Figure 1 in few minutes
Step by step guide
Data processing
●Go to the main page of EpiExplorer
http://epiexplorer.mpi-inf.mpg.de
●Copy the ID d_5hmChotspotsSzulwachetal_330832
●Click on Reload icon
●Paste the ID in the box and press enter
http://epiexplorer.mpi-inf.mpg.de/index.php?userdatasets=d_5hmChotspotsSzulwachetal_330832
Figure 1A, Summary
● Press on the Select button next to the dataset
●From Select overlap criterion: select Any overlap
●From Select tissue: select H1-hESC
http://epiexplorer.mpi-inf.mpg.de/index.php?analysisLink=97970e9d78899056e761caa64403db21
Figure 1B, H3K4me1 overlap, 1/2
●Activate the control
○ Press back button
■Copy the control set
ID d_5hmChotspotsSzulwachetal_ref_330832
■ Click on Reload icon
■Paste the ID in the box and press enter
○ Press the Compare button next to Control for 5hmC
hotspots Szulwach
○ Press Select on the 5hmC hotspots
Szulwach dataset
Figure 1B, H3K4me1 overlap, 2/2
●Press on Histone modifications (ENCODE)
●Press on H3K4me1
http://epiexplorer.mpi-inf.mpg.de/index.php?analysisLink=a04f8f18d4cb2bf01d3aba9844060154
Figure 1C, H3K4me1 neighborhood
● Press on the remove button on the right of Control set
Regions
●Press on Neighborhood under H3K4me1
●(Press on "any" tissue in the figure legend)
http://epiexplorer.mpi-inf.mpg.de/index.php?analysisLink=bf53fac474af2214ea81d6c189ba9ac9
Figure 1D, Predicted genome elements
●Activate the control set (see Figure 1B, 1/2)
●Press on Chromatin state segmentation
http://epiexplorer.mpi-inf.mpg.de/index.php?analysisLink=00b780b85cedb266a306cd04ce83781d
Figure 1E, DNA methylation
●Press on to "unlock" the comparison. (After that, every
refinement applied to the main dataset will also be applied to
the reference. See the dedicated slideshow for more info)
●Press on DNA methylation (ROADMAP)
●Then on hES_H1_p38
●Then on Number of observed CpGs
●Move the left handle of the slider to 5
●Press on Filter to this selection
●Press on Average CpG methylation ratio
http://epiexplorer.mpi-inf.mpg.de/index.php?analysisLink=13221a5d490ccc3c572281f4ba5e5d9f
Figure 1F, Gene Ontology terms, 1/2
●Press to remove the Number of CpGs refinement from
1E
●Press to remove the control dataset
●Now, you have reset the dataset to its initial state
●Press on Region score
●Slide the left handle of the slider till 200
●Press the Filter to this selection button
●Press on Genes and annotations
●Press on Gene ontology (terms)
●Above the visualization, select 50 from the drop-down menu
next to "Exclude GO terms matching less than N genes"
●Above the visualization, select 5,100 from the drop-down
menu next to "Exclude GO terms matching more than N
genes"
●Press twice on the header of the column Ratio
Figure 1F, Gene Ontology terms, 2/2
http://epiexplorer.mpi-inf.mpg.de/index.php?analysisLink=5e950bb28c67d937617b358e910667c5
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EpiExplorer: Step by step guide to figure 1

  • 1.
    Figure 1 infew minutes Step by step guide
  • 2.
    Data processing ●Go tothe main page of EpiExplorer http://epiexplorer.mpi-inf.mpg.de ●Copy the ID d_5hmChotspotsSzulwachetal_330832 ●Click on Reload icon ●Paste the ID in the box and press enter http://epiexplorer.mpi-inf.mpg.de/index.php?userdatasets=d_5hmChotspotsSzulwachetal_330832
  • 3.
    Figure 1A, Summary ●Press on the Select button next to the dataset ●From Select overlap criterion: select Any overlap ●From Select tissue: select H1-hESC http://epiexplorer.mpi-inf.mpg.de/index.php?analysisLink=97970e9d78899056e761caa64403db21
  • 4.
    Figure 1B, H3K4me1overlap, 1/2 ●Activate the control ○ Press back button ■Copy the control set ID d_5hmChotspotsSzulwachetal_ref_330832 ■ Click on Reload icon ■Paste the ID in the box and press enter ○ Press the Compare button next to Control for 5hmC hotspots Szulwach ○ Press Select on the 5hmC hotspots Szulwach dataset
  • 5.
    Figure 1B, H3K4me1overlap, 2/2 ●Press on Histone modifications (ENCODE) ●Press on H3K4me1 http://epiexplorer.mpi-inf.mpg.de/index.php?analysisLink=a04f8f18d4cb2bf01d3aba9844060154
  • 6.
    Figure 1C, H3K4me1neighborhood ● Press on the remove button on the right of Control set Regions ●Press on Neighborhood under H3K4me1 ●(Press on "any" tissue in the figure legend) http://epiexplorer.mpi-inf.mpg.de/index.php?analysisLink=bf53fac474af2214ea81d6c189ba9ac9
  • 7.
    Figure 1D, Predictedgenome elements ●Activate the control set (see Figure 1B, 1/2) ●Press on Chromatin state segmentation http://epiexplorer.mpi-inf.mpg.de/index.php?analysisLink=00b780b85cedb266a306cd04ce83781d
  • 8.
    Figure 1E, DNAmethylation ●Press on to "unlock" the comparison. (After that, every refinement applied to the main dataset will also be applied to the reference. See the dedicated slideshow for more info) ●Press on DNA methylation (ROADMAP) ●Then on hES_H1_p38 ●Then on Number of observed CpGs ●Move the left handle of the slider to 5 ●Press on Filter to this selection ●Press on Average CpG methylation ratio http://epiexplorer.mpi-inf.mpg.de/index.php?analysisLink=13221a5d490ccc3c572281f4ba5e5d9f
  • 9.
    Figure 1F, GeneOntology terms, 1/2 ●Press to remove the Number of CpGs refinement from 1E ●Press to remove the control dataset ●Now, you have reset the dataset to its initial state ●Press on Region score ●Slide the left handle of the slider till 200 ●Press the Filter to this selection button ●Press on Genes and annotations ●Press on Gene ontology (terms) ●Above the visualization, select 50 from the drop-down menu next to "Exclude GO terms matching less than N genes" ●Above the visualization, select 5,100 from the drop-down menu next to "Exclude GO terms matching more than N genes" ●Press twice on the header of the column Ratio
  • 10.
    Figure 1F, GeneOntology terms, 2/2 http://epiexplorer.mpi-inf.mpg.de/index.php?analysisLink=5e950bb28c67d937617b358e910667c5
  • 11.
    This is theend of this presentation. Please check out our other slideshows