Evidence map›Paper›PMID 40838786›Full record

ArticleBriefings in bioinformatics2025

LncPTPred: predicting lncRNA-protein interaction based on crosslinking and immunoprecipitation (CLIP-Seq) data.

Gourab Das, Troyee Das, Zhumur Ghosh

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
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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.

Gourab DasDepartment of Biological Sciences, Bose Institute, Unified Academic Campus, Kolkata 700 091, West Bengal, India.
Troyee DasDepartment of Biological Sciences, Bose Institute, Unified Academic Campus, Kolkata 700 091, West Bengal, India.
Zhumur GhoshDepartment of Biological Sciences, Bose Institute, Unified Academic Campus, Kolkata 700 091, West Bengal, India.ORCID 0000-0002-4877-7551

Funding

Department of Science & Technology, Government of IndiaIndian Council of Medical Research RBMH/FW/2020/10National Network project of Bose Institute with Indian Statistical Institute and Vidyasagar University BT/PR40176/BTIS/137/84/2023
6 · The paper itself

Abstract

Long noncoding RNA (lncRNA)-protein Interaction (LPI) across diverse biological systems, directly and indirectly, regulates various cellular processes. Experimental assays to recognize the protein binding partners of lncRNAs are highly time-consuming and expensive. In silico predictive approaches involving pattern recognition techniques provide a promising alternative to it by reducing the search space. Our work identifies such hidden patterns within the cross-linking immunoprecipitation sequencing (CLIP-Seq) data, which aid in overcoming the problem of obtaining a real negative dataset and thus offer a state-of-the-art machine learning (ML)-based prediction algorithm to predict LPI. The initial phase of this work involves preparing the training dataset, and the next phase is devoted towards developing an ML-based model to perform prediction operations. To demonstrate the efficacy of our model, its performance has been compared to that of contemporary prediction tools, with the result clearly showing the outperformance of our model. Moreover, it also provides the segments of interaction within the lncRNA loci, which act as a roadmap for the precise design of the validation experiment. The LncPTPred tool has been provided in terms of a web server as well as a standalone version on GitHub. Web server Link: http://bicresources.jcbose.ac.in/zhumur/lncptpred/. Github Link: https://github.com/zglabDIB/lncptpred.git.

Indexed as

Computational BiologyRNA-Binding ProteinsRNA, Long NoncodingSoftwareAlgorithmsHumansImmunoprecipitationMachine LearningProtein BindingRNA-Binding ProteinsRNA, Long NoncodingCLIP-Seqhyperparameter optimizationlncRNA–protein interactionmachine learning

Identifiers

PMID40838786
PMCPMC12368852

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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.