Evidence map›Paper›PMID 31307006›Full record

ArticleMolecular therapy. Nucleic acids2019

Identification of Intrinsically Disordered Proteins and Regions by Length-Dependent Predictors Based on Conditional Random Fields.

Yumeng Liu, Shengyu Chen, Xiaolong Wang, Bin Liu

Abstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Deep learning in prediction of intrinsic disorder in proteins.Computational and structural biotechnology journal · 2022
    Review
  6. Article
  7. 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

4 authors.

Yumeng LiuSchool of Computer Science and Technology, Harbin Institute of Technology, Shenzhen, Guangdong 518055, China.
Shengyu ChenSchool of Informatics, Computing and Engineering, Indiana University Bloomington, Bloomington, IN 47408, USA.
Xiaolong WangSchool of Computer Science and Technology, Harbin Institute of Technology, Shenzhen, Guangdong 518055, China. Electronic address: wangxl@insun.hit.edu.cn.
Bin LiuSchool of Computer Science and Technology, Harbin Institute of Technology, Shenzhen, Guangdong 518055, China; School of Computer Science and Technology, Beijing Institute of Technology, Beijing 100081, China; Advanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing 100081, China. Electronic address: bliu@bliulab.net.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate identification of intrinsically disordered proteins/regions (IDPs/IDRs) is critical for predicting protein structure and function. Previous studies have shown that IDRs of different lengths have different characteristics, and several classification-based predictors have been proposed for predicting different types of IDRs. Compared with these classification-based predictors, the previously proposed predictor IDP-CRF exhibits state-of-the-art performance for predicting IDPs/IDRs, which is a sequence labeling model based on conditional random fields (CRFs). Motivated by these methods, we propose a predictor called IDP-FSP, which is an ensemble of three CRF-based predictors called IDP-FSP-L, IDP-FSP-S, and IDP-FSP-G. These three predictors are specially designed to predict long, short, and generic disordered regions, respectively, and they are constructed based on different features. To the best of our knowledge, IDP-FSP is the first predictor that combines a sequence labeling algorithm with IDRs of different lengths. Experimental results using two independent test datasets show that IDP-FSP achieves better or at least comparable predictive performance with 26 existing state-of-the-art methods in this field, proving the effectiveness of IDP-FSP.

Indexed as

conditional random fieldsCRFsensemble predictorintrinsically disordered proteins/regionslength-dependent predictors

Identifiers

PMID31307006
PMCPMC6626971

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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.