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Links from GEO DataSets

Items: 20

1.

Paired copy number analysis of Diffuse Large B Cell Lymphoma [OncoScan]

(Submitter supplied) Copy number analysis can be useful for assessing prognosis in diffuse large B cell lymphoma (DLBCL). We analyzed copy number data from tumor samples of 60 patients diagnosed with DLBCL de novo and their matched normal samples. We detected a total of 63 recurrent copy number alterations (CNAs), including 33 gains, 30 losses, and nine recurrent acquired copy number neutral loss of heterozygosity (CNN-LOH). more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL18602
38 Samples
Download data: CEL, TXT, XLS
Series
Accession:
GSE71386
ID:
200071386
2.

Paired copy number analysis of Diffuse Large B Cell Lymphoma

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome variation profiling by array; Genome variation profiling by SNP array
Platforms:
GPL15315 GPL18602
100 Samples
Download data: CEL
Series
Accession:
GSE71394
ID:
200071394
3.

Paired copy number analysis of DLBCL Diffuse Large B Cell Lymphoma [SNP 6.0 Array]

(Submitter supplied) Copy number analysis can be useful for assessing prognosis in diffuse large B cell lymphoma (DLBCL). We analyzed copy number data from tumor samples of 60 patients diagnosed with DLBCL de novo and their matched normal samples. We detected a total of 63 recurrent copy number alterations (CNAs), including 33 gains, 30 losses, and nine recurrent acquired copy number neutral loss of heterozygosity (CNN-LOH). more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platform:
GPL15315
62 Samples
Download data: CEL, TXT
Series
Accession:
GSE71389
ID:
200071389
4.

Characterization of genomic imbalances in diffuse large B-cell lymphoma by high resolution SNP-chip analysis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by SNP array; SNP genotyping by SNP array
Platforms:
GPL96 GPL3720
296 Samples
Download data: CEL, CHP
Series
Accession:
GSE57612
ID:
200057612
5.

HGU133A expression array data for diffuse large B cell lymphoma samples

(Submitter supplied) The pathogenesis of diffuse large B cell lymphomas (DLBCL) is only partly understood. We analyzed 148 DLBCL by high resolution single nucleotide polymorphism (SNP)-chips to characterize genomic imbalances. Seventy-nine cases were of the germinal center B-cell like (GCB) type of DLBCL, 49 of the activated B-cell like (ABC) subtype and 20 were type 3 DLBCL. Twenty-four regions of recurrent genomic gains and 38 regions of recurrent genomic losses were identified over the whole cohort, with a median of 25 imbalances per case for ABC-DLBCL and 19 per case for GCB-DLBCL. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
148 Samples
Download data: CEL
Series
Accession:
GSE57611
ID:
200057611
6.

Affymetrix SNP array data for diffuse large B cell lymphoma samples

(Submitter supplied) The pathogenesis of diffuse large B cell lymphomas (DLBCL) is only partly understood. We analyzed 148 DLBCL by high resolution single nucleotide polymorphism (SNP)-chips to characterize genomic imbalances. Seventy-nine cases were of the germinal center B-cell like (GCB) type of DLBCL, 49 of the activated B-cell like (ABC) subtype and 20 were type 3 DLBCL. Twenty-four regions of recurrent genomic gains and 38 regions of recurrent genomic losses were identified over the whole cohort, with a median of 25 imbalances per case for ABC-DLBCL and 19 per case for GCB-DLBCL. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array; SNP genotyping by SNP array
Platform:
GPL3720
148 Samples
Download data: CEL, CHP
Series
Accession:
GSE57277
ID:
200057277
7.

Comparative whole genome profiling of post-transplant lymphoproliferative disorders and diffuse large B-cell lymphomas.

(Submitter supplied) Post-transplant lymphoproliferative disorders (PTLD) are a major complication of solid organ transplantation and represent a cause of severe morbidity and mortality among transplanted patients. Apart from EBV infection, knowledge of the pathogenesis of monoclonal PTLD is limited. Powerful analysis techniques, such as whole genomic DNA profiling (arrayCGH), can improve our understanding of PTLD pathogenesis. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array; SNP genotyping by SNP array
Platform:
GPL2641
45 Samples
Download data: CEL
Series
Accession:
GSE8123
ID:
200008123
8.

Enhanced DNA repair and genomic stability identify a novel HIV related Diffuse Large B-cell Lymphoma subtype

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Other; Genome variation profiling by array
Platforms:
GPL19387 GPL25534
79 Samples
Download data: RCC, TXT
Series
Accession:
GSE119537
ID:
200119537
9.

Enhanced DNA repair and genomic stability identify a novel HIV related Diffuse Large B-cell Lymphoma subtype [aCGH]

(Submitter supplied) Transcriptional and genomic profiling study of HIV positive and HIV negative Diffuse Large B-Cell Lymphoma (DLBCL). Tumors were subtyped using the Lymph2Cx assay. Only GCB (germinal center like B-cell) subtypes were then subjected to digitial gene expression profiling and array comparative genomic hybridization (aCGH). The study used DNA extracted from FFPE DLBCL tumors derived from HIV(+) and HIV(-) patients to assess copy number variation differences between the HIV(+) and HIV(-) cohorts. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL19387
39 Samples
Download data: TXT
Series
Accession:
GSE119536
ID:
200119536
10.

