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Sample GSM6970179 Query DataSets for GSM6970179
Status Public on Nov 08, 2023
Title ChIP-seq_p14_rhom_input1
Sample type SRA
 
Source name Retina
Organism Mus musculus
Characteristics tissue: Retina
strain: C57BL/6
genotype: CrxR90W/W
developmental stage: Post-natal day 14
chip antibody: none
Extracted molecule genomic DNA
Extraction protocol Pooled nuclear extracts from 6 retinae were cross-linked with formaldehyde prior to immunoprecipitation with anti-CRX antibody. Input controls were generated with normal rabbit IgG. The libraries were prepared following the standard ChIP-seq protocol (Schmidt et al., 2014)
ChIP-seq libraries were prepared for sequencing using standard Illumina protocols.
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina NovaSeq 6000
 
Data processing For each sample, reads from two sequencing lanes were first concatenated and trimmed with Trim Galore (v0.6.1).
The trimmed reads were then mapped to the mm10 genome using Bowtie2 (v 2.3.4.1) with parameters -X 2000 --very-sensitive.
Only uniquely mapped and properly paired reads were retained with samtools (v1.9) with parameters -f 0x2 -q 30.
Mitochondria reads were removed with samtools (v1.9). Duplicated reads were marked and removed with Picard (v2.21.4).
Last, reads mapped to the mm10 blacklist regions were removed by bedtools (v2.27.1) by intersect -v.
Assembly: mm10
Supplementary files format and content: bigWig files generated with deeptools (v3.0.0). Scores represent CPM values at 10bp binsize.
Supplementary files format and content: narrowPeak files generated by MACS2 (v2.1.1.20160309) callpeak with default parameters
 
Submission date Jan 24, 2023
Last update date Nov 08, 2023
Contact name Yiqiao Zheng
E-mail(s) yiqiao.zheng@wustl.edu
Phone 314-747-4351
Organization name Washington University in St Louis
Department Department of Ophthalmology & Visual Sciences
Lab Shiming Chen, Ph.D.
Street address 517 South Euclid Avenue
City Saint Louis
State/province Missouri
ZIP/Postal code 63110
Country USA
 
Platform ID GPL24247
Series (2)
GSE223657 Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms [ChIP-seq]
GSE223659 Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms
Relations
BioSample SAMN32901342
SRA SRX19164889

Supplementary file Size Download File type/resource
GSM6970179_r1_input.sorted.blk.bigWig 167.6 Mb (ftp)(http) BIGWIG
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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