NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1632684 Query DataSets for GSM1632684
Status Public on Mar 13, 2015
Title HPC5 Input tech rep 1 bio rep 2
Sample type SRA
 
Source name HPC5 cells
Organism Mus musculus
Characteristics cell type: Bone marrow derived hematopoietic progenitor cell line
strain: C57BL/6-cast (B6-cast)
Treatment protocol 10 million cells were cross-linked with 1% gluteraldehyde at room temperature for 10 minutes and quenched with 0.125 M glycine for 5 minutes.
Extracted molecule genomic DNA
Extraction protocol Cross-linked cells were lysed and sonicated to 200-500 bp fragments via bioruptor.
Chromatin fragments were incubated with the indicated biotinylated oligonucleotide probes and enriched material was selected by streptavidin magnet beads. Libraries were constructed using ThruPLEX-FD preparation kit (Rubicon, Ann Arbor, MI)
 
Library strategy OTHER
Library source genomic
Library selection other
Instrument model Illumina HiSeq 2500
 
Description technical replicate 1 of biological replicate 2
hpc5_CHIRP_con01_control_lambda.bw
library strategy: ChiRP-seq
Data processing Reads were mapped with Bowtie2. Uniquely mapped reads were used for peak calling by Macs2. Post-processing steps are described.
ChIRP-seq reads were aligned to the mm9 genome assembly using Bowtie2 version 2.0.6 with 1 mismatch in seed allowed, command=bowtie2 -p12 -k 2 -N 1. Peak calling was performed on uniquely aligned reads (lacking bowtie2 flag XS:i) with Macs2 version 2.0.10.20131216, command=macs2 callpeak -f BAMPE -g mm -m 2 50 --verbose 3 --bdg --SPMR -t treatment.bam -c control.bam , where treatment is RNA bound chromatin DNA and control is input DNA. Post-processing of peak data consisted of three steps. (1) Find concordant regions: Identify all possible regions of overlap among significant peaks called in the four LncHSC-2 and control LacZ experiments. (2) Remove non-specific regions: Exclude regions covered by LacZ peaks and regions not covered by concordant peaks in the two split-probe experiments. Require remaining regions to be covered by peaks in at least one of the two complete probe set experiments. (3) Select consensus peaks: Merge any overlapping regions, select the first intersecting peak from one of the two complete probe set experiments. Exclude the consensus peak if it has any overlap with LacZ peaks.
Genome_build: mm9
Supplementary_files_format_and_content: The narrowPeak are BED6+4 format file which contains the peak locations together with peak summit, pvalue and qvalue. Definition of some specific columns are: 5th: integer score for display, 7th: fold-change, 8th: -log10pvalue, 9th: -log10qvalue, 10th: relative summit position to peak start. The bigWig files were created from the Macs2 bedgraph files, representing signal density of fragment pileup as signal per million reads More information may be found in the Macs2 documentation.
 
Submission date Mar 12, 2015
Last update date May 15, 2019
Contact name deqiang sun
E-mail(s) dsun@tamu.edu
Phone (713) 677-7439
Organization name Texas A&M University
Street address 2121 W Holcombe Blvd
City Houston
State/province TX
ZIP/Postal code 77030
Country USA
 
Platform ID GPL17021
Series (2)
GSE63277 Long Non-coding RNAs Control Hematopoietic Stem Cell (HSC) Function
GSE66819 Long Non-coding RNAs Control Hematopoietic Stem Cell (HSC) Function (ChIRP-seq)
Relations
BioSample SAMN03402125
SRA SRX955674

Supplementary data files not provided
SRA Run SelectorHelp
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