|
| Status |
Public on May 10, 2018 |
| Title |
R290-96 |
| Sample type |
SRA |
| |
|
| Source name |
NEPRC
|
| Organism |
Macaca mulatta |
| Characteristics |
gender: Male
cell type: Lymphoblastoid Cell
cell line: R290-96
enrichment type: ribosome protected fragments
|
| Growth protocol |
Cells were cultured at 37 degree Celsius and 5% CO2 in RPMI 1640 (supplemented with 2mM L-glutamine and 15% fetal bovine serum)
|
| Extracted molecule |
cytoplasmic RNA |
| Extraction protocol |
Ribosome footprint profiling experiments were performed using ARTseqTM Ribosome Profiling kit for mammalian cells (RPHMR12126) following vendor’s instructions. Cell lysates were prepared from flash frozen pellets of 30 to 50 million live cells by repeat pipetting in 1 ml cold lysis buffer. Sephacryl S400 spin column (GE; 27-5140-01) was used for monosome isolation. For rRNA depletion, Ribo-Zero Magnetic Kit (Epicentre; MRZH11124) was used.
Ribosome footprint cDNA libraries were PCR amplified (12 to 15 thermo-cycles) and barcoded using ScriptMiner Index PCR Primers (Epicentre; SMIP2124). Indexed libraries were pooled to sequence on an Illumina HiSeq 2500.
|
| |
|
| Library strategy |
OTHER |
| Library source |
transcriptomic |
| Library selection |
other |
| Instrument model |
Illumina HiSeq 2500 |
| |
|
| Description |
R290-96
|
| Data processing |
Sequencing image analysis and basecalling were performed using CASAVA version 1.7.0
Raw data provided are fastq files after the following processing. FASTX-Toolkit were used to clip the adaptor sequence and trim the 5' most base for each read. Reads that are shorter than 22-nt or that are mapped to rRNA, tRNA, snoRNA using bowtie were removed from the file.
Processed reads are then map to human genome (hg19) or chimpanzee genome (PanTro3) or rhesus macaque gemome (rheMac2) respectively using BWA. Uniquely mapped reads are used to intersect with orthologous gene annotations using BEDTools to get read count per gene for each individual.
Genome_build: hg19 or PanTro3 or rheMac2
Supplementary_files_format_and_content: Processed data file contains read count per orthologous gene for each individual. It is organized with one individual per column and one gene per row. The first two columns are ENSG ID and gene length.
|
| |
|
| Submission date |
Aug 06, 2015 |
| Last update date |
May 15, 2019 |
| Contact name |
Sidney Wang |
| E-mail(s) |
siddisis@gmail.com
|
| Organization name |
University of Chicago
|
| Department |
Human Genetics
|
| Street address |
920 E. 58th Street, CLSC 317
|
| City |
Chicago |
| State/province |
IL |
| ZIP/Postal code |
60637 |
| Country |
USA |
| |
|
| Platform ID |
GPL19129 |
| Series (1) |
| GSE71808 |
Post-translational buffering leads to convergent protein expression levels between primates |
|
| Relations |
| SRA |
SRX1135829 |
| BioSample |
SAMN03979384 |
