Evidence map›Paper›PMID 41065408›Full record

ArticleBioinformatics (Oxford, England)2026

ImmunoPepper: extracting personalized peptides from complex splicing graphs.

Laurie Prélot, Jiayu Chen, Matthias Hüser, André Kahles, Gunnar Rätsch

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Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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5 authors.

Laurie PrélotDepartment of Computer Science, ETH Zürich, Zürich 8092, Switzerland.ORCID 0000-0001-7063-5333
Jiayu ChenDepartment of Computer Science, ETH Zürich, Zürich 8092, Switzerland.
Matthias HüserDepartment of Computer Science, ETH Zürich, Zürich 8092, Switzerland.ORCID 0000-0001-6397-1689
André KahlesDepartment of Computer Science, ETH Zürich, Zürich 8092, Switzerland.ORCID 0000-0002-3411-0692
Gunnar RätschDepartment of Computer Science, ETH Zürich, Zürich 8092, Switzerland.ORCID 0000-0001-5486-8532

Funding

Common Fund of the Office of the Director of the National Institutes of HealthETH core funding PHRT106 /SPHN017DRI19LOOP ZürichNCINHGRINHLBINIDANIMHNINDSSwiss Molecular Pathology Breakthrough Platform (SOCIBP)Swiss Molecular Pathology Breakthrough Platform (SOCIBP) PHRT106 /SPHN017DRI19The LOOP Zurich and the "Monique Dornonville de la Cour-Stiftung"
6 · The paper itself

Abstract

motivationRNA sequencing enables the characterization of a cell's transcript isoforms in healthy and disease conditions. In the context of cancer, local transcript variability may translate to splicing-derived tumor-associated peptides recognized by the immune system. A software tool that extracts such candidate peptides, is of great interest for personalized cancer therapy.

resultsWe present the open-source software tool ImmunoPepper, which extracts a set of biologically plausible peptides from a splicing graph, derived from a set of RNA-seq datasets. This peptide set can be personalized with germline and somatic variation and takes novel RNA splice variants into account. ImmunoPepper supports several filtering options, including subtraction of normal tissue background, prediction of MHC-binding affinity, as well as MassSpec-based validation of identified peptides. We analyzed 32 ovarian cancer (TCGA-OV) and 31 breast invasive carcinoma (TCGA-BRCA) samples, with a strict cancer-specific filtering configuration, and obtained on average 834 and 569 cancer-specific predicted MHC-I binding 9-mers per sample, for each cohort, respectively. MassSpec validation with the target-decoy competition Subset-Neighbor-Search (SNS) showed an average validation rate of 4.5% per TCGA-OV sample and 5.3% per TCGA-BRCA sample. This corresponded to 25 MHC-I binders 9-mers per TCGA-OV sample, and 20 MHC-I binders 9-mers per TCGA-BRCA sample in average. Finally, we draw conclusions about the best framework for generation of splicing-derived neoepitopes and recommend to use joint data structures when processing homogeneously a cancer and a normal cohort and to focus on reproducibility of the candidates across generation pipelines. AVAILABILITY AND IMPLEMENTATION: ImmunoPepper is implemented in Python 3 and is available as open-source software at https://github.com/ratschlab/immunopepper. The online documentation can be found at https://immunopepper.readthedocs.io/en/latest/.

Indexed as

PeptidesSoftwareBreast NeoplasmsFemaleHumansOvarian NeoplasmsPrecision MedicineSequence Analysis, RNAPeptides

Identifiers

PMID41065408
PMCPMC12777967

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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.