GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
Sample GSM955113 Query DataSets for GSM955113
Status Public on Oct 26, 2012
Title MethylCap-seq_3T
Sample type SRA
Source name tumor colon tissue
Organism Homo sapiens
Characteristics technique: MethylCap-sequencing
starting molecule: genomic DNA
antibody/capture: Protein domain: His6–GST–MBD (Diagenode)
Treatment protocol No specific treatments
Extracted molecule genomic DNA
Extraction protocol MethylCap (Capturing of methylated DNA) was done using in automated procedure using a SX-8G/IP-StarTM robot (Diagenode). 2 µg of His6–GST–MBD (Diagenode) was incubated with 1 µg of fragmented DNA in binding buffer (BB, 20 mM Tris–HCl pH 8.5, 0.1% Triton X-100) with 200 mM NaCl in a final volume of 200 µl. This solution is mixed at 4 °C for 2 h. Magnetic GST-beads were prepared by washing 35 µl of a well-mixed beads suspension (Promega) with 200 µl of binding buffer + 200 mM NaCl at 4 °C. The suspension was mixed and a magnet was used to collect the beads. After removal of the supernatant the procedure is repeated once. After the second wash the supernatant is removed, but the beads are not allowed to get dry. The GST–MBD solution is added to the washed beads and this suspension is mixed for another hour at 4°C. After removal of the supernatant (the ‘flow-through’) the beads–GST–MBD–DNA complexes are washed/eluted. 200 µl of binding buffer with increasing concentrations of NaCl is added and the suspension is rotated for 10 min at 4 °C. Beads are captured on the magnet, and the supernatant is collected. Three different eluates were collected (LOW, MEDIUM, HIGH), corresponding 500 mM, 600 mM and 800 mM NaCl. For MethylCap-seq the MEDIUM and HIGH eluates were used separately.
Library strategy MBD-Seq
Library source genomic
Library selection MBD2 protein methyl-CpG binding domain
Instrument model Illumina Genome Analyzer IIx
Data processing Cluster generation and sequencing-by-synthesis (36 bp) was performed using the Illumina Genome Analyzer IIx (GAIIx) platform according to standard protocols of the manufacturer (Illumina). The image files generated by the Genome Analyzer were processed to extract DNA sequence data. Sequence reads were aligned to the human (hg18) reference genome using the Illumina Analysis Pipeline allowing, one mismatch. Only the 36 bp sequence reads uniquely aligning to the genome were considered for further analysis. The output data were converted to Browser Extensible Data (BED) files for downstream analysis and Wiggle (WIG) files for viewing the data in the UCSC Genome Browser. All sequence analyses were conducted based on the Homo Sapiens hg18 genome assembly.
Genome_build: hg18
Supplementary_files_format_and_content: The file "MergedPeaks_normalized_tagdensity.gz" contains processed data for all patient samples. It is a tab-delimited text file. MethylCap-seq was performed on 24 micro-dissected tumors and an equal number of matched microscopically normal tissue samples (48 DNA methylation profiles in total). Enriched regions (peaks) were called for each sample on the basis of a Poisson distribution of overlapping sequence reads within a dynamic window. A false discovery rate (FDR) was calculated relative to the total covered sequence, and peaks with an FDR of ≤10-6 were selected. All peaks from the 48 samples were merged. Per sample the number of tags overlapping each region of interest was calculated and normalized by dividing by the total number of aligned reads of the sample, and the length of the peak.
Submission date Jul 03, 2012
Last update date May 15, 2019
Contact name Arjen Brinkman
Organization name Radboud University, Nijmegen Center for Molecular Life Sciences
Department Molecular Biology
Lab Stunnenberg
Street address NCMLS #274, Geert Grooteplein Zuid 30
City Nijmegen
ZIP/Postal code 6525 GA
Country Netherlands
Platform ID GPL10999
Series (1)
GSE39068 Comparative genome-wide DNA methylation analysis of colorectal tumor and matched normal tissues
SRA SRX157359
BioSample SAMN01085228

Supplementary file Size Download File type/resource
GSM955113_3T.reads.bed.gz 152.0 Mb (ftp)(http) BED
GSM955113_3T.wig.gz 11.2 Mb (ftp)(http) WIG
SRA Run SelectorHelp
Processed data provided as supplementary file
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap