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Sample GSM3106831 Query DataSets for GSM3106831
Status Public on Jun 15, 2019
Title ATAC-seq_human primary fetal astrocytes_rep2
Sample type SRA
 
Source name human primary fetal astrocytes
Organism Homo sapiens
Characteristics cell type: human primary fetal astrocytes
Growth protocol Human primary fetal astrocytes were cultured according to the ScienCell protocol (catalog #1801).
Extracted molecule genomic DNA
Extraction protocol Cells were harvested, snap frozen in dry ice, and stored at -80C. Cells were washed with ice cold PBS containing protease inhibitor and nuclei were extracted prior to library construction.
The standard ATAC-seq protocol was used, with the transposase reaction carried out for 30 minutes at 37C. 8-10 cycles of amplification were performed and dual size selection was performed with Ampure XP beads.
 
Library strategy ATAC-seq
Library source genomic
Library selection other
Instrument model Illumina HiSeq 4000
 
Description MS049
processed data file:
astrocyte.atac.seq.narrowPeak
astrocyte.atac-seq.bigwig
Data processing All reads were trimmed to 50 bp prior to processing. For libraries having undergone paired-end sequencing, only the first read was used.
All libaries were processed using the ENCODE ATAC-seq pipeline (December 2017).
Optimal IDR and optimal overlap peaks called by MACS2 were used.
Genome_build: hg19
Supplementary_files_format_and_content: Narrow peaks called using MACS2 and signal tracks in bigwig format
 
Submission date Apr 20, 2018
Last update date Jun 15, 2019
Contact name Yin Shen
E-mail(s) Yin.Shen@ucsf.edu
Phone 4155023403
Organization name UCSF
Department Department of Neurology
Lab Shen Lab
Street address 513 Parnassus Ave
City SAN FRANCISCO
State/province CALIFORNIA
ZIP/Postal code 94143-0410
Country USA
 
Platform ID GPL20301
Series (2)
GSE113480 Mapping cis-regulatory chromatin contacts in neural cells links neuropsychiatric disorder risk variants to target genes [ATAC-seq]
GSE113483 Mapping cis-regulatory chromatin contacts in neural cells links neuropsychiatric disorder risk variants to target genes
Relations
BioSample SAMN08965080
SRA SRX3981946

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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