Evidence map›Paper›PMID 26230689›Full record

ArticleInternational journal of molecular sciences2015

DeepCNF-D: Predicting Protein Order/Disorder Regions by Weighted Deep Convolutional Neural Fields.

Sheng Wang, Shunyan Weng, Jianzhu Ma, Qingming Tang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.1field-weighted citation impact, top 6% of its field
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

32 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Deep learning in prediction of intrinsic disorder in proteins.Computational and structural biotechnology journal · 2022
    Review
  9. Explainable deep neural networks for novel viral genome prediction.Applied intelligence (Dordrecht, Netherlands) · 2022
    Article
  10. Diverse Scientific Benchmarks for Implicit Membrane Energy Functions.Journal of chemical theory and computation · 2021
    Article
  11. Article
  12. Review
  13. Predicting the Real-Valued Inter-Residue Distances for Proteins.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2020
    Article
  14. RDbBMC bioinformatics · 2020
    Article
  15. Article
  16. Review
  17. Article
  18. DISOselect: Disorder predictor selection at the protein level.Protein science : a publication of the Protein Society · 2020
    Article
  19. Article
  20. 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 at 3 institutions in 2 countries.

Sheng WangDepartment of Human Genetics, University of Chicago, Chicago, IL 60637, USA. wangsheng@uchicago.edu.
Shunyan WengMoE Key Laboratory of Developmental Genetics and Neuropsychiatric Diseases, Bio-X Center, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai 200240, China. wengshunyan@hotmail.com.
Jianzhu MaToyota Technological Institute at Chicago, Chicago, IL 60637, USA. majianzhu@gmail.com.
Qingming TangToyota Technological Institute at Chicago, Chicago, IL 60637, USA. tqm2004@gmail.com.
Toyota Technological Institute at Chicago · USShanghai Jiao Tong University · CNUniversity of Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intrinsically disordered proteins or protein regions are involved in key biological processes including regulation of transcription, signal transduction, and alternative splicing. Accurately predicting order/disorder regions ab initio from the protein sequence is a prerequisite step for further analysis of functions and mechanisms for these disordered regions. This work presents a learning method, weighted DeepCNF (Deep Convolutional Neural Fields), to improve the accuracy of order/disorder prediction by exploiting the long-range sequential information and the interdependency between adjacent order/disorder labels and by assigning different weights for each label during training and prediction to solve the label imbalance issue. Evaluated by the CASP9 and CASP10 targets, our method obtains 0.855 and 0.898 AUC values, which are higher than the state-of-the-art single ab initio predictors.

Indexed as

SoftwareIntrinsically Disordered ProteinsSequence Analysis, ProteinIntrinsically Disordered Proteinsconditional neural fielddeep convolutional neural networkdeep learningintrinsically disordered proteinsmachine learningprediction of disordered regions

Identifiers

PMID26230689
PMCPMC4581195
OpenAlexW1864564002

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.