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SRX3643709: GSM2977255: Mock_STAT2_ChIP-seq; Homo sapiens; ChIP-Seq
1 ABI_SOLID (AB 5500xl Genetic Analyzer) run: 19.8M spots, 989.9M bases, 557.6Mb downloads

Submitted by: NCBI (GEO)
Study: Genome-wide maps of STAT1, STAT2 and IRF9 in conjunction with nucleosome occupancy maps at 20 interferon-stimulated gene regions during steady state and after type I interferon stimulation.
show Abstracthide Abstract
The genome-wide distributions of STAT1, STAT2 and IRF9 in mock and interferon alpha (IFN) stimulated human cells was generated using high throughput sequencing to identify ISGF3 genomic occupancy. In combination, the nucleosome occupancy of 20 select IFN-stimulated gene regions were analyzed by direct selection MNase sequencing to determine the nucleosome positions and changes in nucleosome occupancy levels following IFN treatment over time. IFN stimulation resulted in decreased nucleosome positioning strength, with clear disruption over the course of IFN treatment followed by a return to steady state, and prominently at most ISGF3-bound regions. Overall design: Examination of 3 proteins genome-wide and nucleosome occupancy at 20 interferon-stimulated gene regions during steady state and after type I interferon stimulation in 1 human cell line.
Sample: Mock_STAT2_ChIP-seq
SAMN08457514 • SRS2908904 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: AB 5500xl Genetic Analyzer
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: SINGLE
Construction protocol: For ChIP-seq: Lysates were clarified sonicated nuclei and STAT1, STAT2, and IRF9 was immunoprecipitated with the corresponding antibody. For Direct selection MNase-seq: Mononucleosomes were isolated following MNase digestion and direct selection via bacterial artificial chromosome hybridization isolation. Libraries were prepared using the 5500 Series SOLiD Systems Fragment Library Preparation protocol using the ABI library preparation kit or NEBNext kit. The fragmented DNA was blunt-ended, size selected for 100-250 bp using Agencourt AMPure XP reagent, and then adding a dA tail for ligation with SOLiD adaptors. The adaptor-ligated DNA was purified using Agencourt AMPure XP reagent and PCR-amplified for 13-15 cycles. The quantity and size was verified using the Bioanalyzer .
Experiment attributes:
GEO Accession: GSM2977255
Links:
Runs: 1 run, 19.8M spots, 989.9M bases, 557.6Mb
Run# of Spots# of BasesSizePublished
SRR666684819,798,334989.9M557.6Mb2018-07-26

ID:
5042435

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