|
Status |
Public on May 25, 2018 |
Title |
ASXL1-MT rep3 |
Sample type |
SRA |
|
|
Source name |
Bone marrow progenitor cells
|
Organism |
Mus musculus |
Characteristics |
strain: C57BL/6 tissue: Bone marrow progenitor cells age: 8- to 12-week-old transduced genes: ASXL1-MT
|
Growth protocol |
Cells were cultured in M3234 methylcellulose containing 20 ng/ml SCF, 10 ng/ml IL-3 and 10 ng/ml IL-6 according to manufacturer’s instructions.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was prepared using RNeasy mini kit (QIAGEN). RNA libraries were prepared for sequencing using NEBNext Ultra Directional RNA Library Prep Kit for Illumina according to the manufacturer's protocol.
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2500 |
|
|
Data processing |
Illumina Casava1.8.2 software used for basecalling. Sequenced reads were mapped to the mouse genome (mm10) using TopHat v2.0.9, with default parameters. Normalized read counts were calculated using HTSeq 0.6.1p1 (-s reverse -m intersection-strict) and DESeq22 1.6.3 with VST normalization. Genome_build: mm10 Supplementary_files_format_and_content: Tab-delimited text files include FPKM values for each Sample.
|
|
|
Submission date |
May 24, 2018 |
Last update date |
May 25, 2018 |
Contact name |
Shuhei Asada |
Organization name |
Institute of Medical Science, The University of Tokyo
|
Department |
Cellular Therapy
|
Lab |
Kitamura Lab
|
Street address |
4-6-1 Shirokanedai, Minato-ku
|
City |
Tokyo |
ZIP/Postal code |
1088639 |
Country |
Japan |
|
|
Platform ID |
GPL17021 |
Series (1) |
GSE114861 |
The effects of mutant ASXL1 and BAP1 expression on hematopoietic cells |
|
Relations |
BioSample |
SAMN09246027 |
SRA |
SRX4119898 |