|
Status |
Public on May 01, 2016 |
Title |
MP 2 |
Sample type |
SRA |
|
|
Source name |
bone marrow progenitor
|
Organism |
Mus musculus |
Characteristics |
sample type: Lin-Sca-1-c-Kit+ mouse bone marrow cells strain: FVB N/J
|
Growth protocol |
GFP-labled APL cells were expanded in vivo via transplantation into syngeneic mice.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted with AMBION AM1560 kit. Following "TruSeq RNA Sample Preparation Guide".
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2000 |
|
|
Description |
HPC-2
|
Data processing |
Basecalls performed using CASAVA version 1.8 Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence using FASTX-Toolkit version 0.0.13 and Perl version 5.8.8 mRNA-seq reads were aligned to the mm10 genome assembly using Tophat version 2.0.6 with parameters: -r 100 -I 50000 --max-segment-intron 50000 -a 10 -g 10 Gene abundance measurements were generationed and normalized using Cufflink version 2.0.2.Linux_x86_64 ; The normalized standard were Fragments Per Kilobase of exon per Megabase of library size (FPKM) Differential expression were analysed using DEGseq function package in R program version 2.10.0 Genome_build: UCSC mm10 Supplementary_files_format_and_content: tab-delimited text files include normalized FPKM values and raw fragment counts for each Sample
|
|
|
Submission date |
Apr 26, 2013 |
Last update date |
May 15, 2019 |
Contact name |
Jiang Zhu |
E-mail(s) |
zhujiang@shsmu.edu.cn
|
Organization name |
Shanghai institute of hematology
|
Street address |
197, rui-jin 2nd Road
|
City |
Shanghai |
ZIP/Postal code |
200025 |
Country |
China |
|
|
Platform ID |
GPL13112 |
Series (1) |
GSE46434 |
Expression data from GFP-labeled c-Kit+ mouse APL cells and normal Lin-Sca-1-c-Kit+ mouse bone marrow cells |
|
Relations |
BioSample |
SAMN02058598 |
SRA |
SRX272199 |