|
Status |
Public on Oct 26, 2016 |
Title |
MCF10A FAIRE-seq input |
Sample type |
SRA |
|
|
Source name |
MCF10A FAIRE-seq input
|
Organism |
Homo sapiens |
Characteristics |
cell line: MCF10A cell type: Human breast cell line
|
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).
|
Extracted molecule |
genomic DNA |
Extraction protocol |
For FAIRE-seq, nuclei were extracted after the crosslinking step (1% formaldehyde in PBS) of intact cells, followed by re-suspension in SDS lysis buffer before sonication. FAIRE DNA samples were purified by phenol/chloroform extraction. Input DNA was also purified by phenol/chloroform extraction after the crosslinking was reversed. FAIRE-seq: Libraries were prepared according to Illumina's instructions (http://epigenome.usc.edu/services/nextgen/making_libraries.html)
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|
|
Library strategy |
FAIRE-seq |
Library source |
genomic |
Library selection |
other |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
FAIRE-seq reads were aligned to hg19 genome assembly using bwa.
For FAIRE-seq, Sole-Search (TF parameter, alpha value: 0.001, fdr: 0.001) was used to call peaks.
Genome_build: hg19
Supplementary_files_format_and_content: For FAIRE-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
|
Department |
Biochemistry and Molecular Medicine
|
Lab |
Rhie Lab
|
Street address |
1450 Biggy Street NRT 3504
|
City |
Los Angeles |
State/province |
CA |
ZIP/Postal code |
90089 |
Country |
USA |
|
|
Platform ID |
GPL11154 |
Series (1) |
GSE78913 |
Tracing Enhancer Networks using Epigenetic Traits (TENET) |
|
Relations |
BioSample |
SAMN05170550 |
SRA |
SRX1795460 |