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Status |
Public on Mar 31, 2022 |
Title |
si-N6AMT1 6mA-IP-seq rep2 |
Sample type |
SRA |
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|
Source name |
breast cancer cell lines
|
Organism |
Homo sapiens |
Characteristics |
cell line: MDA-MB-453 6ma-ip-seq antibody: 6mA antibodies (Synaptic Systems)
|
Treatment protocol |
siRNA (10 nM) targeting human N6AMT1 and scramble siRNA (Control) were transfected into MDA-MB-453 cells using Lipofectamine RNAiMAX Transfection Reagent (Invitrogen) for 48 hours.
|
Growth protocol |
MDA-MB-453 cells were cultured in DMEM growth medium supplemented with 10% FBS, 1% 100x penicillin-streptomycin-amphotericin B, and 1% 100x nonessential amino acid solution in a humidified incubator at 37°C with 5% carbon dioxide.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Genomic DNA was extracted from cultured cells via a TIANamp Genomic DNA Kit (Tiangen Biotech, China). To exclude contaminating RNA, the genomic DNA was treated with 0.1 mg/ml RNase A. Six libraries (two biological replicates each for immune-precipitated DNA and their input) were prepared using a NovaSeq 6000 S4 Reagent Kit (300 cycles) according to the manufacturer’s instructions
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|
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Library strategy |
MeDIP-Seq |
Library source |
genomic |
Library selection |
5-methylcytidine antibody |
Instrument model |
Illumina NovaSeq 6000 |
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Data processing |
The high quality of reads was aligned to the human reference genome (hg19) by bowtie2 (v2.3.5) (PMID: 22388286). Duplicated reads were removed by samtools (v1.9). 6mA methylated regions were identified with MACS2 with parameters -p 1e-5. Genome_build: hg19 Supplementary_files_format_and_content: peak text files
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Submission date |
Feb 10, 2021 |
Last update date |
Mar 31, 2022 |
Contact name |
Ping Wang |
E-mail(s) |
pingwangwp@gmail.com
|
Organization name |
Tianjin Medical University
|
Street address |
No22.Qixiangtai Rd.,Heping Dist
|
City |
Tianjin |
ZIP/Postal code |
300000 |
Country |
China |
|
|
Platform ID |
GPL24676 |
Series (2) |
GSE166580 |
Reduction N6AMT1-mediated 6mA DNA modification promotes tumor progression [MeDIP-seq] |
GSE166582 |
Reduction N6AMT1-mediated 6mA DNA modification promotes tumor progression |
|
Relations |
BioSample |
SAMN17861046 |
SRA |
SRX10070654 |