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Sample GSM3374556 Query DataSets for GSM3374556
Status Public on Nov 01, 2018
Title WT_1
Sample type SRA
 
Source name pro-B cell
Organism Mus musculus
Characteristics cell type: pro-B cell
strain: C57BL/6
age: 6-7 weeks
hsc markers: B220+, CD19+, IgM-, IgD-, ckit+, CD25-
genotype/variation: wild type
Extracted molecule polyA RNA
Extraction protocol Pro-B cells were sorted directly into RLT (Qiagen) lysis buffer and RNA extracted with micro Rneasy columns. RNA quality and quantity was determined by a Bioanalyzer and normalized for library construction.
Libraries were prepared with the SMARTER method for low-input RNA using standard Illumni procedures.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Data processing Sequenced reads were trimmed for adaptor sequence and mapped to the mm9 genome with bowtie.
FPKM values and differential expression was determined using cuffdiff.
Genome_build: mm9
 
Submission date Sep 04, 2018
Last update date Nov 01, 2018
Contact name David Cantor
E-mail(s) David.Cantor@med.nyu.edu
Organization name NYU School of Medicine
Lab Gregory David Lab
Street address 550 First Avenue
City New York
State/province New York
ZIP/Postal code 10016
Country USA
 
Platform ID GPL17021
Series (1)
GSE119422 Identification of Bmi1 regulated genes in pro-B cells
Relations
BioSample SAMN09951205
SRA SRX4637665

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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