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Status |
Public on Jan 21, 2009 |
Title |
naïve-H3K27me3 |
Sample type |
SRA |
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Source name |
Naive cells
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Organism |
Mus musculus |
Characteristics |
naïve-H3K27me3
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Treatment protocol |
Treatment protocol as described in Wei et al., 2009 (PMID:19144320)
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Growth protocol |
Growth protocol as described in Wei et al., 2009 (PMID:19144320)
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Extracted molecule |
genomic DNA |
Extraction protocol |
Extract protocol as described in Wei et al., 2009 (PMID:19144320)
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Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina Genome Analyzer |
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Description |
Chromatin IP T cells were treated with MNase to generate approximately 80% mononucleosomes and 20% dinucleosomes. Chromatin from 2 × 107 cells was used for each ChIP experiment, which yielded approximately 100 ng of DNA. Antibodies against histone H3K4me3 (ab8580, Abcam) and H3K27me3 (07-449, Upstate) were used. The ChIP DNA fragments were blunt-ended, ligated to the Solexa adaptors, and sequenced with the Illumina 1G Genome Analyzer.
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Data processing |
Sequence reads were obtained and mapped to the mouse (February, 2006) genomes using the Illumina Genome Analyzer Pipeline. More details as described in Wei et al., 2009 (PMID:19144320)
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Submission date |
Jan 21, 2009 |
Last update date |
May 15, 2019 |
Contact name |
Weiqun Peng |
E-mail(s) |
wpeng@gwu.edu
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Organization name |
The Georege Washington University
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Street address |
725 21st street, NW
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City |
DC |
ZIP/Postal code |
20052 |
Country |
USA |
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Platform ID |
GPL9185 |
Series (1) |
GSE14254 |
Global Mapping of Histone H3 K4 and K27 Trimethylation: Lineage Fate Determination of Differentiating CD4+ T Cells |
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Relations |
SRA |
SRX003808 |
BioSample |
SAMN02195434 |
Named Annotation |
GSM361998.bed.gz |
Supplementary file |
Size |
Download |
File type/resource |
GSM361998.bed.gz |
106.6 Mb |
(ftp)(http) |
BED |
SRA Run Selector |
Processed data provided as supplementary file |
Raw data are available in SRA |
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