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Status |
Public on Nov 19, 2022 |
Title |
2B-NNK cells,NNK treatment 2 |
Sample type |
SRA |
|
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Source name |
lung
|
Organism |
Homo sapiens |
Characteristics |
tissue: lung cell line: BEAS-2B cell type: epithelial cell genotype: WT treatment: NNK treatment
|
Treatment protocol |
Cells were seeded in 6-well plates containing 100 mg/L NNK and cultured for 24 h every 4 d. Finally, the total amount of NNK processed was 1mg.
|
Growth protocol |
BEAS-2B and 2B-NNK cells were maintained in BEBM supplemented with 10% fetal bovine serum (FBS) and antibiotics in humidified atmosphere with 5% CO2 at 37C
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was harvested using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) . 1.3 ug of total RNA was used for the construction of sequencing libraries. RNA libraries for RNA-seq were prepared using KAPA Stranded RNA-Seq Library Prep Kit(Illumina) following manufacturer's protocols.
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
|
|
Data processing |
hisat2 v 2.1.0 Sequence reads were trimmed for adaptor sequence/low-quality sequence using Cutadapt v 1.17 (parameter- Mapped: 0.85) Trimmed sequence reads were mapped to GRCh37 using hisat2 Read count extractionwas performed using hisat2. Read count normalization was performed using R package "Ballgown". Assembly: GRCh37 Supplementary files format and content: matrix table files include FPKM values for each Sample
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Submission date |
Nov 15, 2022 |
Last update date |
Nov 19, 2022 |
Contact name |
qiaoyuan yang |
E-mail(s) |
yqy1208@126.com
|
Phone |
+86 13697414042
|
Organization name |
Guangzhou Medical University
|
Street address |
Xinzao Town, Panyu District
|
City |
Guangzhou |
ZIP/Postal code |
511436 |
Country |
China |
|
|
Platform ID |
GPL24676 |
Series (1) |
GSE217991 |
Chimeric RNA RRM2-C2orf48 plays an oncogenic role in the development of NNK-induced lung cancer |
|
Relations |
BioSample |
SAMN31727459 |
SRA |
SRX18271971 |