|
|
GEO help: Mouse over screen elements for information. |
|
Status |
Public on Jun 30, 2022 |
Title |
AKATA |
Sample type |
SRA |
|
|
Source name |
B cell lymphoma cell
|
Organism |
Homo sapiens |
Characteristics |
cell line: AKATA tissue: B cell lymphoma cell type: EBV positive B cell lymphoma cell line
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA from TW03-EV and TW03-Gal-9 cells were isolated using TRIzol reagent, and dissolved in RNase-free water. RNA libraries were prepared for sequencing using standard Illumina protocols
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 3000 |
|
|
Data processing |
Illumina Bcl2FastQ software used for basecalling. Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to hg19 whole genome using TopHat v2.0.13 with parameters -p 8 --read-mismatches 2 --read-gap-length 2 --read-edit-dist 2 -G hg19 Reads Per Kilobase of exon per Megabase of library size (RPKM) were calculated using a protocol from Chepelev et al., Nucleic Acids Research, 2009. In short, exons from all isoforms of a gene were merged to create one meta-transcript. The number of reads falling in the exons of this meta-transcript were counted and normalized by the size of the meta-transcript and by the size of the library. Genome_build: hg19 Supplementary_files_format_and_content: tab-delimited text files include Counts and RPKMs for each Sample
|
|
|
Submission date |
Dec 02, 2020 |
Last update date |
Jun 30, 2022 |
Contact name |
Jingxiao Xu |
E-mail(s) |
xujx1@sysucc.org.cn
|
Phone |
17825845830
|
Organization name |
Sun Yet san university
|
Street address |
Dongfengdong Road 651
|
City |
Guangzhou |
State/province |
Guangdong Province |
ZIP/Postal code |
510000 |
Country |
China |
|
|
Platform ID |
GPL21290 |
Series (1) |
GSE162516 |
Critical role of galectin-9 in EBV-driven transformation of human B-lymphocytes |
|
Relations |
BioSample |
SAMN16981102 |
SRA |
SRX9620198 |
Supplementary file |
Size |
Download |
File type/resource |
GSM4953587_AKATA_positive_analysed.txt.gz |
1.3 Mb |
(ftp)(http) |
TXT |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
|
|
|
|
|