|
Status |
Public on Aug 27, 2019 |
Title |
Experiment A - 0.6 units AluI |
Sample type |
SRA |
|
|
Source name |
Experiment A - 0.6 units AluI
|
Organism |
Mus musculus |
Characteristics |
strain: NIH/S gender: Female age: E13.5 tissue: liver treatment: 0.6 units AluI
|
Treatment protocol |
Nuclei were prepared from homogenised liver and digested with increasing amounts of the restriction enzyme AluI.
|
Growth protocol |
Livers were dissected from female NIH/S mice (E13.5) and stored at -80C.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
AluI digestion was stopped and the DNA was sonicated. Purified sonicated DNA was prepared for Illumina paired-end sequencing using New England Biolabs kit E7370. 50-nt paired reads were obtained using an Illumina NextSeq-500 machine. New method: Quantitative DNA accessibility assay - "qDA-seq"
|
|
|
Library strategy |
OTHER |
Library source |
genomic |
Library selection |
other |
Instrument model |
Illumina NextSeq 500 |
|
|
Description |
HepD-2_A3
|
Data processing |
Sequences were aligned to the Mus musculus genome (mm10) using Bowtie2 with the parameters -X 5000 --very-sensitive For every AluI motif (AGCT) found in the genome, we estimated the fraction of nuclei in which the given motif was cleaved by AluI, f_cut = N_cut=(N_cut + N_uncut), by counting the number of reads that were cut at this site (with an end at this site), N_cut, and the number of reads that were not cut at this site (overlapping the motif), N_uncut, using the Bioinformatics toolbox from Matlab. Genome-wide profiles (bw files) containing the fraction of cut DNA at each site were generated using Matlab and wigToBigWig. Genome_build: mm10 Supplementary_files_format_and_content: bigwig files containing the fraction of cut DNA at each AluI site along the mouse genome (for IGV genome browser)
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|
|
Submission date |
Jun 12, 2018 |
Last update date |
Aug 27, 2019 |
Contact name |
Razvan V. Chereji |
E-mail(s) |
razvan.chereji@nih.gov
|
Phone |
301-435-8670
|
Organization name |
National Institutes of Health
|
Department |
NICHD
|
Lab |
David J. Clark Lab
|
Street address |
6 Center Drive, Room 2A14
|
City |
Bethesda |
State/province |
Maryland |
ZIP/Postal code |
20892 |
Country |
USA |
|
|
Platform ID |
GPL19057 |
Series (2) |
GSE115691 |
DNA accessibility is not the primary determinant of chromatin-mediated gene regulation (mouse) |
GSE115693 |
DNA accessibility is not the primary determinant of chromatin-mediated gene regulation |
|
Relations |
BioSample |
SAMN09402746 |
SRA |
SRX4199242 |