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Status |
Public on May 14, 2023 |
Title |
63test-2 |
Sample type |
SRA |
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Source name |
MG63
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Organism |
Homo sapiens |
Characteristics |
cell line: MG63 cell type: non-metastatic osteosarcoma cell line genotype: IDO OE
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Growth protocol |
MG63 and 143B cells were cultured in DMEM (Gibco, USA) supplement with 10% (vol/vol) fetal bovine serum (FBS, Gibco, USA), 100 μg/mL penicillin and streptomycin (Gibco, USA) at 37°C. The hFOB1.19 cells were cultured in DMEM/F12 (Gibco, USA) supplement with 10% (vol/vol) FBS (Gibco, USA), 1% (vol/vol) nonessential amino acid solution (Gibco, USA), 0.3 mg/mL G418 and 100 μg/mL penicillin and streptomycin (Gibco, USA) at 33.5°C. Cells were cultured in an atmosphere of 5% CO2 and 90% relative humidity.
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Extracted molecule |
total RNA |
Extraction protocol |
Exosomes were isolated from cell culture supernatant with the exoEasy Maxi Kit (Qiagen, No. 76046, USA) according to the manufacturer’s instructions. Total RNA was isolated from exosomes following the protocol of the exoRNeasy SerumKit (Qiagen, No. 77064, USA). Extracted RNA was used to prepare the miRNA sequencing library with QIAseq miRNA Library Kit (Qiagen, No. 331505, USA).
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Library strategy |
miRNA-Seq |
Library source |
transcriptomic |
Library selection |
size fractionation |
Instrument model |
Illumina NovaSeq 6000 |
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Data processing |
Raw data were generated after sequencing, image analysis, base calling, and quality filtering on the Illumina sequencer. Firstly, Q30 was used to perform quality control. The adaptor sequences were trimmed and the adaptor-trimmed reads (>= 15nt) were left by cutadapt software (v1.9.3). Then, trimmed reads from all samples were pooled, and miRDeep2 software (v2.0.0.5) was used to predict novel miRNAs. The trimmed reads were aligned to the merged pre-miRNA databases (known pre-miRNA from miRBase v22 plus the newly predicted pre-miRNAs) using Novoalign software (v3.02.12) with at most one mismatch. The numbers of mature miRNA mapped tags were defined as the raw expression levels of that miRNA. The read counts were normalized by the edgeR approach. Supplementary files format and content: The raw and normalized tag counts of the mature miRNA.
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Submission date |
May 12, 2023 |
Last update date |
May 14, 2023 |
Contact name |
Dan Yang |
E-mail(s) |
yangdanmuzi@126.com
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Organization name |
Shanghai Children's Hospital
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Street address |
355 Luding Road, Putuo District
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City |
Shanghai |
ZIP/Postal code |
200062 |
Country |
China |
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Platform ID |
GPL24676 |
Series (1) |
GSE232452 |
IDO1 overexpression significantly affects exosomal miRNA subsets derived from osteosarcoma and ordinary osteoblasts |
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Relations |
BioSample |
SAMN35065468 |
SRA |
SRX20313900 |
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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