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Status |
Public on Nov 17, 2014 |
Title |
Input DNA |
Sample type |
SRA |
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Source name |
HEK293 Cells
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Organism |
Homo sapiens |
Characteristics |
antibody 1: none antibody 2: none cell line: HEK293 cell type: embryonic kidney
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Growth protocol |
HEK293 were grown under standard tissue culture conditions
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Extracted molecule |
genomic DNA |
Extraction protocol |
Lysates were clarified from sonicated HEK293 nuclei and histone-DNA complexes were isolated with anti-DDX21 antibody. Libraries were prepared according to NEBNext kit.
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Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2500 |
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Data processing |
ChIP-seq reads were aligned to the hg19 genome assembly using DNANexus peaks were called using QuEST with the following setting: ChIP estimate threshold (20),ChIP extension fold enrichment (3), and a ChIP-to-background fold enrichment (3) Genome_build: hg19
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Submission date |
Apr 15, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Ryan Alexander Flynn |
E-mail(s) |
raflynn@stanford.edu
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Organization name |
Stanford University
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Street address |
380 Roth Way, Room 265
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City |
Stanford |
State/province |
CA |
ZIP/Postal code |
94305 |
Country |
USA |
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Platform ID |
GPL16791 |
Series (1) |
GSE56802 |
RNA helicase DDX21 coordinates transcription and noncoding RNA processing of the ribosomal pathway |
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Relations |
BioSample |
SAMN02727890 |
SRA |
SRX952173 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data not provided for this record |
Processed data are available on Series record |
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