"Benchmark"@en . "Microconversion"@en . "Disease prevalence"@en . "Epidemiology"@en . . "Branch point"@en . <0000-0002-5104-9125> . "Branchpointer"@en . "Molecular genetics"@en . "Minigene splicing assay"@en . "Genotype"@en . "Full-length gene splicing assay"@en . "RNA"@en . "Tau protein"@en . "Genetic variant"@en . . . "RH gene"@en . "Hybrid"@en . . "Prediction"@en . "RNABPS"@en . . "Nonsense-Mediated mRNA Decay"@en . "Yann Fichou" . "Life Sciences"@fr . "Incomplete penetrance"@en . "HSF"@en . "Splice site"@en . "Disease Susceptibility"@en . "Allelic heterogeneity"@en . "Blood group"@en . . "SVM-BPfinder"@en . "Rh"@en . "Human inherited disease"@en . "Pancreatic Acinar Cells"@en . "Yann" . "Variant"@en . "Genetic heterogeneity"@en . "Human Genetics"@en . "Track-etched"@en . "Kinetic"@en . "Sickle cell disease"@en . "Exome sequencing"@en . "Aberrant transcript"@en . "SpliceAI"@en . "Genotype and phenotype relationship"@en . "P301L mutation"@en . "Multifactorial/complex disease"@en . "Fichou" . "Reproductive medicine"@en . "Canonical 5\u2032 splice site"@en . "Human gene mutation database"@en . "Pathogenicity"@en . "Noncanonical splice donor site"@en . "BPP"@en . "Variant interpretation"@en . "Variants"@en . "Genetics"@en . "RHD variants"@en . "f1016b7c0bfb82533eeb3502d8569692" . "Epidemiology genetics RH antigen sickle cell disease variant"@en . "ACMG guidelines"@en . . "Metrics & More Article Recommendations nanopore"@en . "LaBranchoR"@en . "Allele frequency threshold"@en . . "RNA characterisation and manipulation"@en . "Amyloid"@en . "Computational Methods"@en . "Antigens"@en . "Phenotype"@en . "RH antigen"@en . "Heparin-induced aggregation"@en .