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Sample GSM2183724 Query DataSets for GSM2183724
Status Public on Feb 23, 2017
Title mv411_dTAG13_24h_r3
Sample type SRA
 
Source name MLL-AF4 rearranged acute myeloid leukemia
Organism Homo sapiens
Characteristics cell line: MV4;11 (Cas9; ENL-FKBP(F36V); ENL-/-)
bar code: ACAGTG
Treatment protocol Cell were treated with 500 nM dTAG-13 (0.1% DMSO final concentration) for 8, 24, or 96 hours; 500 nM EPZ-5676 (0.1% DMSO final concentration) for 96 hours; or DMSO (0.1%) for 24 or 96 hours
Growth protocol MV4;11 (Cas9; ENL-FKBP(F36V); ENL -/-) cells (MV4;11 parent cell line obtained from the laboratory of Prof. Scott A. Armstrong) were cultured in RPMI supplemented with 10% FBS, penecillin, and streptomycin.
Extracted molecule polyA RNA
Extraction protocol Prior to RNA isolation, cell were counted and total RNA isolation was performed using the miRvana miRNA total RNA isolation kit (ThermoFisher Scientific, AM1560) according to manufacturers instructions. Following isolation, RNA was digested with DNase (Ambion). During isolation, external RNA spike-ins (ERCC, Ambion) were added at the time of cell lysis.
Total RNA was subject to polyA selection and adapter ligation in preparation for next-generation sequencing (Illumina stranded mRNA library prep)
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NextSeq 500
 
Description RNA-seq after 24 hr dTAG-13 (500 nM) treatment
Data processing alignment: HiSat using default settings
expression levels: Gene-level expression measurements for RefSeq genes were reported in fragments per kilobase per million reads (FPKM) by Cufflinks 2.0.0 (http://cufflinks.cbcb.umd.edu/) (Trapnell et al., 2010). Cufflinks assembles transcripts, estimates their abundance, and tests for differential expression and regulation in RNA-Seq samples. FPKM values were ERCC normalized. See methods for further details
Genome_build: hg19
Supplementary_files_format_and_content: ENL_all_fpkm_exprs_norm.txt: Tab-delimited text file matix containing ERCC cell count normalized FPKM values for each transcript
 
Submission date Jun 01, 2016
Last update date May 15, 2019
Contact name James Bradner
E-mail(s) bradner_computation@dfci.harvard.edu
Organization name Dana-Farber Cancer Institute
Department Medical Oncology
Lab Bradner Lab
Street address 450 Brookline
City Boston
State/province MA
ZIP/Postal code 02215
Country USA
 
Platform ID GPL18573
Series (2)
GSE82117 Transcription control by the ENL YEATS domain in acute leukemia [RNA-seq]
GSE82118 Transcription control by the ENL YEATS domain in acute leukemia
Relations
BioSample SAMN05194767
SRA SRX1813457

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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