MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing

Eitemau Tebyg

• Inferring the molecular and phenotypic impact of amino acid variants with MutPred2
  gan: Pejaver, Vikas, et al.
  Cyhoeddwyd: (2020)
• Exon identity crisis: disease-causing mutations that disrupt the splicing code
  gan: Sterne-Weiler, Timothy, et al.
  Cyhoeddwyd: (2014)
• Loss of exon identity is a common mechanism of human inherited disease
  gan: Sterne-Weiler, Timothy, et al.
  Cyhoeddwyd: (2011)
• New mtDNA Association Model, MutPred Variant Load, Suggests Individuals With Multiple Mildly Deleterious mtDNA Variants Are More Likely to Suffer From Atherosclerosis
  gan: Piotrowska-Nowak, Agnieszka, et al.
  Cyhoeddwyd: (2019)
• Nucleotide substitutions within the cardiac troponin T alternative exon disrupt pre-mRNA alternative splicing.
  gan: Cooper, T A, et al.
  Cyhoeddwyd: (1989)