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Sample GSM4970534 Query DataSets for GSM4970534
Status Public on Jan 11, 2021
Title 5624_OXO
Sample type SRA
 
Source name proximal colon
Organism Mus musculus
Characteristics strain: 129S6/SvEvTac-Rag2tm1FwIl10-/-
treatment: sterile media
gender: male
Treatment protocol Mice aged 6-7 weeks received two doses every other day of 0.2 mL of 2 x 108 fresh inoculums (infected group) or sterile media (control group).
Growth protocol 129S6/SvEvTac-Rag2tm1FwIl10-/- (Rag2-/- / Il10-/-) mice were used and housed in an AAALAC-accredited specific pathogen-free barrier facility. Mice were maintained in polycarbonate microisolator caging (Allentown Caging Equipment Inc., Allentown, NJ) and provided pelleted diet (ProLab 3000, Purina Mills, St. Louis, MO) and filtered water ad libitum.
Extracted molecule genomic DNA
Extraction protocol Genomic DNA, total RNA were extracted from approximately 10 mg of proximal colon tissue using AllPrep DNA/RNA mini kit (QIAGEN, Hilden, Germany).
RRBS and oxRRBS libraries were prepared by Ovation® RRBS Methyl-Seq with TrueMethyl® oxBS kit (Tecan, Redwood City, CA) according to the manufacturer’s instructions.
 
Library strategy Bisulfite-Seq
Library source genomic
Library selection Reduced Representation
Instrument model NextSeq 550
 
Data processing Reduced representation bisulfite sequencing (RRBS) reads and oxRRBS reads were trimmed of low quality bases and adapter contamination with TrimGalore! 0.4.4_dev (http://www.bioinformatics. babraham.ac.uk/projects/trim_galore/) in paired-end mode, using Cutadapt version 1.8.1. (https://journal.embnet.org/index.php/embnetjournal/article/view/200). Any read pairs where one mate failed quality control were discarded.
Cleaned reads were aligned to the mouse mm10 genome with Bismark version 0.19.0. Resulting alignments were cleaned of PCR duplicates with NuDup (https://github.com/nugentechnologies/nudup), and reads with mapping quality of less than 20 were removed.
Analysis of methylated and hydroxymethylated regions followed the Methpipe analysis pipeline (commit 77d7728e6c52592a71706834d86f5e69183ef082 (Sept 7, 2018))
Genome-wide cytosines were filtered to represent only symmetrically methylated CpG sites. CpG sites that were not covered by at least 10 reads in each sample were discarded. CpG sites were further filtered to exclude sites that occurred within “blacklisted” regions of the mm10 genome assembly (ENCODE file ID ENCFF547MET).
Differentially methylated (DMR) and hydroxymethylated (DhMR) regions were identified by merging consecutive CpGs that crossed the threshold for statistical significance at a false discovery rate of 0.05, and filtering regions with at least three significant CpG sites.
Genome_build: mm10
Supplementary_files_format_and_content: Processed data are output from the methcount in the meth pipe analysis, which contains the chromosome location of the CpG sites, fraction numbers of 5mC+5hmC(BS dataset) or 5mC(oxBS dataset) and the corresponding coverage in each CpG site.
Supplementary_files_format_and_content: BS:5mC+5hmC fraction table
Supplementary_files_format_and_content: OXO:5mC fraction table
 
Submission date Dec 11, 2020
Last update date Jan 11, 2021
Contact name Qiyuan Han
E-mail(s) hanxx963@umn.edu
Organization name University of Minnesota
Street address 2231 6th St. Se, Tretyakova lab 2-230
City Minneapolis
State/province Minnesota
ZIP/Postal code 55455
Country USA
 
Platform ID GPL21626
Series (2)
GSE163037 Multi-omics characterization of inflammatory bowel disease induced hyperplasia/dysplasia in the Rag2-/- / Il10-/- mouse model [RRBS]
GSE163038 Multi-omics characterization of inflammatory bowel disease induced hyperplasia/dysplasia in the Rag2-/- / Il10-/- mouse model
Relations
BioSample SAMN17058527
SRA SRX9673791

Supplementary file Size Download File type/resource
GSM4970534_5624_OXO_Sym.meth.txt.gz 79.8 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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