Journal of Molecular DiagnosticsBioinformaticsPeer-reviewed journal article
JuLI: accurate detection of DNA fusions in clinical sequencing for precision oncology
Hyun‐Tae ShiniD, Nayoung K. D. KimiD, Jae Won YuniD, Boram LeeiD, Sungkyu Kyung, Ki-Wook Lee, Daeun RyuiD, Jin-Ho KimiD, Joon Seol Bae, Donghyun ParkiD, Yoon‐La ChoiiD, Se‐Hoon LeeiD, Myung‐Ju AhniD, Keunchil ParkiD, Woong‐Yang ParkiD
Abstract
Accurate detection of genomic fusions by high-throughput sequencing in clinical samples with inadequate tumor purity and formalin-fixed paraffin embedded (FFPE) tissue is an essential task in precise oncology. We developed the fusion detection algorithm Junction Location Identifier (JuLI) for optimization of high-depth clinical sequencing. We implemented novel filtering steps to minimize false positives and a joint calling function to increase sensitivity in clinical setting. We comprehensively validated the algorithm using high-depth sequencing data from cancer cell lines and clinical samples and whole genome sequencing data from NA12878. We showed that JuLI outperformed state-of-the-art fusion callers in cases with high-depth clinical sequencing and rescued a driver fusion from false negative in plasma cell-free DNA. JuLI is freely available via GitHub (https://github.com/sgilab/JuLI).
- organism: human
- assay: whole-genome sequencing
- research focus: variant calling
- approach: statistical model
- Citations
- 8
- FWCI
- 0.32
- Field percentile
- 47th percentile
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