Evidence map›Paper›PMID 42143580›Full record

ArticleProteomics2026

Enabling Variant Proteogenomic Assay Development Through a Peptide Target Selection Pipeline and Web Application.

Constantinos Blidjios, Pallab Bhowmick, Vincent R Richard, Yassene Mohammed, Christoph H Borchers

Abstract read
In one paragraph

Article in Proteomics, 2026. 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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

5 authors.

Constantinos BlidjiosDepartment of Oncology, McGill University, Montreal, Quebec, Canada.
Pallab BhowmickSegal Cancer Proteomics Centre, Jewish General Hospital, Montreal, Quebec, Canada.
Vincent R RichardSegal Cancer Proteomics Centre, Jewish General Hospital, Montreal, Quebec, Canada.
Yassene MohammedSegal Cancer Proteomics Centre, Jewish General Hospital, Montreal, Quebec, Canada.
Christoph H BorchersSegal Cancer Proteomics Centre, Jewish General Hospital, Montreal, Quebec, Canada.

Funding

Fondation De Famille Alvin SegalGenome Canada and Genome Quebec #6567 Borchers_Zahedi_APFSegal McGill Chair in Molecular OncologyTerry Fox Research InstituteWarren Y. Soper Charitable Trust
6 · The paper itself

Abstract

The quantification of key protein variants can guide precision oncology to enable better identification of driver mutations. Bottom-up assays infer parent protein levels through the quantification of surrogate peptides. Assay methods designed for absolute quantification of protein variants, such as multiple reaction monitoring mass spectrometry (MRM-MS), can achieve quantitation with high precision and specificity. Bottom-up approaches rely on proper selection of suitable surrogate proteogenotypic peptide targets to quantify protein variants of interest. To this end, we developed an R-based bioinformatics pipeline to predict and evaluate variant-specific peptides. The workflow generates variant protein sequences from wild-type sequences and mutations encoded in the Human Genome Variation Society (HGVS) recommended nomenclature, performs in-silico tryptic digestion, and identifies both variant and corresponding wild-type peptides. Each peptide is evaluated by 37 selection criteria to determine suitability as MRM targets. To assess the strictness of these criteria, we applied all protein-altering mutations from the NCI-Genomic Data Commons (GDC) and COSMIC to our pipeline. Of the peptides outputted, 5% satisfied all defined criteria, representing the highest confidence candidates for assay development. We developed a database and web application from NCI-GDC generated peptides for searching, filtering, and downloading. Another web application was developed to provide access to our pipeline.

Indexed as

PeptidesProteogenomicsComputational BiologyDatabases, ProteinHumansInternetMass SpectrometryMutationSoftwarePeptidesbioinformatics toolmass spectrometryproteogenomicsvariant peptide databasevariant peptide prediction

Identifiers

PMID42143580
PMCPMC13519388

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.