BIOL368/F14:Chloe Jones Week 13: Difference between revisions

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(note to start from sheet SAR only)
(→‎Calculating fold change: instructions for taking log2)
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*<u>Step. 1</u> Rename the columns with the item isolated, biological replicate, and dye used. For each array data file there will be 2 columns: signal and background.  
*<u>Step. 1</u> Rename the columns with the item isolated, biological replicate, and dye used. For each array data file there will be 2 columns: signal and background.  
*<u>Step. 2</u> Minus the background from the signal for each data file. Then take the answers from each replicate and divide it by its corresponding dye (i.e. Cy5 Ranalexin(B1)/Cy3 MRSA252 (B1)). NOw, the fold change is calculated.
*<u>Step. 2</u> Minus the background from the signal for each data file. Then take the answers from each replicate and divide it by its corresponding dye (i.e. Cy5 Ranalexin(B1)/Cy3 MRSA252 (B1)). NOw, the fold change is calculated.
* Step 3.  Take the log2 of each fold change.
=LOG(number, base)
for example, =LOG(A1,2) takes the log2 of the number in cell A1.

Revision as of 16:01, 19 November 2014

Calculating fold change

  • Here is the Overton_MicroarrayData_20141119.xlsx used for this analysis of MRSA with Ranalexin.
    • Start from the sheet called "SAR_only"
  • Step. 1 Rename the columns with the item isolated, biological replicate, and dye used. For each array data file there will be 2 columns: signal and background.
  • Step. 2 Minus the background from the signal for each data file. Then take the answers from each replicate and divide it by its corresponding dye (i.e. Cy5 Ranalexin(B1)/Cy3 MRSA252 (B1)). NOw, the fold change is calculated.
  • Step 3. Take the log2 of each fold change.
=LOG(number, base)
for example, =LOG(A1,2) takes the log2 of the number in cell A1.