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Sample GSM8229478 Query DataSets for GSM8229478
Status Public on Apr 28, 2024
Title WGBS, 2205 in vitro, DMSO, Replicate 3
Sample type SRA
 
Source name cholangiocarcinoma
Organism Mus musculus
Characteristics tissue: cholangiocarcinoma
cell line: 2205
cell type: tumor cells
genotype: Albumin-Cre; KrasG12D; IDH1R132C
treatment: DMSO
Treatment protocol This study used the mIDH inhibitor, AG120 (Servier Pharmaceuticals). Murine ICC (2205) cells were treated for five days with either DMSO or 1 μM mIDH inhibitor (AG120). Where indicated, 10ng/mL IFNγ was added for the final two days of culturing. The normal livers were from vehicle- or AG120-treated mice for 6 days.
Growth protocol Murine IDH1R132C ICC cell line (2205) were cultured in RPMI 1640 (+) L-glutamine, 25 mmol/L HEPES containing 10% FBS and 1% penicillin–streptomycin.
Extracted molecule genomic DNA
Extraction protocol Genomic DNAs from single-cell suspensions from cells cultured in a monolayer or liver tissues were extracted from homogenized samples using the QIAamp DNA Mini Kit in accordance with the manufacturer’s suggested protocol.
EZ DNA Methylation Gold Kit (Zymo Research) for DNA bisulfite conversion and Accel-NGS® Methyl-Seq DNA Library Kit for lib prep
 
Library strategy Bisulfite-Seq
Library source genomic
Library selection RANDOM
Instrument model Illumina NovaSeq 6000
 
Data processing Adapter sequences were trimmed using Trimmomatic (v0.36).
Pre- and post- trimming quality control was done using FastQC (v0.11.7).
Bismark (v0.24.0, Babraham Bioinformatics, wrapper around Bowtie2) was used to align reads to the mm10 genome with default parameters.
The Bismark function deduplicate_bismark was used to remove read duplicates from alignment files.
The bismark_methylation_extractor function was used to quantify methylated sites with the parameters “-p --comprehensive --no_overlap –bedgraph”.
Assembly: mm10
Supplementary files format and content: COV files outputted by bismark which has percent methylation and methylated and total read counts for each CpG
 
Submission date Apr 24, 2024
Last update date Apr 28, 2024
Contact name Robert Manguso
E-mail(s) rmanguso@broadinstitute.org
Organization name Broad Institute of MIT and Harvard
Street address 75 Ames Street
City Cambridge
State/province MA
ZIP/Postal code 02142
Country USA
 
Platform ID GPL24247
Series (2)
GSE264730 Mutant IDH1 inhibition induces dsDNA sensing to activate tumor immunity
GSE265806 Mutant IDH1 inhibition induces dsDNA sensing to activate tumor immunity [mouse WGBS]
Relations
BioSample SAMN41074573
SRA SRX24360765

Supplementary file Size Download File type/resource
GSM8229478_2205_V3.bismark.cov.gz 227.0 Mb (ftp)(http) COV
SRA Run SelectorHelp
Raw data are available in SRA

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