A low computational complexity scheme for the prediction of intrinsically disordered protein regions (Q1721472): Difference between revisions
From MaRDI portal
Changed an Item |
Set OpenAlex properties. |
||
(3 intermediate revisions by 2 users not shown) | |||
Property / describes a project that uses | |||
Property / describes a project that uses: FoldUnfold / rank | |||
Normal rank | |||
Property / describes a project that uses | |||
Property / describes a project that uses: FoldIndex / rank | |||
Normal rank | |||
Property / MaRDI profile type | |||
Property / MaRDI profile type: MaRDI publication profile / rank | |||
Normal rank | |||
Property / full work available at URL | |||
Property / full work available at URL: https://doi.org/10.1155/2018/8087391 / rank | |||
Normal rank | |||
Property / OpenAlex ID | |||
Property / OpenAlex ID: W2795402036 / rank | |||
Normal rank |
Latest revision as of 19:51, 19 March 2024
scientific article
Language | Label | Description | Also known as |
---|---|---|---|
English | A low computational complexity scheme for the prediction of intrinsically disordered protein regions |
scientific article |
Statements
A low computational complexity scheme for the prediction of intrinsically disordered protein regions (English)
0 references
8 February 2019
0 references
Summary: We employ the Rayleigh entropy maximization to develop a novel IDP scheme which requires computing only five features for each residue of a protein sequence, that is, the Shannon entropy, topological entropy, and the weighted average values of three propensities. Furthermore, our scheme is a linear classification method and hence requires computing simpler decision curves which are more robust as well as using fewer learning samples to compute. The simulation results of our scheme as well as some existing schemes demonstrate its effectiveness.
0 references