Enhanced DNA repair and genomic stability identify a novel HIV related Diffuse Large B-cell Lymphoma subtype [nanostring]

(Submitter supplied) Transcriptional and genomic profiling study of HIV positive and HIV negative Diffuse Large B-Cell Lymphoma (DLBCL). Tumors were subtyped using the Lymph2Cx assay. Only GCB (germinal center like B-cell) subtypes were then subjected to digitial gene expression profiling and array comparative genomic hybridization (aCGH). The study used total RNA extracted from FFPE DLBCL tumors derived from HIV(+) and HIV(-) patients to assess differential expression of known cancer genes. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL25534
40 Samples
Download data: RCC, TXT
Series
Accession:
GSE119534
ID:
200119534
11.

Integration of transcript expression, copy number and LOH analysis of infiltrating ductal carcinoma of the breast

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by SNP array
Platforms:
GPL570 GPL3720
42 Samples
Download data: CEL
Series
Accession:
GSE22840
ID:
200022840
12.

Integration of transcript expression, copy number and LOH analysis of infiltrating ductal carcinoma of the breast: copy number analysis

(Submitter supplied) Introduction: A major challenge in the interpretation of genomic profiling data generated from breast cancer samples is the identification of driver genes as distinct from bystander genes which do not impact tumorigenesis. One way to assess the relative importance of alterations in the transcriptome profile is to combine complementary analyses that assess changes in the copy number alterations (CNAs). more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platform:
GPL3720
22 Samples
Download data: CEL
Series
Accession:
GSE22839
ID:
200022839
13.

Integration of transcript expression, copy number and LOH analysis of infiltrating ductal carcinoma of the breast: expression analysis

(Submitter supplied) Introduction: A major challenge in the interpretation of genomic profiling data generated from breast cancer samples is the identification of driver genes as distinct from bystander genes which do not impact tumorigenesis. One way to assess the relative importance of alterations in the transcriptome profile is to combine complementary analyses that assess changes in the copy number alterations (CNAs). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
20 Samples
Download data: CEL
Series
Accession:
GSE22544
ID:
200022544
14.

Expression data from Diffuse Large B Cell Lymphoma (DLBCL) patients

(Submitter supplied) Diffuse large B-cell lymphoma (DLBCL) is currently divided into three main molecular subtypes, defined by gene expression profiling (GEP): Germinal Center B-cell like (GCB), Activated B-Cell like (ABC), and Primary Mediastinal B-cell Lymphoma (PMBL). DLBCL subtypes were determined according to patients' gene expression profiles.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
223 Samples
Download data: CEL
Series
Accession:
GSE87371
ID:
200087371
15.

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
16.

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
17.

Genomic alterations and gene expression in primary diffuse large B cell lymphomas of immune privileged sites

(Submitter supplied) Primary diffuse large B cell lymphomas of different immune-privileged sites (IP-DLBCL) share many clinical and biological features, such as a relatively poor prognosis, preferential dissemination to other immune-privileged sites and deletion of the HLA region, which suggests that IP-DLBCL represents a separate entity. To further investigate the nature of IP-DLBCL, we investigated site-specific genomic aberrations in 16 testicular, 9 central nervous system (CNS) and 15 nodal DLBCL using array-CGH. more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by genome tiling array
Platforms:
GPL4012 GPL570
80 Samples
Download data: CEL, CHP, GPR
Series
Accession:
GSE10524
ID:
200010524
18.

Integrating genomic alterations in diffuse large B-cell Lymphoma identifies new relevant pathways and potential therapeutic targets

(Submitter supplied) Genome studies of diffuse large B-cell lymphoma (DLBCL) have revealed a large number of somatic mutations and structural alterations that may contribute to their heterogeneous behavior. However, their clinical relevance and potential interest in identifying appropriate candidate drugs for personalized management are not well known. In this study, targeted next generation sequencing and genomic copy number alterations (CNA) were analyzed in 150 cases of diffuse large B-cell lymphoma (DLBCL) to define the clinical significance of recurrent genomic alterations and to identify potential targets for personalized management. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platform:
GPL16131
119 Samples
Download data: CEL, CYCHP, XLSX
Series
Accession:
GSE94705
ID:
200094705
19.

Expression data and Copy Number Variations from Diffuse Large B Cell Lymphoma (DLBCL) patients

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL27429 GPL570
448 Samples
Download data: CEL, TXT
Series
Accession:
GSE136971
ID:
200136971
20.

Copy Number Variations identified in 225 Diffuse Large B-Cell Lymphoma tumors

(Submitter supplied) Copy Number Variations (CNVs) were identified performing Comparative Genomic Hybridization (CGH) on 225 patients after whole-genome amplification, using Agilent SurePrint G3 4x180K microarrays. CNVs were further integrated with gene expression (Affymetrix U133+2 arrays) and mutations (targeted DNA resequencing). Complete description of the methods, array quality checks and called segments are available as supplemental material in the corresponding publication.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL27429
225 Samples
Download data: TXT
Series
Accession:
GSE136962
ID:
200136962
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