Literature DB >> 33639937

Detection of gene fusions using targeted next-generation sequencing: a comparative evaluation.

Carina Heydt1, Christina B Wölwer2, Oscar Velazquez Camacho2, Svenja Wagener-Ryczek2, Roberto Pappesch2, Janna Siemanowski2, Jan Rehker2, Florian Haller3, Abbas Agaimy3, Karl Worm4, Thomas Herold4, Nicole Pfarr5, Wilko Weichert5, Thomas Kirchner6, Andreas Jung6, Jörg Kumbrink6, Wolfgang Goering7, Irene Esposito7, Reinhard Buettner2, Axel M Hillmer2, Sabine Merkelbach-Bruse2.   

Abstract

BACKGROUND: Gene fusions represent promising targets for cancer therapy in lung cancer. Reliable detection of multiple gene fusions is therefore essential.
METHODS: Five commercially available parallel sequencing assays were evaluated for their ability to detect gene fusions in eight cell lines and 18 FFPE tissue samples carrying a variety of known gene fusions. Four RNA-based assays and one DNA-based assay were compared; two were hybrid capture-based, TruSight Tumor 170 Assay (Illumina) and SureSelect XT HS Custom Panel (Agilent), and three were amplicon-based, Archer FusionPlex Lung Panel (ArcherDX), QIAseq RNAscan Custom Panel (Qiagen) and Oncomine Focus Assay (Thermo Fisher Scientific).
RESULTS: The Illumina assay detected all tested fusions and showed the smallest number of false positive results. Both, the ArcherDX and Qiagen panels missed only one fusion event. Among the RNA-based assays, the Qiagen panel had the highest number of false positive events. The Oncomine Focus Assay (Thermo Fisher Scientific) was the least adequate assay for our purposes, seven fusions were not covered by the assay and two fusions were classified as uncertain. The DNA-based SureSelect XT HS Custom Panel (Agilent) missed three fusions and nine fusions were only called by one software version. Additionally, many false positive fusions were observed.
CONCLUSIONS: In summary, especially RNA-based parallel sequencing approaches are potent tools for reliable detection of targetable gene fusions in clinical diagnostics.

Entities:  

Keywords:  DNA-Seq; FISH; Gene fusion; NGS; RNA-seq

Year:  2021        PMID: 33639937      PMCID: PMC7912891          DOI: 10.1186/s12920-021-00909-y

Source DB:  PubMed          Journal:  BMC Med Genomics        ISSN: 1755-8794            Impact factor:   3.063


  40 in total

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