Abstract:Prediction of intrinsic disordered proteins is a hot area in the field of bio-information. Due to the high cost of evaluating the disordered regions of protein sequences using experimental methods, we used a low-complexity prediction scheme. Sequence complexity is used in this scheme to calculate five features for each residue of the protein sequence, including the Shannon entropy, the Topo-logical entropy, the Permutation entropy and the weighted average values of two propensities. Particularly, this is the f… Show more
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