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Please use this identifier to cite or link to this item: https://wslhd.intersearch.com.au/wslhdjspui/handle/1/6947
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dc.contributor.authorDorney, R.-
dc.contributor.authorDhungel, B. P.-
dc.contributor.authorRasko, J. E. J.-
dc.contributor.authorHebbard, Lionel-
dc.contributor.authorSchmitz, U.-
dc.date.accessioned2023-06-05T06:12:59Z-
dc.date.available2023-06-05T06:12:59Z-
dc.date.issued2023-
dc.identifier.citationBriefings in Bioinformatics 24(1):19, 2023-
dc.identifier.urihttps://wslhd.intersearch.com.au/wslhdjspui/handle/1/6947-
dc.description.abstractExtensive investigation of gene fusions in cancer has led to the discovery of novel biomarkers and therapeutic targets. To date, most studies have neglected chromosomal rearrangement-independent fusion transcripts and complex fusion structures such as double or triple-hop fusions, and fusion-circRNAs. In this review, we untangle fusion-related terminology and propose a classification system involving both gene and transcript fusions. We highlight the importance of RNA-level fusions and how long-read sequencing approaches can improve detection and characterization. Moreover, we discuss novel bioinformatic tools to identify fusions in long-read sequencing data and strategies to experimentally validate and functionally characterize fusion transcripts.-
dc.titleRecent advances in cancer fusion transcript detection-
dc.typeJournal Article-
dc.identifier.doihttps://dx.doi.org/10.1093/bib/bbac519-
dc.subject.keywordsNeoplasms-
dc.subject.keywordsComputational Biology-
dc.subject.keywordsGene Fusion-
dc.identifier.journaltitleBriefings in Bioinformatics-
dc.identifier.pmid36527429-
dc.contributor.wslhdHebbard, Lionel-
dc.identifier.facilityWestmead-
Appears in Collections:Westmead Hospital 2019 - 2024

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