Evidence map›Paper›PMID 35696076›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2022

A Pretrained ELECTRA Model for Kinase-Specific Phosphorylation Site Prediction.

Lei Jiang, Duolin Wang, Dong Xu

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Lei JiangDepartment of Electrical Engineering and Computer Science and Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO, USA.
Duolin WangDepartment of Electrical Engineering and Computer Science and Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO, USA.
Dong XuDepartment of Electrical Engineering and Computer Science and Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO, USA. xudong@missouri.edu.

Funding

Multi-view self-supervised deep learning for biological sequences and beyondR35GM126985 · NIGMS · UNIVERSITY OF SOUTH FLORIDA · PI DONG XU · 2018 to 2026
$3.8M
NIGMS NIH HHS R35 GM126985
6 · The paper itself

Abstract

Phosphorylation plays a vital role in signal transduction and cell cycle. Identifying and understanding phosphorylation through machine-learning methods has a long history. However, existing methods only learn representations of a protein sequence segment from a labeled dataset itself, which could result in biased or incomplete features, especially for kinase-specific phosphorylation site prediction in which training data are typically sparse. To learn a comprehensive contextual representation of a protein sequence segment for kinase-specific phosphorylation site prediction, we pretrained our model from over 24 million unlabeled sequence fragments using ELECTRA (Efficiently Learning an Encoder that Classifies Token Replacements Accurately). The pretrained model was applied to kinase-specific site prediction of kinases CDK, PKA, CK2, MAPK, and PKC. The pretrained ELECTRA model achieves 9.02% improvement over BERT and 11.10% improvement over MusiteDeep in the area under the precision-recall curve on the benchmark data.

Indexed as

Machine LearningProtein KinasesPhosphorylationProtein KinasesDeep leaningELECTRAKinase-specific phosphorylation site predictionPhosphorylationPretrainingTransformer

Identifiers

What OpenQuestion holds

Textmetadata
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.