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Sample GSM7873336 Query DataSets for GSM7873336
Status Public on Jan 03, 2024
Title Healthy [A4398_103]
Sample type RNA
 
Source name whole blood
Organism Homo sapiens
Characteristics tissue: whole blood
gender / sex: Male
age in days: 56
age group: Below_three_months
visit: Healthy
disease classification at rsv visit based on resvinet score: 1 - Healthy controls
Extracted molecule total RNA
Extraction protocol The whole blood samples were collected in Paxgene tubes (PAXgene® Blood RNA Tube, BD) and stored at –80 °C until the processing. The RNA was extracted using QIAsymphony PAXgene Blood RNA Kit (QIAGEN) according to the manufacturer’s instructions. After the quality control, the RNA was further processed for Clariom™ GOScreen microarray (Thermo Fisher).
Label biotin
Label protocol First strand cDNA was synthesized with a combination of a Poly-dT and random primers containing a 5′-adaptor sequence. A 3’-adaptor was added to the single stranded cDNA followed by low-cycle PCR amplification. The cDNA was used as a template for in vitro transcription (IVT) that produces amplified amounts of antisense mRNA, (cRNA). The cRNA was then used as input for a second round of cDNA synthesis, producing double stranded cDNA.
 
Hybridization protocol After fragmentation, denaturation and end-labeling the targets are hybridized on the single GO Screen plate, according to manufacturer’s instructions (Thermo Fisher; GeneChip Pico Reagent Kit).
Scan protocol Single sample cartridge arrays were stained on a GeneChip Fluidics Station 450 and scanned on a GeneChip scanner 3000 7G while array plates were stained and imaged on the GeneTitan Multi-Channel Instrument.
Description Gene expression data of infants from RESCEU case-control cohort
Data processing Microarray data were preprocessed using R, Bioconductor package 40,41. Robust Multi-Array Average (RMA) function was used to normalize the raw data 42. Outliers were removed from the downstream data analysis based on visual guidance on principal component (PC) spectral map and sample clustering (Pearson correlation with complete linkage).
The clinical data necessary for batch correction (site of sample collection) is accessible by request only from the submitting party.
 
Submission date Oct 31, 2023
Last update date Jan 03, 2024
Contact name Deniz Oner
E-mail(s) deniz.oner@kuleuven.be
Organization name KU Leuven
Street address Gaston Geenslaan
City Leuven
ZIP/Postal code 3001
Country Belgium
 
Platform ID GPL31262
Series (1)
GSE246622 Single-cell immune profiling reveals markers of emergency myelopoiesis that distinguish severe from mild respiratory syncytial virus (RSV) disease in infants

Data table header descriptions
ID_REF
VALUE batch corrected

Data table
ID_REF VALUE
AFFX-BkGr-GC03_st 2.655456359
AFFX-BkGr-GC04_st 2.585510373
AFFX-BkGr-GC05_st 2.585701299
AFFX-BkGr-GC06_st 2.546931452
AFFX-BkGr-GC07_st 2.590531462
AFFX-BkGr-GC08_st 2.641046959
AFFX-BkGr-GC09_st 2.673285343
AFFX-BkGr-GC10_st 2.601760795
AFFX-BkGr-GC11_st 2.629755249
AFFX-BkGr-GC12_st 2.794981951
AFFX-BkGr-GC13_st 2.775680064
AFFX-BkGr-GC14_st 2.875965749
AFFX-BkGr-GC15_st 2.985810874
AFFX-BkGr-GC16_st 3.291373308
AFFX-BkGr-GC17_st 4.001353723
AFFX-BkGr-GC18_st 4.193888905
AFFX-BkGr-GC19_st 4.307810929
AFFX-BkGr-GC20_st 5.316967429
AFFX-BkGr-GC21_st 5.392913965
AFFX-BkGr-GC22_st 6.721604721

Total number of rows: 22593

Table truncated, full table size 673 Kbytes.




Supplementary file Size Download File type/resource
GSM7873336_A4398_103.CEL.gz 412.9 Kb (ftp)(http) CEL

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