Evidence map›Paper›PMID 37258917›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

NetCleave: An Open-Source Algorithm for Predicting C-Terminal Antigen Processing for MHC-I and MHC-II.

Roc Farriol-Duran, Marina Vallejo-Vallés, Pep Amengual-Rigo, Martin Floor, Víctor Guallar

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Article in Methods in molecular biology (Clifton, N.J.), 2023. 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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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

3 citing papers in PubMed.

  1. Article
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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

5 authors.

Roc Farriol-DuranBarcelona Supercomputing Center (BSC), Barcelona, Spain.
Marina Vallejo-VallésBarcelona Supercomputing Center (BSC), Barcelona, Spain.
Pep Amengual-RigoBarcelona Supercomputing Center (BSC), Barcelona, Spain.
Martin FloorBarcelona Supercomputing Center (BSC), Barcelona, Spain.
Víctor GuallarBarcelona Supercomputing Center (BSC), Barcelona, Spain. victor.guallar@bsc.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T cell epitopes presented on the surface of mammalian cells are subjected to a complex network of antigen processing and presentation. Among them, C-terminal antigen processing constitutes one of the main bottlenecks for the generation of epitopes, as it defines the C-terminal end of the final epitope and delimits the peptidome that will be presented downstream. Previously (Amengual-Rigo and Guallar, Sci Rep 111(11):1-8, 2021), we demonstrated that NetCleave stands out as one of the best algorithms for the prediction of C-terminal processing, which in its turn can be crucial to design peptide-based vaccination strategies. In this chapter, we provide a pipeline to exploit the full capabilities of NetCleave, an open-source and retrainable algorithm for predicting the C-terminal antigen processing for the MHC-I and MHC-II pathways.

Indexed as

Antigen PresentationEpitopes, T-LymphocyteAlgorithmsAnimalsMammalsEpitopes, T-LymphocyteAntigen processingBioinformaticsEpitope predictorHLAImmune systemImmunoinformaticsMHC-IMHC-IINeural networksT cells

Identifiers

What OpenQuestion holds

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Registered trials

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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.