Difference between revisions of "Kevinmcgee Week 13"

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(Added pic)
(Added info to journal)
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#Opened [[media:L.infantumCompliedRawData(A).txt | L.infantumCompliedRawData(A).txt]]
+
*Opened [[media:L.infantumCompliedRawData(A).txt | L.infantumCompliedRawData(A).txt]]
#Finished the formatting by flipping the dye swap chips negative
+
*Finished the formatting by flipping the dye swap chips negative
##Created a column next to dye swap chips and did the formula:  
+
*Created a column next to dye swap chips and did the formula:  
##* =-1*(dye swap chip column)
+
=-1*(dye swap chip column)
#made a new sheet
+
*made a new sheet
##added all data from old sheet except only added the flipped dye swaps
+
*added all data from old sheet except only added the flipped dye swaps
#looked for background information in the array paper
+
*looked for background information in the array paper
##L. infantum MHOM/MA/67/ITMAP-263 and L. major LV39 MRHO/SU/59/P strains used in this study
+
**L. infantum MHOM/MA/67/ITMAP-263 and L. major LV39 MRHO/SU/59/P strains used in this study
##All microarray data will be freely available on the Geo NCBI database in the MIAME format
+
**All microarray data will be freely available on the Geo NCBI database in the MIAME format
##*The series accession number for our manuscript is GSE10407.
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***The series accession number for our manuscript is GSE10407.
##Each chip compares promastigote vs. amastigote with different replicates
+
**Each chip compares promastigote vs. amastigote with different replicates
##Following data files found
+
**Following data files found
 
[[File:LmjSampleInfo.PNG]]
 
[[File:LmjSampleInfo.PNG]]
#Finished naming sheet with helpful names to know what is what on the sheet
+
*Finished naming sheet with helpful names to know what is what on the sheet
#Ready for statistical analysis
+
7Ready for statistical analysis
 +
7Began analysis by taking the average and standard deviation of our data chips seperately and using that information to scale and center our data:
 +
=(B4-B$2)/B$3 This shows the equation we used to scale and center.
 +
*Copied and pasted values of scaled centered onto a new page. From there, we edited out all VALUE! cells and left them blank. GenMAPP will ignore these blanks when we input our data.
 +
*Made a column of the average fold change for each gene call Avg_LogFC_All
 +
Average B2:G2
 +
*

Revision as of 18:28, 21 November 2013

  • Opened L.infantumCompliedRawData(A).txt
  • Finished the formatting by flipping the dye swap chips negative
  • Created a column next to dye swap chips and did the formula:
=-1*(dye swap chip column)
  • made a new sheet
  • added all data from old sheet except only added the flipped dye swaps
  • looked for background information in the array paper
    • L. infantum MHOM/MA/67/ITMAP-263 and L. major LV39 MRHO/SU/59/P strains used in this study
    • All microarray data will be freely available on the Geo NCBI database in the MIAME format
      • The series accession number for our manuscript is GSE10407.
    • Each chip compares promastigote vs. amastigote with different replicates
    • Following data files found

LmjSampleInfo.PNG

  • Finished naming sheet with helpful names to know what is what on the sheet

7Ready for statistical analysis 7Began analysis by taking the average and standard deviation of our data chips seperately and using that information to scale and center our data:

=(B4-B$2)/B$3 This shows the equation we used to scale and center.
  • Copied and pasted values of scaled centered onto a new page. From there, we edited out all VALUE! cells and left them blank. GenMAPP will ignore these blanks when we input our data.
  • Made a column of the average fold change for each gene call Avg_LogFC_All
Average B2:G2
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