|
Status |
Public on Oct 20, 2016 |
Title |
risk (CC) (sample 57) |
Sample type |
SRA |
|
|
Source name |
PBMCs
|
Organism |
Homo sapiens |
Characteristics |
cell type: EBV (Epstein Barr Virus)-transformed B lymphocyte cells genotype: (CC)
|
Growth protocol |
Cells were maintained in RPMI and the media was changed every third day.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA from EBV (Epstein Barr Virus)-transformed B lymphocyte cells, from 3 carriers of the risk (CC) allele and 3 non-carriers of the (GG) reference allele, was isolated using the Qiagen RNeasy-Midi kit (Cat#75142). Illumina TruSeq RNA Sample Prep Kit (Cat#FC-122-1001) was used with 1 ug of total RNA for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols.
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina Genome Analyzer IIx |
|
|
Data processing |
Perkin Elmer's Genesifter Analysis Edition Software Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to Human Build 37.2 using BWA. Raw read count was normalized by total mapped million reads (RPM). Benjamini-Hochberg correction Genome_build: 37.2 Supplementary_files_format_and_content: Excel files include raw and RPM values for combined triplicate samples.
|
|
|
Submission date |
Oct 12, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Annabelle Rodriguez |
E-mail(s) |
rodriguezoquendo@uchc.edu
|
Phone |
(860) 679-2463
|
Organization name |
UCONN Health
|
Department |
Center for Vascular Biology
|
Lab |
Rodriguez
|
Street address |
263 Famington Ave, MC-3501
|
City |
Farmington |
State/province |
CT |
ZIP/Postal code |
06030-3501 |
Country |
USA |
|
|
Platform ID |
GPL10999 |
Series (1) |
GSE87891 |
Lymphocyte activation gene3 and coronary artery disease. |
|
Relations |
BioSample |
SAMN05901242 |
SRA |
SRX2241075 |