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Status |
Public on Oct 06, 2023 |
Title |
siNC-2 |
Sample type |
SRA |
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Source name |
human macrophages
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Organism |
Homo sapiens |
Characteristics |
tissue: peripheral blood cell type: THP1 monocyte cell line -derived macrophages treatment: THP1-derived macrophages were transfected with control siRNA for 48 h.
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Treatment protocol |
THP1-derived macrophages were transfected with METTL3 siRNA pools or control siRNA for 48 h. Then, macrophages were stimulated with IL-4 (20 ng/ml) for 24 h.
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Growth protocol |
Human THP1 cell lines (purchased from the American Type Culture Collection (ATCC), USA) were maintained in RPMI-1640 medium, 10% heat-inactivated FBS. To generate macrophage-like cells, THP-1 cell were seeded along with 200 nM PMA for 48 h. Cells were incubated at 37 °C with 5% CO2.
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using RNeasy Micro Kit (Cat#74004, Qiagen)following the manufacturer’s instructions and checked for a RIN number to inspect RNA integrity by an Agilent Bioanalyzer 2100 (Agilent technologies, Santa Clara, CA, US).Qualified total RNA was further purified by RNAClean XP Kit (Cat A63987, Beckman Coulter,Inc.Kraemer Boulevard Brea, CA,USA)and RNase-Free DNase Set (Cat#79254, QIAGEN, GmBH, Germany) Paired-end libraries were synthesized by using the TruSeq™ RNA Sample Preparation Kit (Illumina, USA) following TruSeq™ RNA Sample Preparation Guide
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
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Data processing |
Illumina Casava1.7 software used for basecalling. Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to mm8 whole genome using bowtie v0.12.2 with parameters -q -p 4 -e 100 -y -a -m 10 --best --strata Differentially expressed genes were identified using Cuffdiff. The p-value significance threshold in multiple tests was set by the false discovery rate (FDR). The fold-changes were also estimated according to the FPKM in each sample. Genome_build: GRCh38.91 Supplementary_files_format_and_content: tab-delimited text files include FPKM values for each Sample .
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Submission date |
Dec 23, 2021 |
Last update date |
Oct 06, 2023 |
Contact name |
Xiao Han |
E-mail(s) |
sqhx12@126.com
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Phone |
02164932897
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Organization name |
Children’s Hospital of Fudan University
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Street address |
399 Wanyuan Rd, Minhang, Shanghai, China
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City |
Shanghai |
State/province |
Select state... |
ZIP/Postal code |
201102 |
Country |
China |
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Platform ID |
GPL24676 |
Series (1) |
GSE192533 |
Differenatiation of mRNA expression in METTL3-depleted macrophages |
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Relations |
BioSample |
SAMN24365690 |
SRA |
SRX13496396 |
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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