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Fast and sensitive validation of fusion transcripts in whole-genome sequencing data

BACKGROUND: In cancer, genomic rearrangements can create fusion genes that either combine protein-coding sequences from two different partner genes or place one gene under the control of the promoter of another gene. These fusion genes can act as oncogenic drivers in tumor development and several fu...

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Detalles Bibliográficos
Autores principales:	Hafstað, Völundur, Häkkinen, Jari, Persson, Helena
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2023
Materias:	Software
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518092/ https://www.ncbi.nlm.nih.gov/pubmed/37741966 http://dx.doi.org/10.1186/s12859-023-05489-5

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