Exploiting allele-specific transcriptional effects of subclonal copy number alterations for genotype-phenotype mapping in cancer cell populations.
clonal phenotypes
genotype phenotype
single cell DNA
single cell RNA
Journal
bioRxiv : the preprint server for biology
Titre abrégé: bioRxiv
Pays: United States
ID NLM: 101680187
Informations de publication
Date de publication:
17 Jan 2023
17 Jan 2023
Historique:
pubmed:
31
1
2023
medline:
31
1
2023
entrez:
30
1
2023
Statut:
epublish
Résumé
Somatic copy number alterations drive aberrant gene expression in cancer cells. In tumors with high levels of chromosomal instability, subclonal copy number alterations (CNAs) are a prevalent feature which often result in heterogeneous cancer cell populations with distinct phenotypes
Identifiants
pubmed: 36711951
doi: 10.1101/2023.01.10.523464
pmc: PMC9882029
pii:
doi:
Types de publication
Preprint
Langues
eng
Déclaration de conflit d'intérêts
Competing Interests SPS is a shareholder of Imagia Canexia Health Inc. and is a consultant to AstraZeneca Inc., outside the scope of this work.