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Benchmarking splice variant prediction algorithms using massively parallel splicing assays

BACKGROUND: Variants that disrupt mRNA splicing account for a sizable fraction of the pathogenic burden in many genetic disorders, but identifying splice-disruptive variants (SDVs) beyond the essential splice site dinucleotides remains difficult. Computational predictors are often discordant, compou...

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Detalles Bibliográficos
Autores principales: Smith, Cathy, Kitzman, Jacob O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10187268/
https://www.ncbi.nlm.nih.gov/pubmed/37205456
http://dx.doi.org/10.1101/2023.05.04.539398