Dahlquist:Notebook/Microarray Data Analysis/2008/10/14: Difference between revisions

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== Today's Workflow ==
== Today's Workflow ==
* Replace this text with your actual notebook entry (workflow).
* Please sign your notebook entries with your wiki signature:


  <nowiki>~~~~</nowiki>
* First compared dCIN5 and wt data following the same procedure as outlined on 10/02/2008:
 
** Files in Desktop "Data analysis 2008-10-02"
** Used gene file "wt-dCIN5_consolidated_Edge_genes-indexonly_20080715.txt"
** Used covariate file "wt-dCIN5_consolidated_Edge_covariates_20080710.txt
* Load both into an Edge session.
* Select "Impute Missing Data" from the menu.  Calculate Percent Missing Data by clicking on the button. The results are:
** Percent of genes missing data: 7.63%
** Percent of arrays missing data: 95.35%
** Overall percent of missing data: 3.15%
* For KNN Parameters, set:
** Percent of missing values to tolerate in a gene: 100 (so all genes included)
** Number of nearest neighbors to use (maximum of 15): 15
** clicked GO to impute missing data.
* Selected "Identify Differentially Expressed Genes"
** Note: this is to compare between the wt and dCIN5 strains. Different parameters and gene/covariate files will need to be used to analyze individual strains.
** Class Variable is: Strain
** Differential Expression Type is: Time Course
** Number of null iterations, set to 1000
** Choose a seed for reproducible results, set to 47
** Choose Time Course Settings
** Covariate giving time points is: Timepoint
** Covariate corresponding to individuals is: Flask
** Choose spline type, accepted default of Natural Cubic Spline, dimension 4
** Click "Apply" and then click "Go"
** 1000 permutations looks like it will take about 10 minutes.
* Results: (Saved in 2008-10-14 Results)
** No significant genes under these settings.
** Choose Q-Value cutoff as 1, recalculate
** Saved total list of genes as: "20081014_wt_dCIN5_comparison_results_allgenes" in "Data analysis 2008-10-02"
** Saved


which would look like this on the page:  ''&mdash; [[User:Kam D. Dahlquist|Kam D. Dahlquist]] 19:35, 2 October 2008 (EDT)''




Revision as of 12:18, 14 October 2008

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Today's Workflow

  • First compared dCIN5 and wt data following the same procedure as outlined on 10/02/2008:
    • Files in Desktop "Data analysis 2008-10-02"
    • Used gene file "wt-dCIN5_consolidated_Edge_genes-indexonly_20080715.txt"
    • Used covariate file "wt-dCIN5_consolidated_Edge_covariates_20080710.txt
  • Load both into an Edge session.
  • Select "Impute Missing Data" from the menu. Calculate Percent Missing Data by clicking on the button. The results are:
    • Percent of genes missing data: 7.63%
    • Percent of arrays missing data: 95.35%
    • Overall percent of missing data: 3.15%
  • For KNN Parameters, set:
    • Percent of missing values to tolerate in a gene: 100 (so all genes included)
    • Number of nearest neighbors to use (maximum of 15): 15
    • clicked GO to impute missing data.
  • Selected "Identify Differentially Expressed Genes"
    • Note: this is to compare between the wt and dCIN5 strains. Different parameters and gene/covariate files will need to be used to analyze individual strains.
    • Class Variable is: Strain
    • Differential Expression Type is: Time Course
    • Number of null iterations, set to 1000
    • Choose a seed for reproducible results, set to 47
    • Choose Time Course Settings
    • Covariate giving time points is: Timepoint
    • Covariate corresponding to individuals is: Flask
    • Choose spline type, accepted default of Natural Cubic Spline, dimension 4
    • Click "Apply" and then click "Go"
    • 1000 permutations looks like it will take about 10 minutes.
  • Results: (Saved in 2008-10-14 Results)
    • No significant genes under these settings.
    • Choose Q-Value cutoff as 1, recalculate
    • Saved total list of genes as: "20081014_wt_dCIN5_comparison_results_allgenes" in "Data analysis 2008-10-02"
    • Saved



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