|
Status |
Public on Jul 03, 2024 |
Title |
10220_Pre-Infection_TCRgd |
Sample type |
SRA |
|
|
Source name |
PBMC
|
Organism |
Homo sapiens |
Characteristics |
tissue: PBMC cell line: NA cell type: gamma delta T cells genotype: NA treatment: none
|
Treatment protocol |
Cells were not treated other than staining and sorting
|
Growth protocol |
Cryopreserved PBMC were thawed, stained, and sorted directly without any culture
|
Extracted molecule |
total RNA |
Extraction protocol |
200 cells were directly sorted into 1x lysis buffer supplemented with 6U RNase inhibitor (both Takara Bio). Post sort, sample tubes were vortexed, incubated at RT for 2 minutes, and snap frozen on dry ice prior to storage at -80˚ C. Upon thawing, cDNA synthesis was performed using the SMART-Seq v4 Ultra Low Input RNA Kit (Takara Bio) as per the manufacturer’s instructions. A total of 150-300pg amplified cDNA was used as input for library preparation
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina MiSeq |
|
|
Description |
Broad neutralizer
|
Data processing |
Quality control was performed on raw FASTQ files using FastQC to assess the quality of the sequencing data. Adapters and low-quality bases were trimmed using Trimmomatic. Cleaned reads were aligned to the reference genome using STAR aligner(ver. 2.6.1d) with default parameters. Aligned reads were quantified to gene-level expression using RSEM(ver. 1.3.1). Raw read counts and TPM (Transcripts Per Million) were generated for each sample. Differential expression analysis was carried out using edgeR. Assembly: hg38 Supplementary files format and content: The processed data files are in tab-delimited text format and include gene expression matrices (TPM and raw counts) and differential expression results (gene IDs, log2 fold changes, p-values, and FDR).
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|
|
Submission date |
Jul 03, 2024 |
Last update date |
Jul 04, 2024 |
Contact name |
Dohoon Kim |
E-mail(s) |
dkim@hivresearch.org
|
Organization name |
Henry M Jackson Foundation
|
Street address |
503 BLDG, Walter Reed Army institute of research
|
City |
silver spring |
ZIP/Postal code |
20910 |
Country |
USA |
|
|
Platform ID |
GPL15520 |
Series (1) |
GSE271442 |
CD16 and CD57 Expressing Gamma Delta T Cells in Acute HIV-1 Infection are Associated with the Development of Neutralization Breadth |
|
Relations |
BioSample |
SAMN42305996 |
SRA |
SRX25204473 |