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Sample GSM983097 Query DataSets for GSM983097
Status Public on Jan 22, 2013
Title H3122_input
Sample type SRA
 
Source name H3122_input
Organism Homo sapiens
Characteristics cell line: NCI-H3122
antibody: none
Growth protocol RPMI1640 +10% FBS
Extracted molecule genomic DNA
Extraction protocol Crosslinked with 1% formaldehyde, washed with PBS, lysed in lysis buffer (1% SDS, 10mM EDTA, 50mM Tris-HCl, pH 8.0), sonicated with Covaris E210 to shear DNA to 200-1500bp. After immunoprecipitation or without immunoprecipitation for input, beads were washed, RNase A and Proteinase K treated and reverse crosslinked in elution buffer (1% SDS, 0.1M NaHCO3). DNAs were column purified and subjected to standard Illumina library construction.
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina Genome Analyzer IIx
 
Description Input
Data processing Bowtie alignment (H1819, H2087, H3122_2, H3122_FOXA1_ab23738) or GenePAST alignment (H3122_input and H3122_NKX2-1_BL4000)
read counts normalization in 100kb window size
Peak calling (MACS 1.4.0)
Genome_build: hg18
Supplementary_files_format_and_content: bed
 
Submission date Aug 08, 2012
Last update date May 15, 2019
Contact name Hideo Watanabe
E-mail(s) hideo.watanabe@mssm.edu
Organization name Icahn School of Medicine at Mount Sinai
Department Department of Medicine, Division of Pulmonary, Critical Care and Sleep Medicine
Lab Hideo Watanabe
Street address One Gustave L. Levy Place
City New York
State/province NY
ZIP/Postal code 10029
Country USA
 
Platform ID GPL10999
Series (1)
GSE39998 NKX2-1 occupancy in human lung adenocarcinoma cell lines
Relations
SRA SRX174812
BioSample SAMN01109519

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data not applicable for this record

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