Hi Debanga,
A range as you describe is normal. These values are on a log2 scale, so a SIN 
delta of 1 roughly corresponds to a 2-fold change +/- the variance.
Often the variance can be high for LFQ which makes it challenging to see p < 
0.05 when comparing conditions. Without knowing your exact experimental setup, 
I would suggest sorting from largest to smallest delta SIN and see if those 
proteins make sense biologically. If you need stat. sig. you may eventually 
need to move to a targeted or DIA approach with lower variance.

dSIN and SIN are effectively the same, except dSIN includes algorithms which 
distribute intensity for non unique peptides across the protein group according 
to the evidence for each protein's existence. 

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