LI Ng gIF ChIP Track Settings
 
Ludwig Institute/UCSD ChIP-chip NimbleGen - Gamma Interferon Experiments   (LI/UCSD ChIP)

This track is part of a parent called 'LI/UCSD ChIP'. To show other tracks of this parent, go to the LI/UCSD ChIP configuration page.

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    Interferon
            Untreated
            Treated
    Factor
            H3K4me2
            H3K4me3
            H3ac
            H4ac
            STAT1
            Pol2
    Signal/Peak
            Signal
            Peak
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dense
 LI H3K4me2 -gIF  Ludwig Institute/UCSD ChIP-chip Ng: HeLa, H3K4me2, no gamma interferon   schema 
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 LI H3K4me2 +gIF  Ludwig Institute/UCSD ChIP-chip Ng: HeLa, H3K4me2, 30 min after gamma interferon   schema 
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 LI H3K4me3 -gIF  Ludwig Institute/UCSD ChIP-chip Ng: HeLa, H3K4me3, no gamma interferon   schema 
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 LI H3K4m3 +gIF  Ludwig Institute/UCSD ChIP-chip Ng: HeLa, H3K4me3, 30 min after gamma interferon   schema 
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 LI H3ac -gIF  Ludwig Institute/UCSD ChIP-chip Ng: HeLa, H3ac, no gamma interferon   schema 
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 LI H3ac +gIF  Ludwig Institute/UCSD ChIP-chip Ng: HeLa, H3ac, 30 min after gamma interferon   schema 
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 LI H4ac -gIF  Ludwig Institute/UCSD ChIP-chip Ng: HeLa, H4ac, no gamma interferon   schema 
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 LI STAT1 +gIF  Ludwig Institute/UCSD ChIP-chip Ng: HeLa, STAT1, 30 min after gamma interferon   schema 
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 LI Pol2 -gIF  Ludwig Institute/UCSD ChIP-chip Ng: HeLa, Pol2, no gamma interferon   schema 
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 LI Pol2 +gIF  Ludwig Institute/UCSD ChIP-chip Ng: HeLa, Pol2, 30 min after gamma interferon   schema 
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 LI H3K4m2 -IF Pk  Ludwig Institute/UCSD ChIP-chip Ng Peak: HeLa, H3K4me2, no gamma interferon   schema 
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 LI H3K4m2 +IF Pk  Ludwig Institute/UCSD ChIP-chip Ng Peak: HeLa, H3K4me2, 30 min after gamma interferon   schema 
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 LI H3ac -gIF Pk  Ludwig Institute/UCSD ChIP-chip Ng Peak: HeLa, H3ac, no gamma interferon   schema 
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 LI H3ac +gIF Pk  Ludwig Institute/UCSD ChIP-chip Ng Peak: HeLa, H3ac, 30 min after gamma interferon   schema 
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 LI H4ac -gIF Pk  Ludwig Institute/UCSD ChIP-chip Ng Peak: HeLa, H4ac, no gamma interferon   schema 
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 LI STAT1 +gIF Pk  Ludwig Institute/UCSD ChIP-chip Ng Peak: HeLa, STAT1, 30 min after gamma interferon   schema 
    
Data version: ENCODE June & Oct 2005 Freezes
Data coordinates converted via liftOver from: May 2004 (NCBI35/hg17)

Description

This track displays results of the following ChIP-chip (NimbleGen) gamma interferon experiments on HeLa cells:

  • anti-H3K4me2, no gamma interferon
  • anti-H3K4me2, 30 minutes after gamma interferon
  • anti-H3K4me3, no gamma interferon
  • anti-H3K4me3, 30 minutes after gamma interferon
  • anti-H3ac, no gamma interferon
  • anti-H3ac, 30 minutes after gamma interferon
  • anti-H4ac, no gamma interferon
  • anti-STAT1, 30 minutes after gamma interferon
  • anti-RNA Pol2 in initiation complex, no gamma interferon
  • anti-RNA Pol2 in initiation complex, 30 minutes after gamma interferon

ENCODE region-wide location analysis of dimethylated K4 histone H3 (HK4me2 or diMeH3K4), trimethylated K4 histone H3 (H3K4me3 or triMeH3K4), RNA polymerase II, acetylated histone H3 (H3ac or AcH3), acetylated histone H4 (H4ac or AcH3) and STAT1 was conducted with ChIP-chip using chromatin extracted from HeLa cells induced for 30 minutes with gamma interferon as well as uninduced cells.

Methods

Chromatin from both induced and uninduced HeLa cells was separately cross-linked, precipitated with different antibodies, sheared, amplified and hybridized to an oligonucleotide tiling array produced by NimbleGen Systems. The array includes non-repetitive sequences within the 44 ENCODE regions tiled from NCBI Build 35 (UCSC hg17) with 50-mer probes at 38 bp interval.

For H3K4me3 and Pol2, intensity values for biological replicate arrays were combined after quantile normalization using R. The averages of the quantile normalized intensity values for each probe were then median-scaled and Loess-normalized using R to obtain the adjusted logR-values.

For all the other markers, each replicate was Loess-normalized and combined after intensity-based quantile normalization. The average log ratio for each probe was derived using linear model fitting with R. The peak positions were identified using the Mpeak program.

Verification

Three biological replicates were used to generate the track for each factor at each time point with the exception of RNA Pol2 uninduced, where only two biological replicates were used.

Credits

The data for this track were generated at the Ren Lab, Ludwig Institute for Cancer Research at UC San Diego.