|
Status |
Public on Jan 11, 2023 |
Title |
Patient 1 |
Sample type |
SRA |
|
|
Source name |
peripheral blood
|
Organism |
Homo sapiens |
Characteristics |
tissue: peripheral blood cell type: CD4 treatment: HAART
|
Treatment protocol |
samples were not treated correspond to primary cells isolated ex vivo
|
Growth protocol |
n/a
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was obtained using the Qiagen RNeasy Micro Kit RNA-Seq libraries from mDC were generated as previously described by Trombetta JJ et al Current Protocols in molecular biology, 2014
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NextSeq 500 |
|
|
Description |
S01
|
Data processing |
FASTQ files were obtained by Illumina bcl2fastq2. STAR and RSEM were used to align to GRCh38 and to calculate the raw counts for genes, respectively. Assembly: GRCh38 Supplementary files format and content: raw counts and TPM in csv
|
|
|
Submission date |
Nov 22, 2022 |
Last update date |
Jan 11, 2023 |
Contact name |
Ce Gao |
E-mail(s) |
[email protected]
|
Organization name |
Ragon Institute of MGH, MIT and Harvard
|
Lab |
Yu/Lichterfeld Labs
|
Street address |
400 Technology Square
|
City |
Cambridge |
State/province |
MA |
ZIP/Postal code |
02139 |
Country |
USA |
|
|
Platform ID |
GPL18573 |
Series (1) |
GSE218587 |
Cooperation between cGAS and RIG-I sensing pathways enables improved innate recognition of HIV-1 by myeloid dendritic cells in elite controllers |
|
Relations |
BioSample |
SAMN31840957 |
SRA |
SRX18353208 |