Short-Read Sequencing Detects Large Structural Variants in Cancer Genomes.
Journal
Cancer discovery
ISSN: 2159-8290
Titre abrégé: Cancer Discov
Pays: United States
ID NLM: 101561693
Informations de publication
Date de publication:
22 Nov 2023
22 Nov 2023
Historique:
medline:
22
11
2023
pubmed:
22
11
2023
entrez:
22
11
2023
Statut:
aheadofprint
Résumé
Most large structural variants (SV) can be detected by short-read sequencing (SRS) of cancer genomes.
Identifiants
pubmed: 37991372
pii: 730255
doi: 10.1158/2159-8290.CD-RW2023-186
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
OF1Informations de copyright
©2023 American Association for Cancer Research.