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Links from GEO DataSets

Items: 20

1.

Clonal competition with alternating dominance in multiple myeloma

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome variation profiling by array; Expression profiling by array
Platforms:
GPL570 GPL4091 GPL2879
104 Samples
Download data: CEL, TXT
Series
Accession:
GSE36825
ID:
200036825
2.

Clonal competition with alternating dominance in multiple myeloma [GEP]

(Submitter supplied) Copy number and expression profiling of multiple myeloma patients at multiple stages of their individual clinical course Identification of evolutionary patterns in multiple myeloma
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
42 Samples
Download data: CEL
Series
Accession:
GSE36824
ID:
200036824
3.

Clonal competition with alternating dominance in multiple myeloma [44kCGH]

(Submitter supplied) Copy number and Gene expression profiling multiple myeloma patients at multiple stages of their individual clinical course Identification of evolutionary paterns in multiple myeloma
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL2879
7 Samples
Download data: TXT
Series
Accession:
GSE36823
ID:
200036823
4.

Clonal competition with alternating dominance in multiple myeloma [244kCGH]

(Submitter supplied) Copy number and Gene expression profiling multiple myeloma patients at multiple stages of their individual clinical course Identification of evolutionary paterns in multiple myeloma
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL4091
55 Samples
Download data: TXT
Series
Accession:
GSE36822
ID:
200036822
5.

A compendium of myeloma associated chromosomal copy number abnormalities and their prognostic value

(Submitter supplied) To obtain a comprehensive genomic profile of presenting multiple myeloma cases we performed high resolution single nucleotide polymorphism (SNP) mapping array analysis in 114 samples alongside 258 samples analysed by U133 Plus 2.0 expression array (Affymetrix). We examined DNA copy number alterations and loss of heterozygosity (LOH) in order to define the spectrum of minimally deleted regions in which relevant genes of interest can be found. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array; SNP genotyping by SNP array; Expression profiling by array
Platforms:
GPL570 GPL3720 GPL3718
491 Samples
Download data: CEL, CHP
Series
Accession:
GSE21349
ID:
200021349
6.

Hierarchy of mono- and bi-allelic TP53 alterations in Multiple Myeloma cell fitness

(Submitter supplied) Comparison of the TP53 wild-type myeloma cell line AMO1 with the CRISPR/Cas9 engineered AMO1 cell line named UMC901. UMC901 harbors bi-allelic alterations to TP53: TP53 del/mut. Analysis of impact of TP53 alterations on gene transcription and identification of affected pathways by transcriptome-wide differential gene expression analysis.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
6 Samples
Download data: CSV
Series
Accession:
GSE132340
ID:
200132340
7.

RNA-Seq, WGS, WXS of mouse myeloma tumors derived from Vk*MYC transgenic mice

(Submitter supplied) Comprehensive genomic analysis (WXS, WGS, RNAseq) identifies shared pathways of progression between human and mouse myeloma.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL24247
195 Samples
Download data: TXT, VCF
Series
Accession:
GSE255233
ID:
200255233
8.

Genome-wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with transcriptional Profile alterations

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array; SNP genotyping by SNP array; Expression profiling by array
Platforms:
GPL6244 GPL3718
38 Samples
Download data: CEL
Series
Accession:
GSE39383
ID:
200039383
9.

Genome-wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with transcriptional Profile alterations (Expression)

(Submitter supplied) Primary plasma cell leukaemia (pPCL) is a rare, yet aggressive form of de novo plasma cell tumor, distinguished from secondary PCL (sPCL) which represents a leukemic transformation of pre-existing multiple myeloma (MM). Here, we performed a comprehensive molecular analysis of a prospective series of pPCLs by means of FISH, single nucleotide polymorphism (SNP) array and gene expression profiling (GEP). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
21 Samples
Download data: CEL
Series
Accession:
GSE39381
ID:
200039381
10.

Genome-wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with transcriptional Profile alterations (Copy number)

(Submitter supplied) Primary plasma cell leukaemia (pPCL) is a rare, yet aggressive form of de novo plasma cell tumor, distinguished from secondary PCL (sPCL) which represents a leukemic transformation of pre-existing multiple myeloma (MM). Here, we performed a comprehensive molecular analysis of a prospective series of pPCLs by means of FISH, single nucleotide polymorphism (SNP) array and gene expression profiling (GEP). more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array; SNP genotyping by SNP array
Platform:
GPL3718
17 Samples
Download data: CEL
Series
Accession:
GSE39380
ID:
200039380
11.

Transcriptome analysis reveals significant differences between primary plasma cell leukemia and multiple myeloma even when sharing a similar genetic background

(Submitter supplied) Primary plasma cell leukemia (pPCL) is a highly aggressive plasma cell dyscrasia characterized by short remissions and very poor survival. Deletions of 17p13 are much more frequent in pPCL than in multiple myeloma (MM). Although the 17p deletion is associated with poor outcome and extramedullary disease in MM, its presence does not confer the degree of aggressiveness observed in pPCL. The comprehensive exploration of the transcriptome, including isoform expression and RNA splicing events, may provide novel information about biological differences between the two diseases carrying a 17p deletion. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL20932
19 Samples
Download data: CEL
Series
Accession:
GSE131216
ID:
200131216
12.

