|
Status |
Public on Aug 30, 2017 |
Title |
TAC_H3K27me3_rep2_ChIP-seq |
Sample type |
SRA |
|
|
Source name |
cardiomyocyte
|
Organism |
Mus musculus |
Characteristics |
strain: C57BL/6J chip antibody: anti-H3K27me3; Millipore (07-449) treatment: transverse aortic constriction (TAC) for 1 week
|
Extracted molecule |
genomic DNA |
Extraction protocol |
ChIP was performed as described elsewhere (Peters AH, et al. (2003) Mol Cell 12(6):1577–1589). The Libraries were generated using NuGEN Ovation Ultralow System V2 1–96 kit. ChIP-seq libraries were produced from as little as 1 ng of double-stranded DNA. The workflow is consisted of three steps: end repair to generate blunt ends, adaptor ligation with optional multiplexing and PCR amplification to produce the final library.
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|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2500 |
|
|
Description |
tac_H3K27me3.bw sham_tac_H3K27me3-diffpeaks-filt.bed
|
Data processing |
ChIP-seq reads were aligned to the mm10 genome assembly using bwa mem v0.7.10-r789 (PMID:19451168) Reads with mapping quality ≤ 10 and not properly paired were removed with samtools (v1.1) Differential peak calling was detected using THOR v0.1 (PMID: 27484474). The Input DNA signal was subtracted from each ChIP-seq signal. Differential peaks were filtered by adjusted pValue<= 0.01. Blacklisted regions identified by the ENCODE project (The ENCODE Project Consortium, 2012) were discarded during differential peaks detection and bigwig profile creation. Genome_build: mm10 (GRCm38) Supplementary_files_format_and_content: *.bw: the genomic distribution of ChIP-seq signal subtracted from the input DNA. These profiles were obtained using deeptools2 (PMID: 27079975) and these paramaters: -bs 10 --smoothLength 50 --ratio subtract --normalizeUsingRPKM. Supplementary_files_format_and_content: *.bed: list of the differential peaks called by THOR after filtering
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Submission date |
Jan 18, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Simone Serio |
E-mail(s) |
simone.serio@humanitasresearch.it
|
Organization name |
Humanitas Research Hospital
|
Department |
Cardiovascular Medicine
|
Street address |
Via Alessandro Manzoni, 56
|
City |
Rozzano |
State/province |
Milano |
ZIP/Postal code |
20089 |
Country |
Italy |
|
|
Platform ID |
GPL17021 |
Series (2) |
GSE93752 |
The genomic distribution of G9a, H3K9me2 and H3K27me3 in cardiac hypertrophy. |
GSE93754 |
The genomic distribution and gene expression profiling of cardiomyocyte-enriched populations |
|
Relations |
BioSample |
SAMN06237572 |
SRA |
SRX2499674 |