Talk:Sequence-Based Mutation Analysis Hemochromatosis

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Revision as of 20:34, 18 June 2012 by Boidolj (talk | contribs)

@PKU (who I think review us this week):
I've tried to keep the DSSP/PsiPred prediction section short as I know you don't like too much "raw output" on the wiki. Is this amount okay with you?^^

  • You could have left out the non-relevant rows of the PSSM also. :-P.
    No, I think it is very good as it is, very little to say, really. The big pictures of the alignment are a little.. overwhelming and there might be redundant sequences in the alignment (hard to check). Maybe a weighting of the methods would improve your results, and I personally think that e.g. the PAM-score is not as significant as a ' proper ' prediction, but I don't have a handy weighting scheme either and understand your decision. Out of curiosity (didn't do it ourselves): How long does SNAP need to make all ~6000 predictions?
  • differ in most predictions but --> differ in most except/but for
    The to be analysed mutations are highlighted. --> The mutations to be analysed are highlighted.
    I think.

Boidolj 18:18, 18 June 2012 (UTC)