Multimodal learning of noncoding variant effects using genome sequence and chromatin structure

MOTIVATION: A growing amount of noncoding genetic variants, including single-nucleotide polymorphisms, are found to be associated with complex human traits and diseases. Their mechanistic interpretation is relatively limited and can use the help from computational prediction of their effects on epig...

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Detalles Bibliográficos
Autores principales: Tan, Wuwei, Shen, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502240/
https://www.ncbi.nlm.nih.gov/pubmed/37669132
http://dx.doi.org/10.1093/bioinformatics/btad541

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502240/
https://www.ncbi.nlm.nih.gov/pubmed/37669132
http://dx.doi.org/10.1093/bioinformatics/btad541

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