Clonal selection and double hit events involving tumor suppressor genes underlie relapse from chemotherapy: myeloma as a model

(Submitter supplied) To elucidate the mechanisms underlying relapse from chemotherapy in multiple myeloma we performed a longitudinal study of 33 patients entered into Total Therapy protocols investigating them using gene expression profiling, high resolution copy number arrays and whole exome sequencing. The study illustrates the mechanistic importance of acquired mutations in known myeloma driver genes and the critical nature of bi-allelic inactivation events affecting tumor suppressor genes, especially TP53. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
66 Samples
Download data: CEL
Series
Accession:
GSE82307
ID:
200082307
13.

Clonal evolution in relapsed NPM1 mutated acute myeloid leukemia

(Submitter supplied) Mutations in the nucleophosmin 1 (NPM1) gene are considered as a founder event in the pathogenesis of acute myeloid leukemia (AML). To address the role of clonal evolution in relapsed NPM1 mutated (NPM1mut) AML, we applied high-resolution genome-wide single-nucleotide polymorphism (SNP) array profiling to detect copy number alterations (CNA) and uniparental disomies (UPD) and performed comprehensive gene mutation screening in 53 paired bone marrow/peripheral blood samples obtained at diagnosis and relapse. more...
Organism:
Homo sapiens
Type:
SNP genotyping by SNP array
Platform:
GPL6801
159 Samples
Download data: CEL, CHP
Series
Accession:
GSE46951
ID:
200046951
14.

Clonal evolution in multiple myeloma after treatment pressure: heterogenous genomic aberrations and transcriptomic convergence

(Submitter supplied) Multiple myeloma (MM) is still an incurable plasma cell malignancy that generally responds well to treatment intitially, but eventually becomes refractory. In the present study, genomic and transcriptomic changes were investigated in paired early and late tumor samples of MM patients .
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL18573 GPL20301
51 Samples
Download data: TXT
Series
Accession:
GSE179929
ID:
200179929
15.

Plasma cell dyscrasias expression profiles associated with distinct IGH translocations in multiple myeloma

(Submitter supplied) This series of microarray experiments contains the gene expression profiles of purified plasma cells (PCs) obtained from 7 monoclonal gammopathy of undetermined significance (MGUS), 39 newly diagnosed multiple myeloma (MM) and 6 plasma-cell leukaemia (PCL) patients. PCs were purified from bone marrow Seriess, after red blood cell lysis with 0.86% ammonium chloride, using CD138 immunomagnetic microbeads. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1067
Platform:
GPL96
52 Samples
Download data: CEL
Series
Accession:
GSE2113
ID:
200002113
16.
Full record GDS1067

Plasma cell dyscrasias

Expression profiling of plasma cells from patients with plasma cell dyscrasias: 7 with monoclonal gammopathy of undetermined significance, 39 with multiple myeloma (MM), and 6 with plasma cell leukemia. Results provide insight into the neoplastic transformation of plasma cells in MM.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 disease state sets
Platform:
GPL96
Series:
GSE2113
52 Samples
Download data: CEL
DataSet
Accession:
GDS1067
ID:
1067
17.

Somatic mutation spectrum in monoclonal gammopathy of undetermined significance indicates a simpler genomic landscape compared to multiple myeloma

(Submitter supplied) Monoclonal gammopathy of undetermined significance (MGUS) is a premalignant precursor of multiple myeloma (MM) with a 1% risk of progression per year. Although targeted analyses have shown the presence of specific genetic abnormalities such as IGH translocations, RB1 deletion, 1q gain, hyperdiploidy or RAS genes mutations, little is known about the molecular mechanism of malignant transformation. We have performed whole-exome sequencing together with CGH+SNP array analysis in 33 flow-cytometry separated abnormal plasma cell samples from MGUS patients to describe somatic gene mutations and chromosome changes at the genome-wide level. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array; Genome variation profiling by SNP array
Platform:
GPL11358
33 Samples
Download data: TXT
Series
Accession:
GSE77979
ID:
200077979
18.

Integrative analysis of DNA copy number, DNA methylation and gene expression in multiple myeloma reveals alterations related to relapse

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array; Methylation profiling by genome tiling array; Expression profiling by array
Platforms:
GPL6244 GPL17148 GPL18637
112 Samples
Download data: CEL, CYCHP, XYS
Series
Accession:
GSE77540
ID:
200077540
19.

Integrative analysis of DNA copy number, DNA methylation and gene expression in multiple myeloma reveals alterations related to relapse [gene expression]

(Submitter supplied) Multiple myeloma (MM) remains incurable despite the introduction of novel agents and a relapsing course is observed in the majority of patients. Although the development of genomic technologies has greatly improved our understanding of MM pathogenesis, the mechanisms underlying relapse have been less investigated. In this study, an integrative analysis of DNA copy number, DNA methylation and gene expression was conducted in matched diagnosis and relapse samples from 17 MM patients. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
34 Samples
Download data: CEL
Series
Accession:
GSE77539
ID:
200077539
20.

Integrative analysis of DNA copy number, DNA methylation and gene expression in multiple myeloma reveals alterations related to relapse [DNA methylation]

(Submitter supplied) Multiple myeloma (MM) remains incurable despite the introduction of novel agents and a relapsing course is observed in the majority of patients. Although the development of genomic technologies has greatly improved our understanding of MM pathogenesis, the mechanisms underlying relapse have been less investigated. In this study, an integrative analysis of DNA copy number, DNA methylation and gene expression was conducted in matched diagnosis and relapse samples from 17 MM patients. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL17148
40 Samples
Download data: XYS
Series
Accession:
GSE77537
ID:
200077537
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