|
Status |
Public on Jul 14, 2014 |
Title |
NCCIT siEED+siRNF2 5mC-seq |
Sample type |
SRA |
|
|
Source name |
NCCIT human cells depleted of EED and RNF2 by siRNA
|
Organism |
Homo sapiens |
Characteristics |
cell line: NCCIT cell type: human embryonic carcinoma cells transfected with: siRNA against EED and RNF2 transcripts affinity purification method: MethylMagnet mCpG DNA isolation (Ribomed)
|
Growth protocol |
NCCIT cells were cultured in McCoy’s 5A medium (Invitrogen) supplemented with 2 mm L-glutamine (Mediatech) and 10% heat-inactivated fetal bovine serum (Hyclone).
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Genomic DNA was isolated by proteinase digestion and phenol:chloroform extraction. Affinity purification was performed according to manufacturers' protocols. DNA sequencing libraries were constructed according to Illumina's protocol for TruSeq DNA sample preparation kit
|
|
|
Library strategy |
MBD-Seq |
Library source |
genomic |
Library selection |
MBD2 protein methyl-CpG binding domain |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
Basecalls performed using CASAVA version 1.8 MBD-seq reads were aligned to the hg19 genome assembly using BWA version 0.5.9. Mapped reads were filtered if they were mapped to multiple locations and to unique location with 5% or more mismatches and indels of read lengths. peaks were called using SICER version 1.1 with the following setting: Window Size (200),Gap Size (400), Effective genome size (0.833). differential peaks were called using SICER version 1.1 with the following setting: Window Size (200),Gap Size (400), Effective genome size (0.833). Genome_build: hg19 Supplementary_files_format_and_content: bigwig files were generated using wigToBigWig; Scores represent read depth.
|
|
|
Submission date |
Apr 07, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Keith D Robertson |
E-mail(s) |
robertson.keith@mayo.edu
|
Phone |
507-266-4886
|
Organization name |
Mayo Clinic
|
Department |
Molecular Pharmacology & Experimental Therapeutics
|
Lab |
Epigenetic Etiology of Human Disease Laboratory
|
Street address |
200 First Street SW, Stabile 12-70
|
City |
Rochester |
State/province |
MN |
ZIP/Postal code |
55905 |
Country |
USA |
|
|
Platform ID |
GPL11154 |
Series (2) |
GSE56538 |
Impact of human MLL/COMPASS and Polycomb complexes on the DNA methylome [MBD-seq] |
GSE56539 |
Impact of human MLL/COMPASS and Polycomb complexes on the DNA methylome |
|
Relations |
BioSample |
SAMN02720886 |
SRA |
SRX512191 |
Named Annotation |
GSM1363484_EEDRNF2.bigwig |