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SRX20273496: GSM7312258: P1-SCAF2961_1_Uninfected, HCT116, THP1 and Jurkat T, Uninfected, 10x genomics 3' v3; Homo sapiens; RNA-Seq
2 ILLUMINA (Illumina NovaSeq 6000) runs: 455.8M spots, 53.8G bases, 15.9Gb downloads

External Id: GSM7312258_r1
Submitted by: Cancer Data Science Laboratory, National Cancer Institute, National Institutes of Health
Study: scRNA-seq analysis of colon and esophageal tumors uncovers abundant microbial reads in myeloid cells undergoing proinflammatory transcriptional alterations
show Abstracthide Abstract
We profiled cell lines (HCT116, THP1 and Jurkat T) exposed to heat-killed and live Fusobacterium nucleatum using multiple scRNA-seq technologies Overall design: We profiled cell lines (HCT116, THP1 and Jurkat T) exposed to heat-killed and live Fusobacterium nucleatum using multiple scRNA-seq technologies
Sample: P1-SCAF2961_1_Uninfected, HCT116, THP1 and Jurkat T, Uninfected, 10x genomics 3' v3
SAMN35015926 • SRS17601241 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: GSM7312258
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC SINGLE CELL
Selection: cDNA
Layout: PAIRED
Construction protocol: Single cell suspensions were prepared, and concentration and viability measured on an automated dual-fluorescence cell counter with acridine orange and propidium iodide stain (Luna Fx7, Logos Biosystems). Single cell partitioning and RNA-Seq library preparation was performed using 10X genomics 3' v3.1 chemistry (user guide CG000204) according to vendor recommendations. Sample viability was above 80% for all conditions. 6,000-8,000 cells were targeted to be captured for each sample. Libraries were sequenced on the NovaSeq 6000 with a target depth of 50,000 reads per cell using read parameters recommended by 10x Genomics user guides.
Runs: 2 runs, 455.8M spots, 53.8G bases, 15.9Gb
Run# of Spots# of BasesSizePublished
SRR24488149228,800,50927G7.9Gb2023-05-23
SRR24488150226,975,85426.8G7.9Gb2023-05-23

ID:
27694429

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