GSM3660619[Accession] - GEO DataSets

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Items: 3

Select item 2001280311.

Integrated genomic analysis of chromosomal alterations and mutations in B-cell acute lymphoblastic leukemia reveals distinct genetic profiles at relapse

(Submitter supplied) Background: The clonal basis of relapse in acute lymphoblastic leukemia (ALL) is complex and not fully understood. Methods: Next-generation sequencing (NGS), array comparative genomic hybridization (aCGH), and multiplex-ligation-dependent probe amplification (MLPA) were carried out in matched diagnosis-relapse samples from 13 B-cell precursor acute lymphoblastic leukemia (BCP-ALL) patients to identify patterns of genetic evolution that could account for the phenotypic changes associated with disease relapse. more...

Organism:: Homo sapiens

Type:: Genome variation profiling by genome tiling array

Platform:: GPL10197
26 Samples

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Accession:: GSE128031

ID:: 200128031

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Select item 1000101972.

Nimblegen Human 12x135K array [090527_HG18_WG_CGH_v3.1_HX12]

(Submitter supplied) 12x135K Arrays Content sourced from the UCSC hg18 human genome (NCBI build 36, March 2006) designname=090527_HG18_WG_CGH_v3.1_HX12 designid=10032 Protocol: see manufacturer's web site (http://www.nimblegen.com/)