Hello, A very similar question came up a few days ago and Jeremy had some good advice for how to approach learning to interpret this data: http://lists.bx.psu.edu/pipermail/galaxy-user/2012-August/004985.html Best, Jen Galaxy team On 8/15/12 8:49 AM, i b wrote:
Dear all, in cuffdiff outputs e.g. transcript differential expression, I find for example: value_1 value_2 log2(fold_change) 7.77183 0 -1.79769e+308
or
value_1 value_2 log2(fold_change) 0 14.5972 1.79769e+308
for many many rows.
if I sort in excel my data by fold change column (big to small ), all the rows with -1.79769e+308 or +1.79769e+308 are on the top. How can be sure that these on the top are really the most up-regulated or down regulated transcripts if I don't know the real value of one of the two samples (is 0 really zero?)? I was told that the zero in one if the two samples is very small number and Cuffdiff simply writes 0, but it is not absolutely zero, otherwise it would not be possible ot have -1.79769e+308 or 1.79769e+308
Could you please tell me then how can I extrapolate the highest fold change? (up and down regualted)?or of what is done by sorting by log fold chnage is correct?
Thanks, ib ___________________________________________________________ The Galaxy User list should be used for the discussion of Galaxy analysis and other features on the public server at usegalaxy.org. Please keep all replies on the list by using "reply all" in your mail client. For discussion of local Galaxy instances and the Galaxy source code, please use the Galaxy Development list:
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