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Status |
Public on Feb 14, 2018 |
Title |
Profiling of expression data in melanoma cells following DOT1L shRNA knockdown |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
|
Summary |
DOT1L-dependent H3K79 methylation is associated with telomere silencing, meiotic checkpoint control, DNA repair, modulation of constitutive heterochromatin, and transcriptional activation.
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Overall design |
We used microarrays to detail the global program of gene expression in C021 melanoma cells following treatment with shRNA against DOT1L or scrambled control.
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Contributor(s) |
Zhu B, Cui R |
Citation(s) |
29343685 |
Submission date |
Aug 24, 2017 |
Last update date |
Jul 25, 2021 |
Contact name |
Boston University Microarray and Sequencing Resource |
E-mail(s) |
msrdata@bu.edu
|
Organization name |
Boston University
|
Department |
Microarray and Sequencing Resource
|
Street address |
72 East Concord Street, E631
|
City |
Boston |
State/province |
MA |
ZIP/Postal code |
02118 |
Country |
USA |
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Platforms (1) |
GPL17930 |
[HuGene-2_0-st] Affymetrix Human Gene 2.0 ST Array [HuGene20stv1_Hs_ENTREZG_17.0.0] |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE103081 |
Profiling of expression data in melanoma cells with mutant DOT1L, DOT1L inhibitor or shRNA knockdown |
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Relations |
BioProject |
PRJNA400279 |