Network medicine-based epistasis detection in complex diseases: ready for quantum computing.
Journal
medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986
Informations de publication
Date de publication:
09 Nov 2023
09 Nov 2023
Historique:
medline:
11
12
2023
pubmed:
11
12
2023
entrez:
11
12
2023
Statut:
epublish
Résumé
Most heritable diseases are polygenic. To comprehend the underlying genetic architecture, it is crucial to discover the clinically relevant epistatic interactions (EIs) between genomic single nucleotide polymorphisms (SNPs)
Identifiants
pubmed: 38076997
doi: 10.1101/2023.11.07.23298205
pmc: PMC10705612
pii:
doi:
Types de publication
Preprint
Langues
eng