Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

ArrayCGH on a cohort of pediatric T-ALLs to investigate the mechanism of primary chemotherapy resistance

ABSTRACT: ArrayCGH was performed on a cohort of 36 specimens collected from children with newly diagnosed T-ALL treated on contemporary clinical trials. The data was used to investigate mechanisms of primary chemotherapy resistance in T-ALL.

ORGANISM(S): Homo sapiens

PROVIDER: GSE96624 | GEO | 2018/10/16

REPOSITORIES: GEO

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
		Other

Items per page:

1 - 1 of 1

Similar Datasets

ArrayCGH on a cohort of pediatric T-ALL cases characterized by TCRAD-MYC translocation

Project description:ArrayCGH was performed on a cohort of 25 specimens collected from children with newly diagnosed T-ALL characterized by TCRAD-MYC translocation ArrayCGH analyses were perfomed to study genomic aberrations occurring in the rare subgroup of TCRAD-MYC rearranged T-ALL

2018-07-01 | GSE106773 | GEO

Oligonucleotide-based arrayCGH

Project description:Oligonucleotide-based arrayCGH

| PRJNA92921 | ENA

Pituitary Gigantism ArrayCGH

Project description:Pituitary Gigantism ArrayCGH

| PRJNA940053 | ENA

ArrayCGH on a cohort of pediatric T-ALL cases characterized by TCRAD-MYC translocation

Project description:ArrayCGH on a cohort of pediatric T-ALL cases characterized by TCRAD-MYC translocation

| PRJNA417967 | ENA

ArrayCGH of human hepatocellular carcinoma (HCC)

Project description:We used array-based comparative genomic hybridization (arrayCGH) of 76 hepatocellular carcinomas (HCCs) to search for genetically disrupted genes.

2012-01-20 | GSE14322 | GEO

Comprehensive genomic analysis of relapse neuroblastoma [arrayCGH]

Project description:Relapse neuroblastoma were characterized by sequencing, gene expression, arrayCGH and genome-wide methylation. This data set contains the aCGH data.

2015-06-19 | GSE65304 | GEO

ArrayCGH study to investigate duplication of T locus in chordoma

Project description:Duplication of T is a known familial susceptibility determinant for chordoma. TO determine if a similar genetic alteration occurs in the sporadic disease a high-resolution array-CGH (Agilent custom-designed arrayCGH chip) was used to interrogate the chr 6q27 locus for duplication of T. Twenty two samples of chordoma and reference genomic DNA were hybridised to the chip including a positive control from a chordoma cell line.

2012-10-04 | E-MEXP-3753 | biostudies-arrayexpress

ArrayCGH mapping of the recurrent 3q26.3-q27 amplifications in lung Squamous Cell Carcinoma (SCC)

Project description:To prospectively identify new oncogenes implicated in lung Squamous Cell Carcinoma pathogenesis, we investigated chromosome 3 aberrations in advanced tumours using arrayCGH. Chromosome 3 aberrations are indeed among the most frequent alterations in lung SCC and correlate with SCC patient's poor prognosis. We have precisely mapped regions of recurrent losses at 3p and gains at 3q25-qter in a series of lung SCC (GSE14859) amd moreover uncover 3q26.3-q27 high level amplifications in 20% of tumours. These amplicons were precisely mapped in these tumors using arraCGH with a 3q26.3 dedicated tiling array. Keywords : ArrayCGH, lung Squamous Cell Carcinoma, 3q26.3, SOX2 Keywords: ArrayCGH

2010-02-10 | GSE15079 | GEO

ArrayCGH mapping of chromosome 3 aberrations in lung Squamous Cell Carcinoma (SCC)

Project description:To prospectively identify new oncogenes implicated in lung Squamous Cell Carcinoma pathogenesis, we investigated chromosome 3 aberrations in advanced tumours using arrayCGH. These aberrations are indeed among the most frequent aberrations in lung SCC and correlate with SCC patient's poor prognosis. We precisely map regions of recurrent losses at 3p and gains at 3q25-qter in a series of lung SCC. We moreover uncover 3q26.3-q27 high level amplifications in 20% of tumours. Keywords: ArrayCGH, Lung Squamous Cell Carcinoma, 3q26.3, SOX2

2010-02-10 | GSE14859 | GEO

ArrayCGH experiments involving patients with T-ALL

Project description:We consider a data set consisting out of 27 arrayCGH dye-swap experiments (54 arrays) of individuals with T-ALL versus normal individuals. Aim was to detect novel unbalanced genomic rearrangements in T-ALL. Analysis of the patients was done using an array with genomic BAC and PAC probes with an overall resolution of 1Mb over the entire genome and with additional probes around known and candidate oncogenes. Keywords: comparative genomic hybridization, genotype

2007-04-15 | GSE7239 | GEO

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data