NCBoost v2: a classifier for non-coding single nucleotide variants in Mendelian diseases

Authors

Barthélémy Caron (ORCID: https://orcid.org/0000-0002-8373-125X)
Antonio Rausell

Institutions

Inserm (FR)
Université Paris Cité (FR)
Assistance Publique – Hôpitaux de Paris (FR)
Center for Genomic Science (IT)
Institut des Maladies Génétiques Imagine (FR)

Publication Details

Journal: Bioinformatics
Published: 2026-03-23
DOI: https://doi.org/10.1093/bioinformatics/btag138
Primary Topic: Genomics and Rare Diseases
Type: article
Field-Weighted Citation Impact: 0.00

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article

NCBoost v2: a classifier for non-coding single nucleotide variants in Mendelian diseases

Barthélémy Caron, Antonio Rausell

Mar 23, 2026

Bioinformatics

Genomics and Rare Diseases

article

NCBoost v2: a classifier for non-coding single nucleotide variants in Mendelian diseases

Barthélémy Caron, Antonio Rausell

March 23, 2026article en

Abstract

No abstract available for this paper.

Bioinformatics

Inserm (FR), Université Paris Cité (FR), Assistance Publique – Hôpitaux de Paris (FR), Center for Genomic Science (IT), Institut des Maladies Génétiques Imagine (FR)

Zero hunger

Openalex Percentile: Top 7%

Genomics and Rare Diseases

DOI Open Access PDF OpenAlex

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NCBoost v2: a classifier for non-coding single nucleotide variants in Mendelian diseases — Barthélémy Caron, Antonio Rausell · Bioinformatics (2026) | TGRS Research Map | TGRS