Evidence map›Paper›PMID 39576583›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Accurate and Fast Prediction of Intrinsic Disorder Using flDPnn.

Kui Wang, Gang Hu, Zhonghua Wu, Lukasz Kurgan

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. 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

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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

4 authors.

Kui WangNITFID, School of Statistics and Data Science, LPMC and KLMDASR, Nankai University, Tianjin, China.
Gang HuNITFID, School of Statistics and Data Science, LPMC and KLMDASR, Nankai University, Tianjin, China.
Zhonghua WuSchool of Mathematical Sciences and LPMC, Nankai University, Tianjin, China.
Lukasz KurganDepartment of Computer Science, Virginia Commonwealth University, Richmond, VA, USA. lkurgan@vcu.edu.

Funding

National Science Foundation DBI2146027National Science Foundation IIS2125218
6 · The paper itself

Abstract

Intrinsically disordered proteins (IDPs) that include one or more intrinsically disordered regions (IDRs) are abundant across all domains of life and viruses and play numerous functional roles in various cellular processes. Due to a relatively low throughput and high cost of experimental techniques for identifying IDRs, there is a growing need for fast and accurate computational algorithms that accurately predict IDRs/IDPs from protein sequences. We describe one of the leading disorder predictors, flDPnn. Results from a recent community-organized Critical Assessment of Intrinsic Disorder (CAID) experiment show that flDPnn provides fast and state-of-the-art predictions of disorder, which are supplemented with the predictions of several major disorder functions. This chapter provides a practical guide to flDPnn, which includes a brief explanation of its predictive model, descriptions of its web server and standalone versions, and a case study that showcases how to read and understand flDPnn's predictions.

Indexed as

AlgorithmsComputational BiologyIntrinsically Disordered ProteinsSoftwareDatabases, ProteinHumansProtein ConformationIntrinsically Disordered ProteinsDeep learningDeep neural networkflDPnnIntrinsically disordered proteinIntrinsic disorderMachine learningPredictionWeb server

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.