NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM7059265 Query DataSets for GSM7059265
Status Public on Jan 16, 2024
Title Eosinophils__P51
Sample type SRA
 
Source name peripheral blood cells
Organism Homo sapiens
Characteristics tissue: peripheral blood cells
cell type: Eosinophils
Extracted molecule total RNA
Extraction protocol The fractional blood derivatives as well as the whole blood samples were directly lysed in Qiazol. For RNA isolation the miRNeasy Serum/Plasma mini kit was combined with minElute columns.
Dual indexed sRNA libraries with unique molecular identifiers (UMIs) adaptors were generated using the QIAseq miRNA Library Kit.
 
Library strategy miRNA-Seq
Library source transcriptomic
Library selection size fractionation
Instrument model NextSeq 2000
 
Data processing Raw sequence reads were adapter trimmed and depleted of PCR duplicates based on the UMIs.
Only sequences that had at least one read in at least three samples per blood component type and that were longer than 17 nucleotides were kept.
For 25 cellular fractions (4.6% of derivatives, 25/539) the purification process did not meet the prespecified quality standard (purity > 70% as determined by flow cytometry). These samples were excluded from further analyses. See 'quality filter for processed data'
As additional quality control, the normalized data of the blood component samples was converted to a two-dimensional T-distributed Stochastic Neighbor Embedding (t-SNE) space. When plotting the two embedding vectors against each other, four samples did not cluster with the samples of the same blood component type (0.8% of derivatives, 4/514) and were excluded from further analysis. See 'quality filter for processed data'
The pre-processed sRNA sequences were annotated using the annotation pipelines unitas and SPORTS. In case of multi-assignments, the annotation was prioritized in the following manner: miRNA > tRNA > rRNA > YRNA > snoRNA > lncRNA > snRNA > piRNA.
Assembly: hg38
Supplementary files format and content: csv files including log2-transformed RPM values per small RNA name for all blood component samples (1 file) and for all whole blood samples (1 file)
 
Submission date Feb 22, 2023
Last update date Jan 16, 2024
Contact name Bruno Steinkraus
E-mail(s) publication@hb-dx.com
Phone 062219143350
Organization name HUMMINGBIRD DIAGNOSTICS GMBH
Street address Im Neuenheimer Feld 583
City Heidelberg
State/province Baden-Württemberg
ZIP/Postal code 69120
Country Germany
 
Platform ID GPL30173
Series (1)
GSE225872 miR-Blood - a small RNA sequencing atlas of purified human blood components
Relations
BioSample SAMN33418720
SRA SRX19476438

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap