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Sample GSM7498835 Query DataSets for GSM7498835
Status Public on Sep 20, 2023
Title notaddDrug_2, ip
Sample type SRA
 
Source name PANC-1
Organism Homo sapiens
Characteristics cell line: PANC-1
cell type: Human PDAC cell lines
genotype: not Cytochalasin D treatment
treatment: m6A
Treatment protocol Purified RNA was fragmented and incubated with anti-m6A antibody (Synaptic Systems, 202003)-conjugated beads in RIP reaction buffer overnight at 4 °C
After incubation, the bound RNAs were purified via proteinase K treatment, acidic phenol/chloroform extraction and ethanol precipitation
Growth protocol Total RNA from cell lines was isolated by using Trizol reagent (Invitrogen). The RNA samples were quantified by measuring absorbance at 260 nm with a UV spectrophotometer, and only analytes with an RNA integrity number (RIN) ≥ 7.0 were used in further experiments.
Extracted molecule total RNA
Extraction protocol One tenth of the fragmented RNA served as an input control in RNA sequencing.
RNA fragments from the m6A-IP and input samples were used for cDNA library preparation and sequenced on an Illumina HiSeqX Ten PE150 platform.
 
Library strategy OTHER
Library source transcriptomic
Library selection other
Instrument model HiSeq X Ten
 
Description notaddDrug_2, ip
Data processing Clean reads were mapped the hg19 genome using STAR
MACS2 were used to identify peaks
Peaks from each sample were merged to a set of union peaks using BEDTools merge.
Assembly: hg19
Supplementary files format and content: bigwig
Library strategy: m6A-seq
 
Submission date Jun 20, 2023
Last update date Sep 20, 2023
Contact name Rui Li
E-mail(s) lirui@sysucc.org.cn
Organization name Sun Yat-sen University Cancer Center
Street address 651 Dongfeng East Road
City Guangzhou
ZIP/Postal code 510060
Country China
 
Platform ID GPL20795
Series (2)
GSE211588 CFL1-induced super enhancer RNA m6A modification promotes local chromatin accessibility and oncogenes transcription in pancreatic cancer [m6A-seq]
GSE211589 CFL1-induced super enhancer RNA m6A modification promotes local chromatin accessibility and oncogenes transcription in pancreatic cancer
Relations
BioSample SAMN35803699
SRA SRX20728657

Supplementary data files not provided
SRA Run SelectorHelp
Processed data are available on Series record
Raw data are available in SRA

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