|
Status |
Public on Jan 24, 2018 |
Title |
WGBS in AtT-20 expressing Neo |
Sample type |
SRA |
|
|
Source name |
AtT-20 cells expressing 3x flag-Neo
|
Organism |
Mus musculus |
Characteristics |
cell type: pituitary corticotroph cell passages: 10-20 cell line: AtT-20 cells treatment: non treated : Bisulfite conversion
|
Growth protocol |
AtT-20 cells were plated on adherent culture dishes to obtain about 70% confluence after 3 days. They are cultured in DMEM + 10% FBS.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Genomic DNA was extracted from 1,000,000 cells and bisulfite conversion was performed with the Zymo Research EZ DNA Methylation- Lightning Kit. Libraries were prepared according to Illumina's instructions. Libraries were sequenced on the Illumina Hi-seq 2000 following the manufacturer's protocols to obtain 100bp paired end reads.
|
|
|
Library strategy |
Bisulfite-Seq |
Library source |
genomic |
Library selection |
RANDOM |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
Sequence reads were trimmed for adapter sequences. The resulting 100bp reads were mapped to thebisulfite converted reference genome GRCm38 with bismarck. After alignement, we removed duplicate reads. Genome_build: mm10 Supplementary_files_format_and_content: Differential methylation analsysis was performed using methylkit
|
|
|
Submission date |
Sep 21, 2016 |
Last update date |
May 15, 2019 |
Contact name |
ALEXANDRE MAYRAN |
E-mail(s) |
alexandre.mayran@epfl.ch
|
Organization name |
EPFL
|
Street address |
Station 19
|
City |
LAUSANNE |
State/province |
Waadt |
ZIP/Postal code |
1015 |
Country |
Switzerland |
|
|
Platform ID |
GPL13112 |
Series (2) |
GSE87184 |
Whole Genome Bisulfite Sequencing in Pax7-reprogrammed corticotropes AtT-20 cells |
GSE87185 |
Pioneer factor Pax7 deploys a stable enhancer repertoire for specification of cell fate |
|
Relations |
BioSample |
SAMN05799349 |
SRA |
SRX2183005 |