Off topic:Understaning of two-color array data
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@firozimtech-16167
Last seen 5.3 years ago

I would be very thankful if you could kindly tell me more about Data table header descriptions of GEO:GSM269939

Following is the Data table header descriptions:

ID_REF Rosetta generated unique probe identifier
VALUE Corrected Log10 Ratio of channels (CH2/CH1)
LOGINTENSITY Corrected average log intensity of channels
INTENSITY1 Intensity of channel1
INTENSITY2 Intensity of channel2
PVALUE P-value of LogRatio
QUALITY 1 - if good and non control, 0 - otherwise

 

Following is the sample data:

ID_REF VALUE LOGINTENSITY INTENSITY1 INTENSITY2 P-VALUE QUALITY
10018172985 -0.1800 -2.0999 0.0102 0.0067 1.4772e-001 1
10018172987 0.0417 -1.0711 0.0858

0.0935

4.2847e-001 1

 

Following are my questions:

  1. INTENSITY 1 and INTENSITY 2 are Cy3(control) and Cyt5 (treatment) and both values are not log (log2 or log10) transformed. I think these intensities are average intensity from different experiments of the same gene ID_REF?
  2.  What is the VALUE (Corrected Log10 Ratio of channels (CH2/CH1))? For probe 10018172987, If I am using log10(0.0935/0.0858) I am getting the value 0.03732432 and not 0.0417 as mentioned in the table.
  3. What is LOGINTENSITY (Corrected average log intensity of channels)? How was it calculated using the INTENSITY 1 and INTENSITY 2?
  4. PVALUE indicates whether Corrected Log10 Ratio of channels (CH2/CH1) is significant or not.
  5. Can I use the INTENSITY 1 (control )and INTENSITY 2 (treatment) as the expression of a gene as like a single-channel gene expression values?

 

Thanks,

F Ahmed

microarray limma two-color microaray • 194 views
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