|
Status |
Public on Nov 28, 2017 |
Title |
ATACseq-Patski-WT |
Sample type |
SRA |
|
|
Source name |
Patski cells
|
Organism |
Mus musculus x Mus spretus |
Characteristics |
cell line: Patski cell type: Fibroblasts derived from hybrid embryonic kidney strain/background: BL6/spretus genotype/variation: wild-type
|
Extracted molecule |
genomic DNA |
Extraction protocol |
ATAC-seq was done on WT, Del-hinge, Inv-Dxz4 and 2-4-clone Patski cells using a published method.
|
|
|
Library strategy |
ATAC-seq |
Library source |
genomic |
Library selection |
other |
Instrument model |
Illumina NextSeq 500 |
|
|
Description |
ATAC-seq experiment in wild-type Patski cells.
|
Data processing |
ATAC-seq paired-end reads were mapped to the BL6 genome using the NCBI build v38/mm10 reference genome assembly obtained from the UCSC Genome Browser46 using BWA-MEM (v0.7.3) in paired-end mode using default parameters. Primary mapped valid paired reads with MAPQ>=10 were de-duplicated and used for calling ATAC peaks based on biallelic reads using MACS2. ATAC peaks were called using all reads (unsegregated). Genome_build: mm10 (GRCm38) Supplementary_files_format_and_content: bed, xls
|
|
|
Submission date |
Nov 22, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Xinxian Deng |
E-mail(s) |
dengx2@u.washington.edu
|
Organization name |
University of Washington
|
Department |
Laboratory Medicine and Pathology
|
Lab |
HSB C526
|
Street address |
1959 NE Pacific St.
|
City |
Seattle |
State/province |
WA |
ZIP/Postal code |
98195 |
Country |
USA |
|
|
Platform ID |
GPL20213 |
Series (2) |
GSE59779 |
Studies of regulation of mouse X inactivation and genes escaping XCI |
GSE107290 |
An evaluation of the effects of CRISPR/cas9-mediated editing of the Dxz4 locus on regulation of the mouse inactive X chromosome in Patski cells [ATAC-seq] |
|
Relations |
BioSample |
SAMN08092868 |
SRA |
SRX3418102 |