits that allow cancer cells to evade destruction by the host immune system remain poorly understood. To identify a phenotypically robust core set of genes and pathways that facilitate cancer cell-intrinsic evasion to cytotoxic T lymphocyte (CTL)-mediated killing, we performed genome-wide CRISPR screens across a panel of genetically diverse cancer models cultured in the presence of CTLs. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL17021
46 Samples
Download data: TXT
Series
Accession:
GSE153397
ID:
200153397
12.

Functional genomic landscape of cancer-intrinsic immune evasion to cytotoxic T lymphocyte killing

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL17021 GPL19057 GPL24247
311 Samples
Download data: TXT
Series
Accession:
GSE149936
ID:
200149936
13.

Functional genomic landscape of cancer-intrinsic immune evasion to cytotoxic T lymphocyte killing [RNA-seq II]

(Submitter supplied) The genetic circuits that allow cancer cells to evade destruction by the host immune system remain poorly understood. To identify a phenotypically robust core set of genes and pathways that facilitate cancer cell-intrinsic evasion to cytotoxic T lymphocyte (CTL)-mediated killing, we performed genome-wide CRISPR screens across a panel of genetically diverse cancer models cultured in the presence of CTLs. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
78 Samples
Download data: TXT
Series
Accession:
GSE149935
ID:
200149935
14.

Functional genomic landscape of cancer-intrinsic immune evasion to cytotoxic T lymphocyte killing [RNA-seq I]

(Submitter supplied) The genetic circuits that allow cancer cells to evade destruction by the host immune system remain poorly understood. To identify a phenotypically robust core set of genes and pathways that facilitate cancer cell-intrinsic evasion to cytotoxic T lymphocyte (CTL)-mediated killing, we performed genome-wide CRISPR screens across a panel of genetically diverse cancer models cultured in the presence of CTLs. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL19057 GPL24247
12 Samples
Download data: TXT
Series
Accession:
GSE149934
ID:
200149934
15.

Functional genomic landscape of cancer-intrinsic immune evasion to cytotoxic T lymphocyte killing [CRISPR screen]

(Submitter supplied) The genetic circuits that allow cancer cells to evade destruction by the host immune system remain poorly understood. To identify a phenotypically robust core set of genes and pathways that facilitate cancer cell-intrinsic evasion to cytotoxic T lymphocyte (CTL)-mediated killing, we performed genome-wide CRISPR screens across a panel of genetically diverse cancer models cultured in the presence of CTLs. more...
Organism:
Mus musculus
Type:
Other
Platforms:
GPL17021 GPL19057
175 Samples
Download data: TXT
Series
Accession:
GSE149933
ID:
200149933
16.

Single-cell RNA-sequencing of murine melanoma infiltrating immune cells in wild-type and miR-155 T cell conditional knockout mice

(Submitter supplied) miR-155 has recently emerged as an important promoter of antitumor immunity through its functions in T lymphocytes. However, the impact of T cell expressed miR-155 on immune cell dynamics in solid tumors remains unclear. In the present study, we used single-cell RNA-sequencing to define the CD45+ immune cell populations within B16F10 murine melanoma tumors growing in either wild-type (WT) or miR-155 T cell conditional knockout (TCKO) mice at different timepoints. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: MTX, TSV
Series
Accession:
GSE121478
ID:
200121478
17.

Noncoding regions are the main source of targetable tumor-specific antigens

(Submitter supplied) Purpose: Tumor-specific antigens (TSAs) represent ideal targets for cancer immunotherapy, but very few of them have been identified. Therefore, the goal of this study was to develop a novel approach, combining RNA-Sequencing and mass spectrometry, to enlarge the landscape of actionable TSAs in seven human primary samples, namely 4 B-ALL and 3 lung tumor biopsies.  Methods: We performed RNA-Sequencing on each primary tumor sample (unreplicated) with the Illumina HiSeq200. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
6 Samples
Download data: TXT
18.

Non-coding regions are the main source of tumor-specific antigens

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL19057 GPL11154 GPL13112
15 Samples
Download data: TSV
Series
Accession:
GSE113992
ID:
200113992
19.

Non-coding regions are the main source of tumor-specific antigens [human]

(Submitter supplied) Purpose: Tumor-specific antigens (TSAs) represent ideal targets for cancer immunotherapy, but very few of them have been identified. Therefore, the goal of this study was to develop a novel approach, combining RNA-Sequencing and mass spectrometry, to enlarge the landscape of actionable TSAs in seven human primary samples, namely 4 B-ALL and 3 lung tumor biopsies. Methods: We performed RNA-Sequencing on each primary tumor sample (unreplicated) with the Illumina HiSeq2000. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
7 Samples
Download data: TSV
Series
Accession:
GSE113972
ID:
200113972
20.

Non-coding regions are the main source of tumor-specific antigens [mouse]

(Submitter supplied) Purpose: Tumor-specific antigens (TSAs) represent ideal targets for cancer immunotherapy, but very few of them have been identified. Therefore, the goal of this study was to develop a novel approach, combining RNA-Sequencing and mass spectrometry, to enlarge the landscape of actionable TSAs in two murine cell lines, namely EL4 and CT26 cells. Methods: We performed RNA-Sequencing on both tumor cell lines (unreplicated) as well as on the syngeneic mature medullary thymic epithelial cells (mTEChi, in triplicate), using either the Illumina HiSeq200 or the Illumina NextSeq 500. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL13112 GPL19057
8 Samples
Download data: TSV
Series
Accession:
GSE111092
ID:
200111092
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