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Status |
Public on Oct 26, 2016 |
Title |
H3K27Ac ChIP-seq MCF10A rep1 |
Sample type |
SRA |
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Source name |
H3K27Ac ChIP-seq MCF10A
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Organism |
Homo sapiens |
Characteristics |
cell line: MCF10A cell type: Human breast cell line chip antibody: H3K27Ac Abcam ab4729
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Growth protocol |
The immortalized human normal breast cell line MCF10A (ATCC # CRL-10317) was maintained in DMEM/F12 with 5% horse serum, 100units/ml penicillin, 0.1mg/ml streptomycin, 0.5ug/ml hydrocortisone, 100ng/ml cholera toxin, 10ug/ml insulin, and 20ng/ml epidermal growth factor (EGF).
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Extracted molecule |
genomic DNA |
Extraction protocol |
For ChIP-seq, cells were crosslinked using 1% formaldehyde and lysates were clarified from sonicated nuclei and histone-DNA complexes were isolated with antibody. ChIP-seq: Libraries were barcoded (NEXTflex™ DNA Barcodes) (Bio Scientific, Austin, TX).
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Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2000 |
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Data processing |
ChIP-seq reads were aligned to hg19 genome assembly using bwa.
For ChIP-seq, Sole-Search (alpha=0.0001, FDR=0.0001, peakmergedistance=0, histoneblurlength=1200) was used to call peaks.
Genome_build: hg19
Supplementary_files_format_and_content: For ChIP-seq, tab-delimited text files include location of peaks
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Submission date |
May 24, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Suhn K Rhie |
Organization name |
University of Southern California
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Street address |
1450 Biggy Street
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City |
Los Angeles |
State/province |
CA |
ZIP/Postal code |
90089 |
Country |
USA |
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Platform ID |
GPL11154 |
Series (1) |
GSE78913 |
Tracing Enhancer Networks using Epigenetic Traits (TENET) |
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Relations |
BioSample |
SAMN05170551 |
SRA |
SRX1795461 |
Supplementary file |
Size |
Download |
File type/resource |
GSM2175781_SS_MCF10A_H3K27Ac_rep1.txt.gz |
593.4 Kb |
(ftp)(http) |
TXT |
SRA Run Selector![Help](/coreweb/images/long_help4.gif) |
Raw data are available in SRA |
Processed data provided as supplementary file |
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