ClinPrior: an algorithm for diagnosis and novel gene discovery by network-based prioritization

ClinPrior: an algorithm for diagnosis and novel gene discovery by network-based prioritization

Abstract Background Whole-exome sequencing (WES) and whole-genome sequencing (WGS) have become indispensable tools to solve rare Mendelian genetic conditions. Nevertheless, there is still an urgent need for sensitive, fast algorithms to maximise WES/WGS diagnostic yield in rare disease patients. Mos...

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Main Authors: Agatha Schlüter, Valentina Vélez-Santamaría, Edgard Verdura, Agustí Rodríguez-Palmero, Montserrat Ruiz, Stéphane Fourcade, Laura Planas-Serra, Nathalie Launay, Cristina Guilera, Juan José Martínez, Christian Homedes-Pedret, M. Antonia Albertí-Aguiló, Miren Zulaika, Itxaso Martí, Mónica Troncoso, Miguel Tomás-Vila, Gemma Bullich, M. Asunción García-Pérez, María-Jesús Sobrido-Gómez, Eduardo López-Laso, Carme Fons, Mireia Del Toro, Alfons Macaya, HSP/ataxia workgroup, Sergi Beltran, Luis G. Gutiérrez-Solana, Luis A. Pérez-Jurado, Sergio Aguilera-Albesa, Adolfo López de Munain, Carlos Casasnovas, Aurora Pujol
Format: Article
Language:English
Published: BMC 2023-09-01
Series:Genome Medicine
Subjects:
Algorithm
WES/WGS
HPOs
Variant prioritization
Interactome
Hereditary spastic paraplegia
Online Access:https://doi.org/10.1186/s13073-023-01214-2

Internet

https://doi.org/10.1186/s13073-023-01214-2

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