Evidence map›Paper›PMID 41293319›Full record

ArticleBioinformatics advances2025

SiaScoreNet: a siamese neural network-based model integrating prediction scores for HLA-peptide interaction prediction.

Mahsa Saadat, Fatemeh Zare-Mirakabad, Milad Besharatifard

Abstract read
In one paragraph

Article in Bioinformatics advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Mahsa SaadatComputational Biology Research Center (CBRC), Amirkabir University of Technology, Tehran, Iran.ORCID https://orcid.org/0000-0003-1698-5011
Fatemeh Zare-MirakabadComputational Biology Research Center (CBRC), Amirkabir University of Technology, Tehran, Iran.ORCID https://orcid.org/0000-0003-2849-3778
Milad BesharatifardComputational Biology Research Center (CBRC), Amirkabir University of Technology, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: Cancer immunotherapy uses the immune system to recognize and eliminate tumor cells by presenting tumor antigens through Human Leukocyte Antigen (HLA) molecules. Accurate prediction of HLA-peptide interactions is essential for personalized immunotherapy development. Allele-specific models achieve high accuracy and handle variable peptide lengths but require separate training for each allele, limiting scalability to rare or unseen HLAs. Pan-specific models generalize across multiple alleles and match or surpass allele-specific methods. Ensemble methods improve prediction by combining outputs from multiple predictors, often via linear combinations, though nonlinear strategies may better capture HLA-peptide complexities.We propose Results: Benchmark evaluations show Availability and implementation: The data and source code for prediction and experiments presented in this study is publicly available in the

Identifiers

PMID41293319
PMCPMC12641608

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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.