Evidence map›Paper›PMID 41260881›Full record

ArticleLife science alliance2026

Regulators of homologous recombination deficiency identified by machine learning using somatic multi-omics data.

Renan Valieris, Lucas Rosa, Luan Martins, Alexandre Defelicibus, Dirce Maria Carraro, Diana Noronha Nunes, Emmanuel Dias-Neto, Rafael Rosales, Israel Tojal da Silva

Abstract read
In one paragraph

Article in Life science alliance, 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

9 authors.

Renan ValierisLaboratory of Computational Biology and Bioinformatics, A.C. Camargo Cancer Center, São Paulo, Brazil.ORCID 0000-0002-8402-3175
Lucas RosaClinical and Functional Genomics Group, A.C. Camargo Cancer Center, São Paulo, Brazil.ORCID 0009-0001-8614-4245
Luan MartinsClinical and Functional Genomics Group, A.C. Camargo Cancer Center, São Paulo, Brazil.
Alexandre DefelicibusClinical and Functional Genomics Group, A.C. Camargo Cancer Center, São Paulo, Brazil.
Dirce Maria CarraroClinical and Functional Genomics Group, A.C. Camargo Cancer Center, São Paulo, Brazil.
Diana Noronha NunesDivision of Cancer Biology, Department of Radiation Oncology, Rutgers New Jersey Medical School, Newark, NJ, USA.
Emmanuel Dias-NetoDivision of Cancer Biology, Department of Radiation Oncology, Rutgers New Jersey Medical School, Newark, NJ, USA.
Rafael RosalesDepartamento de Computação e Matemática, Universidade de São Paulo, São Paulo, Brazil.ORCID 0000-0002-7518-2975
Israel Tojal da SilvaLaboratory of Computational Biology and Bioinformatics, A.C. Camargo Cancer Center, São Paulo, Brazil itojal@accamargo.org.br.ORCID 0000-0002-4687-1499

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Homologous recombination deficiency (HRD) is a critical biomarker for guiding targeted therapies, yet the full range of somatic alterations driving HRD across cancers remains incompletely characterized. Here, we present a tumor-agnostic machine learning framework that integrates somatic multi-omics data, including copy-number variations, single-nucleotide variants, DNA methylation, and gene expression from over 8,000 patients in The Cancer Genome Atlas. Using a genome-wide mutational signature-based HRD score as ground truth, our model achieved high predictive performance and leveraged SHAP-based explainability to uncover HRD regulators beyond

Indexed as

Homologous RecombinationMachine LearningNeoplasmsBiomarkers, TumorDNA Copy Number VariationsDNA MethylationGene Expression Regulation, NeoplasticGenomicsHumansMultiomicsMutationPolymorphism, Single NucleotideBiomarkers, Tumor

Identifiers

PMID41260881
PMCPMC12631081

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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.