Evidence map›Paper›PMID 30135358›Full record

ArticleInternational journal of molecular sciences2018

IDP⁻CRF: Intrinsically Disordered Protein/Region Identification Based on Conditional Random Fields.

Yumeng Liu, Xiaolong Wang, Bin Liu

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Special Protein or RNA Molecules Computational Identification.International journal of molecular sciences · 2023
    Article
  5. Deep learning in prediction of intrinsic disorder in proteins.Computational and structural biotechnology journal · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Yumeng LiuSchool of Computer Science and Technology, Harbin Institute of Technology Shenzhen Graduate School, Shenzhen 518055, Guangdong, China. ymliu.hitsz@gmail.com.
Xiaolong WangSchool of Computer Science and Technology, Harbin Institute of Technology Shenzhen Graduate School, Shenzhen 518055, Guangdong, China. wangxl@insun.hit.edu.cn.
Bin LiuSchool of Computer Science and Technology, Harbin Institute of Technology Shenzhen Graduate School, Shenzhen 518055, Guangdong, China. bliu@hit.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate prediction of intrinsically disordered proteins/regions is one of the most important tasks in bioinformatics, and some computational predictors have been proposed to solve this problem. How to efficiently incorporate the sequence-order effect is critical for constructing an accurate predictor because disordered region distributions show global sequence patterns. In order to capture these sequence patterns, several sequence labelling models have been applied to this field, such as conditional random fields (CRFs). However, these methods suffer from certain disadvantages. In this study, we proposed a new computational predictor called IDP⁻CRF, which is trained on an updated benchmark dataset based on the MobiDB database and the DisProt database, and incorporates more comprehensive sequence-based features, including PSSMs (position-specific scoring matrices), kmer, predicted secondary structures, and relative solvent accessibilities. Experimental results on the benchmark dataset and two independent datasets show that IDP⁻CRF outperforms 25 existing state-of-the-art methods in this field, demonstrating that IDP⁻CRF is a very useful tool for identifying IDPs/IDRs (intrinsically disordered proteins/regions). We anticipate that IDP⁻CRF will facilitate the development of protein sequence analysis.

Indexed as

Models, MolecularProtein Interaction Domains and MotifsAlgorithmsComputational BiologyIntrinsically Disordered ProteinsNeural Networks, ComputerProtein BindingProtein ConformationStructure-Activity RelationshipSupport Vector MachineIntrinsically Disordered Proteinsconditional random fields (CRFs)intrinsically disordered proteins/regionskmerPSSMsrelative solvent accessibilitysecondary structure

Identifiers

PMID30135358
PMCPMC6164615

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.