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| Status |
Public on May 04, 2024 |
| Title |
THP1_DMSO_48h_rep3 |
| Sample type |
SRA |
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| Source name |
THP1 human AML cells
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| Organism |
Homo sapiens |
| Characteristics |
treatment: DMSO 0.05percent
time point: 48h
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| Growth protocol |
Cells were grown in RPMI (Corning, 15-040-CV) with 10% dialyzed fetal bovine serum (Sigma, F0392), 4mM glutamine, and 1% penicillin/streptomycin (Corning, 45000-652).
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| Extracted molecule |
total RNA |
| Extraction protocol |
1 million live cells were sorted using a BD FACSAria and placed on ice. Immediately following the sort, cells were centrifuged, pelleted, and flash frozen in liquid nitrogen and placed at -80C. Pellets were processed in groups of 24 using the Zymo RNA Miniprep Kit and quantified using the Invitrogen Quant-it RNA kit. RNA was then diluted to a concentration of 2 ng/ul and 5ul of each sample was transferred to a 96 well plate.
Poly-A enrichment and cDNA synthesis were performed in parallel as described in Soumilion et al. 2014, followed by library preparation using the Nextera XT kit and paired-end sequencing on an Illumina NextSeq 500.
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| Library strategy |
RNA-Seq |
| Library source |
transcriptomic |
| Library selection |
cDNA |
| Instrument model |
Illumina NextSeq 500 |
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| Description |
RNAseq
thp1_thp1_dmso_005pct_48_3
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| Data processing |
Mouse and human data were mapped to mm10 and hg38 genomes, respectively, using STAR v2.7.8a and default parameters.
Reads that mapped to transcripts were counted using featureCounts v2.0.1 (with parameters -M -O --fraction --primary).
Genome_build: mm10
Genome_build: hg38
Supplementary_files_format_and_content: A tab-delimited file containing raw counts generated from featureCounts.
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| Submission date |
Apr 19, 2021 |
| Last update date |
May 04, 2024 |
| Contact name |
Brian Do |
| E-mail(s) |
bdo311@gmail.com
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| Organization name |
MIT
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| Department |
Biology
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| Lab |
Vander Heiden
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| Street address |
500 Main St
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| City |
Cambridge |
| State/province |
MA |
| ZIP/Postal code |
02139 |
| Country |
USA |
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| Platform ID |
GPL18573 |
| Series (2) |
| GSE172333 |
A myeloid maturation program initiated by nucleotide depletion during S phase [RNA-Seq] |
| GSE172335 |
Nucleotide depletion promotes cell fate transitions by inducing DNA replication stress |
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| Relations |
| BioSample |
SAMN18796500 |
| SRA |
SRX10635737 |
| Supplementary data files not provided |
SRA Run Selector |
| Raw data are available in SRA |
| Processed data are available on Series record |
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